key: cord-0717383-0bb96phl
authors: Schütz, Clarissa S.; Stope, Matthias B.; Bekeschus, Sander
title: H2A.X Phosphorylation in Oxidative Stress and Risk Assessment in Plasma Medicine
date: 2021-12-13
journal: Oxid Med Cell Longev
DOI: 10.1155/2021/2060986
sha: 1960ed7ed9d97591d4744da6db31f7a20d9a56b0
doc_id: 717383
cord_uid: 0bb96phl

At serine(139)-phosphorylated gamma histone H2A.X (γH2A.X) has been established over the decades as sensitive evidence of radiation-induced DNA damage, especially DNA double-strand breaks (DSBs) in radiation biology. Therefore, γH2A.X has been considered a suitable marker for biomedical applications and a general indicator of direct DNA damage with other therapeutic agents, such as cold physical plasma. Medical plasma technology generates a partially ionized gas releasing a plethora of reactive oxygen and nitrogen species (ROS) simultaneously that have been used for therapeutic purposes such as wound healing and cancer treatment. The quantification of γH2A.X as a surrogate parameter of direct DNA damage has often been used to assess genotoxicity in plasma-treated cells, whereas no sustainable mutagenic potential of the medical plasma treatment could be identified despite H2A.X phosphorylation. However, phosphorylated H2A.X occurs during apoptosis, which is associated with exposure to cold plasma and ROS. This review summarizes the current understanding of γH2A.X induction and function in oxidative stress in general and plasma medicine in particular. Due to the progress towards understanding the mechanisms of H2A.X phosphorylation in the absence of DSB and ROS, observations of γH2A.X in medical fields should be carefully interpreted.

Since phosphorylated gamma histone H2A.X (γH2A.X) occurs rapidly, abundant, and stoichiometrically with the frequency of DNA double-strand breaks (DSBs), γH2A.X has proven itself as a recognized indicator for radiationinduced DSBs in particular and direct DNA damage in general [1] . Proceeding from this proportionality in radiobiology, γH2A.X was used as a DNA-associated biomarker and a direct correlate of DSBs in different studies testing chemical and physical treatments, for instance, in the field of oncology [2, 3] .

In addition to the oxidative, via reactive oxygen species-(ROS-) induced DNA damage response (DDR), cold physical plasma presents an innovative, promising concept in antitumor therapy [4] [5] [6] . A multicomponent system, cold plasma consists of physical emitters, such as ultraviolet (UV) and thermal radiation, and biological-chemical components, including charged particles and various reactive oxygen and nitrogen species (ROS/RNS) [7] . The anticancer effect of medically accredited plasma jet devices [8] has already been proven to a limited extent in small cohort studies in clinical settings of palliation and precancerous [9] [10] [11] . Accompanying plasma-induced apoptosis, phosphorylation of H2A.X was observed in an array of in vitro studies [12] [13] [14] [15] [16] [17] [18] [19] [20] [21] [22] [23] [24] [25] [26] [27] [28] [29] [30] [31] . These findings led to the hypothesis that direct (oxidative) damage of DNA results from plasma-generated primary ROS [32] . However, in terms of its cellular effect, cold plasma is confirmed as nongenotoxic and nonmutagenic as studies in vitro, in vivo, and long-term follow-up patients suggest [33] [34] [35] [36] . This apparent difference calls for a closer look at γH2A.X in cold plasma treatment, where ROS/RNS are generated extracellularly in contrast to known mutagenic agents such as UV and ionizing radiation (IR) generating radicals directly at the DNA.

Cell metabolism, oxidative stress, DNA damage, and apoptosis are often closely related to H2A.X phosphorylation and have not yet been sufficiently investigated independently to characterize the γH2A.X induction as a function of the plasma treatment. For instance, the cytostatic drug doxorubicin induces DSBs and ROS-mediated oxidative stress leading to H2A.X phosphorylation [37] . As shown in numerous studies, damaged DNA and phosphorylated H2A.X correlate. However, this only applies unidirectionally: every DSB results in H2A.X phosphorylation. Yet, the reverse conclusion that every γH2A.X can be traced back to the presence of a DNA DSB is not permissible [38, 39] . Several studies postulate the cause-effect-consequence relationship that primary ROS (cause), generated exogenously after cold plasma treatment, induce DNA damage directly (effect) marked by nuclear γH2A.X (consequence) [13, 15, 20, 25, 32] . Questionable about this causal relationship is whether plasma-mediated ROS after diffusion through the cell membrane, cytosol, and membranes of endoplasmic reticulum (ER) and the nucleus-not to mention the numerous antioxidant enzymes with exceedingly high rate constants towards ROS [40] -are still able to reach DNA to mediate damage directly. Since, apart from the H2A.X phosphorylation, there is no evidence of cold plasma-associated cytogenetic and intranuclear DNA damage, further clarification of the molecular mechanisms on cells and the γH2A.X induction is required to assess the suitability γH2A.X in plasma medical research.

2. Histone γH2A.X 2.1. Biochemistry. In eukaryotic nuclei, the DNA and DNAbinding proteins and histones form nucleosomes as functional units of the higher-level chromatin complexes ( Figure 1 ) [41] . The crystallographic structure of such a nucleosome comprises 145 to 147 base pairs (bp) of DNA [42] , wound as a superhelix around a histone octamer composed of heterodimers from each of the four histone families: H2A, H2B, H3, and H4. Two tetramers, (H2A-H2B) 2 and (H3-H4) 2 , form the nucleosome core particle [43, 44] . Several genes encode the histones of each family expressed as cell cycle-dependent during DNA replication in the S phase [45] . The histone family H2A as an essential component of chromatin is divided into the members H2A.1-H2A.2, H2A.X, and H2A.Z, of which H2A.1-H2A.2 take the central part [46] . In eukaryotes, H2A.Z represents about 10% of the H2A, H2A.X 2-10% in mammals, and larger fractions up to 25% in lower eukaryotes [2] .

H2A.X consists of its primary structure of 142 amino acids and differs from the remaining members of the H2A family by a highly conserved 22 amino acid sequence at the C-terminus, called KATQAS * QEY-COOH, which is not related to any known domain in vertebrate histone H2A [43] . Within the tetrapeptide Ser 139 -Gln 140 -Glu 141 -Tyr 142 of the S * QEY-motif, histone H2A.X is posttransla-tionally modified. H2A.X can be phosphorylated Cterminally at position serine 139 via an ester bond between a phosphate residue and the hydroxyl group (-OH) and is then called γH2A.X [44] . This phosphorylation as an early DDR component is catalyzed by the phosphotransferases ataxia telangiectasia mutated (ATM), the ataxia telangiectasia, and Rad3-related protein (ATR), and the DNAdependent protein kinase, catalytic subunit (DNA-PKcs) [47, 48] . As serine/threonine kinases, all three of them belong to the phosphoinositide 3-kinases (PI3K). Moreover, mitogen-activated protein kinases (MAPK) p38 and JNK are associated with the formation of γH2A.X [49] [50] [51] . PI3K and p38-MAPK are both activated by DNA lesions. Being imperative for a signaling system to perform, it must be possible to switch off the corresponding signals. For this, the H2A.X phosphorylation is reversed by the protein phosphatases PP2A, PP4C, and PP6 and the wild-type p53-induced phosphatase 1 (WIP1) [52, 53] .

Living organisms are continuously exposed to a wide range of different DNA-damaging agents, affecting health, disease, mutagenesis, and malicious transformation up to cell death. In particular, tumor cells are often deficient in the DDR, so several antitumor therapies are based on the induction of genotoxicity [54] . While DNA single-strand breaks (SSBs) occur 50.000 times per human cell and day, oxidative base damage is less frequent at about 2.000, and intrastrand cross-links and DSBs occur ten times per day [55] . For instance, direct DNA damage is caused by exogenous factors like UV and ionizing radiation, or ROS produced intracellularly by metabolic processes. A variety of repair mediators are integrated into the DNA damage-induced cascade, such as p53 binding protein 1 (53BP1), the tumor suppressor gene product BReast CAncer (BRCA1), ATRIP, KU70/80, and NBS1/Mre11/Rad50 [56] [57] [58] . UVB light-emitting radiation between 290 and 315 nm modifies DNA directly by cross-linking between C and T or between two T bases inducing cyclobutenepyrimidine dimers (CPD) by forming 6-4 photoproducts and inducing DNA single-strand breaks [59] . The SSB repair mechanism is orchestrated by the signaling complex ATR and ATRIP [56] [57] [58] . Ionizing radiation is one of the first exogenous agents involved in DSB induction. In response to a radiation-induced DSB, NBS1, Mre11, and Rad50 accumulate and colocalize with ATM and phosphorylated H2A.X [47] . A well-known mechanism upstream of the signaling cascade leading to the phosphorylation of H2A.X is the autophosphorylation of an ATM monomer at serine 1981 as a result of a DSB [60] . Moreover, the DSB signaling pathway by DNA-PKcs is associated with the protein complex KU70/80 [47] . In one cell cycle, at least 5.000 SSBs are formed caused by endogenous ROS production, and overlapping SSBs lead to DSB formation [39] . Approximately 1% of single-strand breaks are transformed into doublestrand breaks, while 99% are repaired impressively, reflecting the importance and efficiency of the cells' DDR system to protect the DNA [61] . As a cellular response to detected DNA damage, a signaling transduction cascade follows in which the cell can be arrested temporarily via checkpoint 2

Oxidative Medicine and Cellular Longevity control activation and permanently by senescence in the cell cycle or in which cell death can be promoted [62] . While PI3K activation initially appears in response to a large number of DNA damage, phosphorylated H2A.X is instead responsible for the association of repair enzymes and signaling molecules, highlighting its diverse and pleiotropic function [57] .

Roles. In addition to its functional role in the nucleosome to ensure genomic stability, (γ)H2A.X has a specialized cellular function by signaling and initializing DNA repair [47, 62, 63] . The H2A.X phosphorylation is considered one of the first reactions in the cellular DDR, particularly to DNA DSBs, which are among the DNA lesions with the most pronounced cytotoxicity [64, 65] . γH2A.X has already been used as an indicator of apoptosis by chemotherapeutic agents and an early marker for DSBs in human lung adenocarcinoma cells A549 upon exposure to tobacco smoke [61, 66, 67] . The γH2A.X foci test was reported to identify DNA-damaging agents with the same specificity as the in vitro genotoxicity study standard, the cytokinesis-block micronucleus (MN) assay [68] . In addition to MN formation and mutation frequency, the phosphorylation of H2A.X was defined as one of three genotoxic endpoints. As a de novo modification of the histone H2A.X, γH2A.X has a greater degree of reliability in marking DSBs than other repair proteins present intracellularly even without a DNA lesion, such as 53BP1 [69] . The detection of H2A.X phosphorylation has a great potential in evaluating oncological therapeutic approaches in chemotherapy and radiation therapy. Phosphorylated H2A.X, more precisely the loss of γH2A.X, is suggested as an indicator of radio sensitivity [38, 70, 71] .

The formation of γH2A.X is not limited to exposure to ionizing radiation [38] . Several other exogenous noxae lead to H2A.X phosphorylation. Physical factors include UV radiation, low pH, heat, and hypoxia [72] [73] [74] [75] . Chemical toxins include DNA-damaging agents such as bleomycin, doxorubicin, and ROS [37] . Even without exogenous noxae, γH2A.X is formed during somatic V(D)J recombination to facilitate antibody variability in B cells or during DNA replication [76, 77] . As part of DNA fragmentation, γH2A.X is integrated into apoptosis, as apoptotic cells are γH2A.X-positive per se [14, 78] . Additionally, phosphorylated H2A.X acts as a tumor suppressor [62] . When employed as a biodosimeter, H2A.X phosphorylation also has relevance in aging research [79] . DSBs accumulate in senescent cells so that γH2A.X acts as an age marker. In turn, and even in the absence of a DSB, phosphorylated H2A.X occurs in mitotic sex chromosomes to form a condensed chromatin domain, the XY body [80] . In cancer research, quantifying γH2A.X evaluates not only the therapy's effectiveness but also has the potential to detect precancerous lesions and to be a prognostic marker of tumor entities [57, 81, 82] . Here, the γH2A.X level reflects cancer-associated genomic instability of the nuclei [83] . 

In addition to those pleiotropic roles, recent research suggests that the function of γH2A.X is dispensable for the recruitment of DDR enzymes [84] . Neither the initial marking of a DSB nor the initial migration of repair mediators is canceled by the lack of phosphorylated H2A.X so that γH2A.X deficiency does not seem to be deleterious. Phosphorylated H2A.X is said to connect the DDR and ROS signaling pathways [85] . Furthermore, both cascades are involved in apoptosis induction as a consequence of DNA damage. Here, DNA damage-associated γH2A.X regulates Rac1/NOX1-mediated increase in intracellular ROS concentration [86] . A growing body of evidence supports the assumption that γH2A.X occurrence in correlation or noncorrelation with DNA lesions is far more complex. Generally, low quantities of H2A.X phosphorylation are not associated with DNA DSBs [87] . Furthermore, γH2A.X level increase in untreated, normally proliferating cells when entering cell cycle mitosis (M phase) in the absence of a DNA-damaging agent and consequently any induction of a DDR [88] . This apparently suggests a physiological role of γH2A.X apart from DNA damage. In nonstressed cells, downregulation of H2A.X expression leads to damage in the mitochondria [89] . Moreover, the number of γH2A.X foci in apoptotic cells is ten times higher than in nonapoptotic counterparts [90] . Ultimately, there are reports that ROS are responsible for γH2A.X induction so that phosphorylated H2A.X fulfills a potential role in redox signaling [60] .

3.1. γH2A.X Kinetics. The formation of DSBs in tumor cell DNA of tumor tissue is one of the detrimental effects of ionizing radiation, resulting in cell death. Being a biodosimeter in radiobiology, H2A.X is modified within minutes proportionally to the IR intensity, and approximately 1% of all H2A.X proteins is phosphorylated per gray irradiation [91] . One gray induces 35 DSBs per 6 × 10 9 bp of DNA in the G1 phase of the cell cycle, leading to H2A.X phosphorylation distributed over 1% of the chromatin. According to this, about 0.03% of the chromatin, corresponding to 2 × 10 6 bp of DNA, are involved per DSB. Immunocytochemically, γH2A.X can be explored using a phosphor-specific antibody targeting the phosphorylation of the C-terminal serine 139 in the form of so-called γH2A.X foci [39, 92, 93] . It is well observed that the number of foci and radiationinduced DSBs are linked in a one-to-one manner so that the γH2A.X assay is a validated tool for examining the correlation between the absorbed dose and biological effect in radiobiology [38, 47, 94] .

It needs to be emphasized that phosphorylated H2A.X should not be equated with γH2A.X foci. As a DDR component, H2A.X molecules are phosphorylated, flanking DNA damage sites. These domains with a local increase in the levels of phosphorylated H2A.X can be detected by immunofluorescence as γH2A.X foci [95] . Using different assays in cell biology, quantification of phosphorylated H2A.X is often based on fluorescence read-out systems [39] , and γH2A.X measurements exhibit a wide range of numbers, sizes, and levels of phosphorylation [87] . While γH2A.X foci visualized as bright dots in the nucleus are more specific to DSBs, phosphorylated H2A.X respectively dim γH2A.X foci are also observed in untreated cells. Notably, the H2A.X phosphorylation level includes the DNA damage sites and free form of γH2A.X if measured by global methods such as flow cytometry and western blotting. Hence, different findings might be obtained when comparing total vs. nuclear γH2A.X levels, depending on the method used. Methods other than nuclear foci counting may tend to overestimate γH2A.X levels related to DSBs. Moreover, a constitutive background expression of γH2A.X gradually increases with cell aging towards senescence [96] , while especially tumor cells express high endogenous levels, labeled as cryptogenic γH2A.X [97, 98] . In addition, constitutive γH2A.X levels are cell line and treatment agent-dependent [87] , and foci formation and spreading at DNA damage sites is not static but dynamic [99, 100] . This is because foci expand over time so that many foci of lesser intensity generate approximately the same signal as a few intense ones. Thus, potential pitfalls to consider when troubleshooting γH2A.X investigations are foci expansion with time, high background staining, or cytoplasmatic staining for phosphorylated H2A.X. It was estimated that the relation of DNA damage-representing γH2A.X foci and nonfoci-labeled γH2A.X is 1 to 10 to up to 1 to 20 in untreated cells [39] . This also applies to UV radiation [101] and should be carefully considered when analyzing γH2A.X. However, the agent-and dosedependent nuclear-to-cytoplasmic ratio can be reversed, e.g., with IR [102] . Particularly for low doses, nuclear γH2A.X foci represent the overall staining intensity well, while high doses may induce more pronounced cytoplasmic foci staining. Adding to this complexity, a uniform widespread nuclear H2A.X phosphorylation (pan-nuclear γH2A.X) pattern can be observed especially in cells succumbing to replication stress [103] .

Because the response of eukaryotic cells to ionizing radiation is highly conserved and mediated by a DNA repair system characterized by early H2A.X phosphorylation, the γH2A.X foci detection is a wellestablished and sensitive assay to evaluate persistent DNA DSBs [70, 104] . Discussions on genotoxicological studies emphasized that phosphorylated H2A.X has potential in the clinical setting, in particular, to determine the extent of DNA damage in patients undergoing radiotherapy [105] . However, radiation therapy is a modality of anticancer therapy and is vital in diagnostics, such as computer tomography. Hence, the investigation of γH2A.X adjacent to the DSB is of great relevance [106] . In cell lines in vitro, phosphorylation of H2A.X is a measure of radiosensitivity [107, 108] . Fast loss and less retention of γH2A.X are therefore associated with increased radioresistance [38] . Hence, radiosensitive tumor cell lines retain phosphorylated H2A.X longer than radioresistant counterparts, making the former more sensitive to apoptosis than the latter [102] . In addition to various cells in vitro, γH2A.X detection was also used to quantify the effects of IR in tissues exposed ex vivo or in vivo [109, 110] . With a growing range of applications, γH2A.X analysis expands beyond its traditional field of 4

Oxidative Medicine and Cellular Longevity radiobiology, mainly because of its increasingly recognized role in ROS-related conditions.

Radiotherapy damages living systems and tissues ionizing atoms of the irradiated material resulting in changes in the chemical bonds of the irradiated molecules. By cells absorbing IR, organelles like mitochondria or cellular structures, for example, lipids, proteins, and DNA can be directly damaged [47, 111] . Furthermore, IR can cause persistent alteration of atomic components and macromolecules indirectly through radiolysis of water, thereby changing the endogenous redox system by increasing ROS/RNS such as hydroxyl radicals [112] . Moreover, low-dose IR induces mitochondrial ROS production and metabolic oxidative stress ( Figure 2 ) [113, 114] . Both direct and indirect radiation effects initialize molecular signaling pathways that may repair the damage or culminate in base pair deletion, mutation, or cell death [115] . Comparable to IR, UV radiation also has different modes of disruption, especially UVB [116] . In addition to direct DNA modification via CPD-damage, 6-4-photoproducts, and subsequent collision of the replication fork and DNA strand breaks, UVB rays also have an indirect effect on the DNA via photolysis and generation of hydroxyl radicals (OH·) inducing the formation of 8-hydroxy-2 ′ -deoxyguanosine (8-OHdG), a biomarker of oxidative stress [117] . While UV radiation raises ROS levels both extracellularly and intracellularly [59, 118] , physical plasma influences the cellular redox equilibrium via exclusively exogenously generated ROS, subsequently exerting oxidative stress intracellularly [119] .

Physical plasma is the so-called fourth state of matter after solid, liquid, and gas. By definition, physical plasma is a multicomponent system made of, for instance, electric fields, electrons, ions, thermal and UV radiation, and ROS/RNS ( Figure 3 ). During this phase transition from a gas to the plasma state, electrons are first excited before they dissociate from the atomic shell of the gas molecules. Freely moving electrons and ionized atoms increase the reactivity and electrical conductivity of physical plasmas [7] . With the emission of photons, excited particles return to the ground state, which causes the "plasma glow." The reactive particle mixture contains charged particles, for example, electrons and ions, excited atoms, and molecules [7, 120] . In addition, due to its ionizing effect and interaction with the surrounding air when operated under atmospheric pressure, physical plasma generates ROS/RNS such as O 3 Figure 2 : Effects of ionizing radiation versus ultraviolet radiation versus physical plasma. Absorption of ionizing radiation (IR) affects tissue by directly damaging cellular targets and indirectly through water radiolysis, autoamplifying intranuclear ROS production. Similar to IR, UV, especially UVB radiation, can directly damage the DNA. The indirect action of UVB light is majorly mediated by ROS causing oxidative DNA damage, e.g., 8-hydroxy-2′-deoxyguanosine (8-OHdG). Unlike IR and UVB radiation, ROS/RNS need to travel from the gaseous to the liquid phase and eventually to the cells during plasma treatment. ROS accumulate in the extracellular space and at decreased levels in the intracellular environment after selective transit across the plasma membrane to interact with biomolecules in the cytosol. 5 Oxidative Medicine and Cellular Longevity heavy particles (ions), determine the gas temperature, whereby the plasma temperature correlates with the degree of ionization [7, 125] . In the nonthermal (cold) physical plasma, there is a thermal imbalance in which ions, in contrast to electrons, hardly experience any acceleration (T gas ≙ T Ion < T e− in nonequilibrium plasmas) [7] . With temperatures below 40°C, cold plasma, which is described as partially ionized gas (one particle of 10 9 being ionized), has the greatest degree of tissue compatibility as it is operated at body temperature. The gas composition, gas humidity, and the surrounding environment are further factors influencing the effect of physical plasmas [122, 124, 126] . Cold plasma is usually generated by applying a highfrequency electrical voltage, and the main generation modes are dielectric barrier discharges (DBD) and jet plasmas [127, 128] . The utilization of cold physical plasma in the field of plasma medicine led to the coining of the term 'plasma medicine.' 4.2. ROS/RNS Generation. While plasma acts physically across the spectrum of its emission, the chemical components, especially ROS/RNS, convey the plasma effects in biological systems. Initially, the cold plasma-derived ROS/RNS are generated exogenously in the gas phase [121] . The species then diffuse or penetrate the liquid cell environment, acting on proteins, lipids, nucleic acids, and other biomolecules. Notably, many cold plasma-generated ROS/RNS are similar to those species occurring in physiological processes, such as metabolism and antimicrobial defense. In vitro, where excess liquid dominates over cell-derived biomass, most short-lived plasma-derived ROS/RNS quickly react to more stable species, such as hydrogen peroxide (H 2 O 2 ). Being a nonradical ROS, H 2 O 2 is an integral mediator of intracellular processes of oxidative eustress and distress, leading to signaling and growth stimulation on the one hand and cellular damage and apoptosis on the other [126, 129, 130] . Recently, the types, sources, gradients, and hormetic cellular effects of cold plasma-derived ROS/RNS in cells and tissues have been summarized [119] . Importantly, it has been noted early on that in vitro plasma-induced toxicity follows known processes in cell death research and redox biology [131] . Accordingly, coping with cold plasmainduced oxidative stress follows the concepts laid out by Helmut Sies, being a primary antioxidative protection system acting through enzymatic and nonenzymatic radical scavengers and antioxidants and a secondary system employing repair mechanisms of the DDR machinery [132] . Even if physical plasma is composed of UV radiation, charged particles, and other components, which may support a synergistic cytotoxic effect, extracellular generated ROS/RNS are the mediators of cold plasma cellular efficacy in the current understanding [133] . For the exogenously derived ROS/RNS to become effective, some species can penetrate cells through aquaporins and via diffusion as well Figure 3 : Particle model of the three classical states of matter and active components of the nonclassical fourth state: physical plasma. In the solid state, atoms are held in their position by strong, attractive forces and form a rigid framework. When energy is supplied, the bonds break, the atoms lose their regular order, and the substance liquefies. With a further increase in energy, the atoms lose their cohesion and move freely in space in the gaseous state. Additional energy supply to a gas (ionization) creates gas in an excited state (plasma), a multicomponent system made up of physical and biological-chemical active components. Blue: ions; red: electrons. 6 Oxidative Medicine and Cellular Longevity as cholesterol-dependent lipid peroxidation [134] . Intracellular ROS/RNS influence the cascade of the second messenger calcium (Ca 2+ ) and vice versa [135, 136] . Both ROS/RNS and calcium are involved in apoptosis signaling, and mitochondria and ER are organelles of crucial relevance. ROSinduced oxidative stress after cold plasma treatment leads to mitochondria oxidation, depolarization of the mitochondrial membrane potential Δ Ψ m , and mitochondrial stress [131, 137] . It needs to be emphasized that scavenging exogenous cold plasma-derived ROS/RNS abrogates mitochondrial responses [138] , demonstrating the lack of intracellularly generated ROS/RNS with plasma treatment. Moreover, at the ER, plasma-derived ROS cause an overload of calcium in the cytosol and promote ER stress [139] . Via a distinct region called mitochondria-associated ER membranes, the ER is reversibly bound to mitochondria, and the ER stress results in a calcium influx into mitochondria, eventually decreasing the membrane potential [140] . As a result of the Δ Ψ m collapse, the mitochondria disintegration with the subsequent release of cytochrome c triggers apoptosis induction [141] .

The generation of cold plasma has recently developed into an innovative and attractive research field, and its application is the subject of different industries, especially in biophysics, plasma science, and medicine [142] . Physical plasmas are used to modify biorelevant surfaces, for decontamination purposes, and during argon (hot) plasma coagulation to provide hemostasis via cauterization [143, 144] . Moreover, cold physical plasmas at tissue-tolerable temperatures of around 40°C are used therapeutically and directly on the body surfaces due to their antibacterial, anti-inflammatory, and wound healing properties [145] .

Other promising fields of application are expected in plastic surgery, oral medicine, and ophthalmology [146] [147] [148] .

Oncology is an emerging treatment modality with great potency to convey synergy in the multimodal concept of antitumor therapy [6, 149, 150] . The assumption that cold plasma treatment induces apoptosis in cancer cells is supported by observations of various in vitro and in vivo [151] [152] [153] . However, a recent large-scale study across 35 cancer lines has shown up to 100-fold differences in the sensitivity of tumor cell lines towards cold plasma [154] . ROS of adequate concentration generally mediates a tumor-suppressive effect, which is used in the medical application of cold plasma in particular. Because cold plasma can interact with the tumor microenvironment, the plasma-mediated modulation of immune cells is of specific interest [155, 156] . Already before the recent COVID-19 crisis, several studies had examined the efficacy of cold plasma against viral agents along with plasma devices and design concepts for both sanitation and treatment [157] . A plasma source often used in biomedical research of plasma medicine is the plasma jet kINPen, which is operated at atmospheric pressure and consists of a pin electrode in the center of a dielectric capillary and a grounded outer electrode (Figure 4 ) [158] . Recently, the molecular mechanisms of cold plasmainduced effects were studied more extensively with the kIN-Pen and other cold plasma sources, especially in the light of safety assessment and DNA damage.

A growing body of literature observed a DDR after cold plasma treatment, including recruitment of ATM, H2A.X respectively γH2A.X, and p53. In the light of the pleiotropic roles of γH2A.X, this led to the misleading conclusion that plasma is mutagenic by causing primary DNA damage in the form of DSBs in living cells [14] . Cold plasma-induced γH2A.X was demonstrated cell type-independent in several cold plasma devices (Table 1) [12, 13, [15] [16] [17] [18] [19] [20] [21] [22] [23] [24] [25] [26] [27] [28] . These studies contrast with the results on γH2A.X quantifications in human and porcine skin and oral mucosa ex vivo as well as in vitro genotoxicity and mutagenicity tests according to the OECD (Organization for Economic Co-operation and Development) guideline, none of which had shown any permanent DNA damage after cold plasma exposure [29-31, 33, 34, 159] . So far, only a few investigations in plasma medicine have examined the incidence of cytogenetic damage in cells and tissues using non-γH2A.X assays. However, these observations align with the potentially cytotoxic but neither DNAdamaging nor lasting mutagenic effects of cold plasma [160] . In contrast to UVB radiation, cold plasma-induced γH2A.X did not lead to significantly elevated micronucleus induction, while a correlation between both markers is frequently observed in the field of radiobiology [161, 162] . The lack of a significant increase in the micronucleus frequency as a functional surrogate of genotoxic DSBs is a necessary and sufficient criterion for the hypothesis that cold plasma in plasma medicine has except for-or despite-the H2A.X phosphorylation no sustained genotoxic or mutagenic effect [14, 34] . While this more recent work questioned the unambiguous correlation between γH2A.X and DNA DSBs, the majority of γH2A.X examinations in plasma medicine did not discuss the observation critically that cold plasma-mediated γH2A.X induction does not correlate to DSBs-related MN and do not take into account the interdependence of plasma-generated ROS and phosphorylated H2A.X [87] . Even if the reactive species of intrinsic versus plasma-produced ROS and their cellular targets are fundamentally identical, the theory of plasma-derived ROS directly damaging DNA marked by phosphorylated H2A.X raises doubts at several points along the ROS pathway from extracellular space to the nuclear DNA as explained below ( Figure 4) . Firstly, cold plasma generates ROS/RNS in the gas phase penetrating the liquid cell environment as an additional barrier to the direct plasma-cell-interaction consisting of an antioxidant system. Moreover, the ROS density produced by the plasma source changes with distance from the active plasma zone. Thus, reaching the cell from the outside, the effects of intracellularly occurring and plasmaderived ROS cannot be assumed to be congruent [122, 126] . Secondly, due to their species-specific reactivity, charge, polarity, and short lifetime, only a fraction of the primary extracellular produced ROS can pass through the plasma membrane, either by passive diffusion or by 7 Oxidative Medicine and Cellular Longevity facilitated processes via transporters or channels, for instance, the H 2 O 2 transport through aquaporins [163, 164] . Not only the capacity of the transmembrane transport is limited but also the passage depends on the plasma membrane composition, especially on the cholesterol level [134] . Thirdly, the intracellular milieu offers opportunities for interactions between ROS and numerous reactants and ROS scavengers, including catalase, glutathione peroxidase, and peroxiredoxins, which intercept with the ROS on their 2 to 10 μm long cytoplasmatic diffusion pathway from the cell membrane to the nucleus and decrease ROS level [165, 166] . Only stable ROS/RNS such as H 2 O 2 , nitrite, nitrate, and superoxide can passively diffuse across such distances. Notably, H 2 O 2 is a sturdily nonreactive molecule and reacts with H 2 O 2 -deteriorating enzymes residing at high concentrations in the cytosol 100-1,000 times faster than passive protein oxidation [167] . Fourthly, the remaining ROS must pass through multiple cell organelles and membranes of the ER and ultimately the nucleus. It is unclear how shortlived, reactive species will travel through such protein and lipid-rich environments without finding reaction partners. Fifthly, in the unlikely event such species would make it to the nucleus, there are again antioxidant systems in place in the nucleus to protect against oxidative damage, such as peroxiredoxins 2 (PRDX2) [168] . The argument that H 2 O 2 could make such travels undisturbed to generate hydroxyl radicals in the Fenton reaction is defective due to the cell's lack of free iron pools. Conversely, iron is bound to storage and proteins, such as ferritin [169] . Moreover, if H 2 O 2 and not the short-lived cold plasma-derived ROS/RNS would be responsible for DNA damage, it is not cold plasma that is mutagenic but H 2 O 2 . It should be kept in mind that endogenous H 2 O 2 production during infection control can be exceedingly high, which would lead to the argument that inflammation in wound healing is mutagenic. Altogether, it seems unlikely that short-lived reactive species expelled by cold plasmas are stable and nonreactive enough to travel large distances intracellularly and undisturbed to perform the often-noted DNA-damaging effect.

Considering the limitations of short-lived exogenous species directly traveling to the DNA to perform damage, the question remains why γH2A.X induction is documented by many groups, including ours, following cold plasma treatment in vitro. In short, this is due to DNA damage-independent signaling, as the cell naturally activates its protection systems, including γH2A.X, in response to oxidative stress. Because in radiobiology, ionizing radiation-induced DNA damage and oxidative stress always cooccur, there was neither a need Figure 4 : Obstacles of exogenously (cold plasma-generated) short-lived reactive to species from the extracellular to the nuclear compartment. The plasma jet generates ROS/RNS in the liquid phase around the biological system cell ①. Plasma-liquid interactions and components of the antioxidant system are active in the extracellular space. In addition to diffusion, aquaporins enable the limited ROS/RNS passage, especially H 2 O 2 , across the cell membrane ②. Cholesterol-dependent lipid peroxidation by radicals may facilitate transmembrane diffusion through pore formation. Cold plasma exposure may increase the cytosolic ROS/RNS levels exposing the cell to oxidative stress, which the intracellular antioxidant system, including catalase, glutathione, NADPH+H + , and peroxiredoxins, attempts to counteract ③. Intracellularly, ROS/RNS would have to pass through several structures and membranes of cell organelles, e.g., the ER, to eventually reach the nucleus ④. Finally, intranuclear antioxidant systems also offer protection from oxidative damage ⑤.

Oxidative Medicine and Cellular Longevity nor opportunity to discriminate between in the analysis of H2A.X phosphorylation responses. The differentiation between H2A.X phosphorylation triggered by primary DNA damage and apoptosisassociated H2A.X phosphorylation as well as the kinetics of γH2A.X formation are decisive for the interpretation of the nuclear γH2A.X occurrence concerning its induction mechanisms. Fluorescence microscopy shows intranuclearly an apoptotic ring that includes H2A.X and DDR proteins in apoptotic cells [170] . Moreover, the γH2A.X presence resulting from a highly damaged DNA is divided into two phases: initially, rapid γH2A.X foci are formed; subsequently, apoptosis is initiated, and the γH2A.X-apoptotic ring is formed. Moreover, agents that do not primarily damage DNA and induce apoptosis, such as ligands of the extrinsic apoptosis initiation pathway or intrinsic stress, induce only the second sequence, the apoptotic ring. Theories about DNA damage by ROS are, on the one hand, a site-specific Fenton reaction and, on the other hand, an intracellular increase in calcium concentration, which in turn activates nucleases [171] . Even though γH2A.X is induced through oxidative stress and DNA can be damaged oxidatively, recent conclusions do not ascribe any primarily caused DNA damage in vitro to the plasma treatment [34, 160] . Moreover, even if lipid peroxidation would have a crucial role in facilitating the trans-membrane passage and is a damage mechanism of highgrade oxidative stress, which can contribute to DNA lesions, the oxidative degradation of lipids should not be understood as a critical process of primarily caused DNA damage of exogenous ROS exposure [172] [173] [174] . Comparatively, low ROS concentrations and minor quantities of plasmainduced γH2A.X depending on catalase and pan-caspase inhibition refute lipid peroxidation as a potential mechanism for the DSB formation after exposure to plasmaderived ROS [14, 49] . Moreover, if lipid peroxidation were the DNA-damaging mechanism when applying low-dose ROS, the γH2A.X fluorescence should have increased independently of apoptosis and p38-MAPK signaling pathways, which was not the case in our recent study [14] .

Although proliferating cells intrinsically have more damaged and unwound DNA owing to DNA and protein synthesis, it cannot be concluded that this makes them more susceptible to ROS-induced nuclear damage [72] . Moreover, albeit different studies formulating the idea that overlapping SSBs lead to DSBs and γH2A.X thus appears at the side of the initial DNA damage after such indirect DSB formation, the conclusion that extracellularly released ROS interact directly with the DNA leading to secondary damage seems less likely than the perspective of a ROS-initiated cytosolic signaling cascade, which results in H2A.X phosphorylation Table 1 : Overview of γH2A.X studies in plasma medicine. Both using jet plasmas and dielectric barrier discharge (DBD) as a source of cold physical plasma, γH2A.X was quantified in vitro in low and high malignant cancer cell lines as well as ex vivo in cold plasma-treated tissue. 9 Oxidative Medicine and Cellular Longevity in the nucleus [39, 175] . In addition, the classification of Kalghatgi and colleagues of cold plasma-induced H2A.X phosphorylation being ATR-dependent and ATM-independent is contestable [17] . ATM is a deciphered redox-modulated regulator in the signal cascade upstream of H2A.X phosphorylation. While the kinase is phosphorylated at serine 1981 in response to a DSB, oxidized ATM acts as an active homodimer via covalent intermolecular disulfide bridged to cysteine 2991 , so that ATM has a dual function: it is active towards both DSB and oxidative stress [37, 60] .

The evaluation of the cold plasma effects increasingly focuses on ROS/RNS, which perform their function as cellular signaling molecules or cell-damaging radicals depending on the concentration and localization [85] . Moreover, intracellular changes in the redox system are suggested as a significant event during signal transduction of apoptosis [176] . Equally crucial as directly induced cell death triggered by excessive oxidation of proteins, lipids, or nucleic acids is the potential of ROS to regulate the pathways initiated by other apoptotic stimuli. Particularly, ROS type and source influence the intensity of oxidative stress. It is understood that low ROS levels are agents of redox signaling [177] [178] [179] . Furthermore, the redox-sensitives caspases (cysteine-dependent-aspartate-specific proteases) and the stress-sensitives MAPK-p38 and JNK-are decoded regulators upstream of γH2A.X induction [49, 180, 181] . In agreement with this, pharmacological inhibition of oxidative stress signaling pathways by, e.g., SB202190 (p38-MAPK inhibitor) and the apoptosis inhibition via Z-VAD-FMK (pan-caspase inhibitor) significantly neutralized the ROStriggered but not the UV-induced increase in the γH2A.X levels [14] , indicating a strong dependence of the γH2A.X induction on the p38-MAPK signal and the caspase activation. Accordingly, with regard to the occurrence of phosphorylated H2A.X after cold plasma-derived extracellular ROS/RNS, redox-regulated mediators and mitochondria are presented as intracellular interfaces between ROS and apoptosis signaling pathways [182, 183] . As indicated by Hampton and colleagues two decades ago, intracellular ROS and apoptosis are dependent on caspase activation [184] . Plasma-generated ROS/RNS, especially H 2 O 2 , initiate mitochondria-mediated apoptosis: firstly, by changing the membrane potential and secondly, at the level of mRNA expression through simultaneous up-regulation of H2A.X and proapoptotic genes (Bax) and downregulation of antiapoptotic genes (Bcl-2) leading to caspase activation [12] . It follows that cold plasma triggers the mitochondrial intrinsic apoptosis pathway, which is associated with plasma-induced and redox signaling-associated γH2A.X. Furthermore, redox modulation is ascribed to p38-MAPK, whereby its ROS sensitivity is based apparently on both direct and indirect redox regulation [185] . Direct oxidation of cysteine 162 activates the p38 molecule and influences its interaction with upstream MAP kinases. The indirect regulation, mediated by ROS, occurs via redox activation of upstream kinases such as ASK1 (apoptosis signal-regulating kinase 1) via redoxmediated inactivation of inhibitory MAPK phosphatases [186] . The p38-regulated phosphorylation of H2A.X is also involved in the epigenetic regulation of the expression of proapoptotic Bim during apoptosis induced by the tyrosine kinase inhibitor imatinib chronic myeloid leukemia cells [50] . Accordingly, imatinib stimulates p38, which induces γH2A.X downstream, whose function in connection with apoptosis is closely related to its phosphorylation at serine 139 . This study by Dong and colleagues even reported that γH2A.X expression or the blocking of the p38-MAPKassociated H2A.X phosphorylation by SB202190 sensitizes K562 leukemia cells to apoptosis, which also indicates a central role of γH2A.X in cell death signaling.

Irrespective of DSBs and apoptotic DNA fragmentation, γH2A.X induction was observed in conditions of UVC exposure, which is interpreted as a reaction to JNKmediated phosphorylation of H2A.X [51, 101] . In this constellation, the UVC light-induced phosphorylation represents an early apoptotic process initiated before the CADmediated DNA fragmentation. Analogously to the JNK activation by UVC light, p38-MAPK can be oxidized, stimulating the CAD-mediated nucleosomal DNA fragmentation leading to γH2A.X [180] . Moreover, maximal γH2A.X induction has been shown two hours posttreatment and thus before the apoptosis time window and the beginning of intermediate apoptosis stages, in which γH2A.X increases dramatically in the course of DNA fragmentation [48, 187] . An occurrence of the nuclear γH2A.X without DNA damage and apoptotic fragmentation forces the idea of a phosphorylated histone H2A.X that is strongly intertwined in the signaling of cell death [188] . Recent data with cold plasma even assign γH2A.X a central role in the signaling of the antioxidant defense system [16] . H2A.X knockout cells showed an increase in endogenous ROS levels, could not recruit any element of the antioxidative response via the transcription factor Nrf2 (nuclear factor erythroid 2related factor 2), which is typically activated in the cytosol as a result of redox-active species, and were associated with mitochondrial damage [89, 189] . Cold plasma treatment has been shown to trigger the translocation of the activated cytosolic Nrf2 into the nucleus in vitro and in vivo [190, 191] . Therefore, these results put phosphorylated H2A.X in the light of a secondary event of redox and apoptosis signaling rather than a primary consequence of direct short-lived ROS/RNS-induced DNA damage upon cold plasma exposure.

Medicine. The decades-long hypothesis of a causal relationship that γH2A.X represents a reliable indicator for assessing the DNA damage status and that its presence unambiguously marks DSBs is questioned by more and more studies presenting γH2A.X induction in a more diverse light. Similar to the comet assay as a genotoxic endpoint test, H2A.X phosphorylation does not exclusively indicate DNA lesions but also suggests sensitivity to oxidative stress and apoptosis [192] . In all cases, the phosphorylated H2A.X is a biomarker for DSBs but with clear differentiation in the order in which it occurs. In summary, the cause-effect-consequence relationship of γH2A.X formation is best presented in the following: cold plasma-derived exogenous ROS (cause) mediate intracellular oxidative stress that induced apoptosis (effect) whereby the phosphorylated H2A.X marks the secondary DSBs during CAD-mediated DNA fragmentation (consequence). However, this causal chain does not have unlimited coherence. Based on the observation that untreated cells already express the phosphorylated histone at a basal level, the presence of γH2A.X in cells exposed to low-dose oxidative stressors could be interpreted and discussed as a protective entity of antioxidant defense. Without having a longterm toxic effect on the genome, low ROS concentrations (cause) enable the efficiency of repair mechanisms (consequence), which is supported by γH2A.X (effect) [37] . By contrast, increased agent-induced (cause) intracellular γH2A.X levels (effect) might make a cell more sensitive to apoptosis (consequence), and it could have a suppressive effect on the (malignant) transformation of the cell. The γH2A.X assay appears to be less valid for the specific DSB detection and clarification of molecular mechanisms potentially acting via DNA damage, as the phosphorylated H2A.X represents a DDR biomarker of the first generation. As a biosensor of precancerous lesions, tumor processes, and progression, and as a predictor of antitumor therapy efficacy, phosphorylated H2A.X has great potential in prevention, diagnostic, therapy evaluation, and outcome [82, 105] . It can be assumed that oxidative stress promotes tumorigenesis through ROSmediated proliferation and invasion as well as through endogenous chronic ROS-induced oxidative DNA damage, which could be potentially mapped by increased γH2A.X level as an indicator of genomic instability [193, 194] . However, chronic oxidative stress due to a lack of Nrf2mediated antioxidant response reduces the H2A.X level through protein degradation, which in turn prevents the normal accumulation of γH2A.X after acute stress [195] , making cells more sensitive to cytotoxic and antitumor agents. Yet, this study could not conclude that γH2A.X levels are feasible Figure 5 : Synopsis of the current understanding of the molecular mechanisms of cold physical plasma effects and the γH2A.X induction in the DDR. A plasma jet generates ROS/RNS in the liquid phase around the cell ①. Aquaporins facilitate the limited ROS/RNS passage across the cell membrane ②. Plasma increases the cytosolic ROS concentration and exposes the cell to oxidative stress, which the intracellular antioxidant system senses ③. By activating mitogen-activated protein kinases (MAPK) and increasing the tumor suppressor protein p53, ROS lead to increased expression of the proapoptotic Bax and cold plasma-induced changes in the mitochondrial membrane potential Δ Ψ m initiating the intrinsic apoptosis pathway ④. Plasma-generated ROS also trigger ER stress, which forces mitochondrial disintegration and increased calcium ⑤. In contrast to plasma, UVB light generates ROS intra-and extracellularly. The direct target of UV and ionizing radiation is DNA. While UVB rays induce single-strand breaks (SSBs) ⑥, IR leads to double-strand breaks (DSBs) ⑦. The DNA damage response elements are PI3 kinases; ATR is associated with SSBs, ATM, and DNA-PKcs are associated with DSBs. All three kinases induce the phosphorylation of the nuclear H2A.X to γH2A.X ⑧. In the current understanding, the plasmainduced DDR, including the activation of PI3 kinases and H2A.X, is not a direct plasma effect on the DNA but rather a consequence of plasma-induced redox signaling and apoptosis ⑨.

Oxidative Medicine and Cellular Longevity in risk assessment. Overall, this aligns with another observation showing a clear correlation of γH2A.X and cytotoxicity towards 24 different compounds irrespective of their nature being reportedly mutagenic or nonmutagenic [196] . Consequently, γH2A.X measurements in medical fields and particularly plasma medical research require a careful interpretation of the pleiotropic character of that molecule, including its role in sensing changes in redox homeostasis and apoptotic signaling pathways, are considered and integrated. A mechanistic model is given in Figure 5 . Ultimately, γH2A.X does not represent a valid marker for risk assessment in plasma medicine.

Contrary to treatment with cold plasma, ionizing and UVB radiation-associated γH2A.X is the result of primarily damaged DNA. While the formation of DSB-related micronuclei as genotoxic markers correlates with the nuclear γH2A.X induction for ionizing and UVB radiation but not for cold plasma, plasma but not IR or UVB-light-induced γH2A.X depends on redox-regulated signaling pathways, apoptosis, and caspase activation. IR and UVB act directly on the DNA, after which phosphorylated H2A.X is recruited as part of the DDR, and irreparably damaged DNA promotes apoptosis. However, plasma-derived exogenous and low-dose ROS without sustained genotoxic effects lead to γH2A.X. Consequently, histone H2A.X phosphorylation on serine 139 , initially an indicator of DSBs, does not indicate primarily plasma-induced DNA damage. Physical plasma exerts its biomedical effect through the extracellular release of ROS/ RNS, which diffuse intracellularly to exert oxidative stress and induce apoptosis, rather than directly damaging the DNA. Hence, γH2A.X is not the cause but the consequence of cold plasma-induced apoptosis and possibly a protective mechanism to react to oxidative stress and proapoptotic signaling. Due to its pleiotropic roles apart from the DDR and its interlacing action in redox sensing and signaling pathways of apoptosis, phosphorylated H2A.X is less suitable as a risk marker of DSBs in plasma medicine specifically and putatively other medical fields in general.

The authors declare no conflict of interest.

Histone h2ax phosphorylation: a marker for DNA damage

γH2AX: a sensitive molecular marker of DNA damage and repair

High-content imaging analyses of γH2AX-foci and micronuclei in tk6 cells elucidated genotoxicity of chemicals and their clastogenic/ aneugenic mode of action

Cold atmospheric plasma, a novel promising anti-cancer treatment modality

Targeting malignant melanoma with physical plasmas

Use of coldatmospheric plasma in oncology: a concise systematic review

Plasmas for medicine

The plasma jet kinpen -a powerful tool for wound healing

Clinical experience with cold plasma in the treatment of locally advanced head and neck cancer

Actinic keratoses treated with cold atmospheric plasma

Cold atmospheric plasma (cap) for the treatment of actinic keratosis and skin field cancerization: clinical and high-frequency ultrasound evaluation

Responses of solid tumor cells in dmem to reactive oxygen species generated by non-thermal plasma and chemically induced ros systems

Plasma induced DNA damage: comparison with the effects of ionizing radiation

Elevated H2AX phosphorylation observed with kinpen plasma treatment is not caused by ROS-mediated DNA damage but is the consequence of apoptosis

On cold atmosphericpressure plasma jet induced DNA damage in cells

Cold physical plasma modulates p53 and mitogen-activated protein kinase signaling in keratinocytes

Effects of nonthermal plasma on mammalian cells

Combination therapy of cold atmospheric plasma (CAP) with temozolomide in the treatment of u87MG glioblastoma cells

Non-thermal atmospheric pressure plasma induces apoptosis in oral cavity squamous cell carcinoma: Involvement of DNA-damagetriggering sub-G 1 arrest via the ATM/p53 pathway

DNA damage in oral cancer cells induced by nitrogen atmospheric pressure plasma jets

Cold atmospheric plasma, a new strategy to induce senescence in melanoma cells

Combination of chemotherapy and physical plasma elicits melanoma cell death via upregulation of SLC22A16

Miniature non-thermal plasma induced cell cycle arrest and apoptosis in lung carcinoma cells

Non-thermal plasma induces apoptosis in melanoma cells via production of intracellular reactive oxygen species

DNA damage and mitochondria dysfunction in cell apoptosis induced by nonthermal air plasma

Short and long time effects of low temperature plasma activated media on 3D multicellular tumor spheroids

Low-temperature plasma-induced antiproliferative effects on multi-cellular tumor spheroids

Evaluation of nonthermal plasma-induced anticancer effects on human colon cancer cells

Ex vivo human skin experiments for the evaluation of safety of new cold atmospheric plasma devices

Atmospheric pressure plasma jet application on human oral mucosa modulates tissue regeneration

Porcine intact and wounded skin responses to atmospheric nonthermal plasma

Toxicity and genotoxicity in hela and E. coli cells caused by a helium plasma needle

Risk assessment of a cold argon plasma jet in respect to its mutagenicity

High throughput image cytometry micronucleus assay to investigate the presence or absence of mutagenic effects of cold physical plasma

One year followup risk assessment in SKH-1 mice and wounds treated with an argon plasma jet

Long-term risk assessment for medical application of cold atmospheric pressure plasma

Doxorubicin Activates ATM-dependent Phosphorylation of Multiple Downstream Targets in Part through the Generation of Reactive Oxygen Species

Expression of phosphorylated histone H2AX in cultured cell lines following exposure to x-rays

GammaH2AX foci analysis for monitoring DNA double-strand break repair: strengths, limitations and optimization

Thioredoxins, glutaredoxins, and peroxiredoxins-molecular mechanisms and health significance: from cofactors to antioxidants to redox signaling

Nucleosomal anatomy-where are the histones?

Crystal structure of the nucleosome core particle at 2.8 a resolution

A histone isoprotein with a conserved c-terminal sequence, is encoded by a novel mRNA with both DNA replication type and polya 3'processing signals

Gamma-H2AX in recognition and signaling of DNA double-strand breaks in the context of chromatin

Generation and management of excess histones during the cell cycle

Histone H2A variants H2AX and H2AZ

Atm and DNA-pk function redundantly to phosphorylate H2AX after exposure to ionizing radiation

H2AX phosphorylation after uv irradiation is triggered by DNA repair intermediates and is mediated by the ATR kinase

Regulation of gamma-H2AX and securin contribute to apoptosis by oxaliplatin via a p38 mitogen-activated protein kinase-dependent pathway in human colorectal cancer cells

H2AX phosphorylation regulated by p38 is involved in Bim expression and apoptosis in chronic myelogenous leukemia cells induced by imatinib

H2AX is a target of the jnk signaling pathway that is required for apoptotic DNA fragmentation

PP2A-B56 complex is involved in dephosphorylation of gamma-H2AX in the repair process of CPT-induced DNA double-strand breaks

GammaH2AX foci formation in the absence of DNA damage: mitotic H2AX phosphorylation is mediated by the DNA-PKcs/CHK2 pathway

DNA damage response as a candidate anti-cancer barrier in early human tumorigenesis

DNA: Damage and repair mechanisms in humans

A critical role for histone H2AX in recruitment of repair factors to nuclear foci after DNA damage

Functional interaction of H2AX, NBS1, and p53 in atm-dependent DNA damage responses and tumor suppression

Sensing DNA damage through atrip recognition of rpa-ssdna complexes

Molecular mechanisms of mammalian DNA repair and the DNA damage checkpoints

ATM activation by oxidative stress

Targeting oxidatively induced DNA damage response in cancer: opportunities for novel cancer therapies

GammaH2AX and cancer

Targeting DNA repair and chromatin crosstalk in cancer therapy

DNA double-strand breaks: signaling, repair and the cancer connection

Chromatin modifications and DNA repair: beyond double-strand breaks

Expression of phosphorylated histone H2AX as a surrogate of cell killing by drugs that create DNA double-strand breaks

Atm activation accompanies histone H2AX phosphorylation in A549 cells upon exposure to tobacco smoke

H2AX phosphorylation as a genotoxicity endpoint

Regulation of DNA double-strand break repair pathway choice: a new focus on 53BP1

Low doses of X-rays induce prolonged and atm-independent persistence of γH2AX foci in human gingival mesenchymal stem cells

γ-H2AX as a potential indicator of radiosensitivity in colorectal cancer cells

Histone H2AX phosphorylation after cell irradiation with UV-B: relationship to cell cycle phase and induction of apoptosis

Acidic ph induces topoisomerase II-mediated DNA damage

Heat shock induces phosphorylation of histone H2AX in mammalian cells

A combined gamma-H2AX and 53BP1 approach to determine the DNA damage-repair response to exercise in hypoxia

The contribution of DNA replication stress marked by high-intensity, pan-nuclear gammaH2AX staining to chemosensitization by CHK1 and WEE1 inhibitors

H2AX phosphorylation marks gemcitabine-induced stalled replication forks and their collapse upon S-phase checkpoint abrogation

Initiation of DNA fragmentation during apoptosis induces phosphorylation of H2AX histone at serine 139

Senescing human cells and ageing mice accumulate DNA lesions with unrepairable double-strand breaks

H2ax is required for chromatin remodeling and inactivation of sex chromosomes in male mouse meiosis

Gamma-H2AX: can it be established as a classical cancer prognostic factor?

Gamma-H2AX: a potential biomarker in breast cancer

Genome instability and γH2AX

Histone H2AX phosphorylation is dispensable for the initial recognition of DNA breaks

DNA damage induces reactive oxygen species generation through the H2AX-Nox1/Rac1 pathway

GTPases, genome, actin: a hidden story in DNA damage response and repair mechanisms

Low level phosphorylation of histone H2AX on serine 139 (γH2AX) is not associated with DNA double-strand breaks

Phosphorylation of histone H2AX at M phase in human cells without DNA damage response

miR-24-mediated knockdown of H2AX damages mitochondria and the insulin signaling pathway

Cytometry of atm activation and histone H2AX phosphorylation to estimate extent of DNA damage induced by exogenous agents

DNA double-stranded breaks induce histone H2AX phosphorylation on serine 139

Double-strand break analysis by gamma-H2AX foci: a useful method for determining the overreactors to radiationinduced acute reactions among head-and-neck cancer patients

ATM phosphorylates histone H2AX in response to DNA double-strand breaks

Dynamics of gammaH2AX formation and elimination in mammalian cells after X-irradiation

DNA damage foci: meaning and significance

Endogenous expression of phosphorylated histone H2AX in tumors in relation to DNA double-strand breaks and genomic instability

Radiation sensitivity, H2AX phosphorylation, and kinetics of repair of DNA strand breaks in irradiated cervical cancer cell lines

Telomere-dependent and telomere-independent origins of endogenous DNA damage in tumor cells

Structure and function of histone H2AX

The complexity of phosphorylated H2AX foci formation and DNA repair assembly at DNA double-strand breaks

A minority of foci or pan-nuclear apoptotic staining of gammaH2AX in the S phase after UV damage contain DNA double-strand breaks

Histone H2AX Phosphorylation as a Predictor of Radiosensitivity and Target for Radiotherapy

Uniform widespread nuclear phosphorylation of histone H2AX is an indicator of lethal DNA replication stress

Development of a high-throughput gamma-H2AX assay based on imaging flow cytometry

Gammah2ax in cancer cells: a potential biomarker for cancer diagnostics, prediction and recurrence

Flow cytometric detection of gamma-H2AX to evaluate DNA damage by low dose diagnostic irradiation

Phosphorylation of histone H2AX as a measure of radiosensitivity

Use of the gamma-H2AX assay to investigate DNA repair dynamics following multiple radiation exposures

DNA damage in leukocytes after internal exvivo irradiation of blood with the alpha-emitter Ra-223

Quantitative γ-H2AX immunofluorescence method for DNA double-strand break analysis in testis and liver after intravenous administration of 111InCl3

Ionizing radiation and complex DNA damage: from prediction to detection challenges and biological significance

Potential relationship between the biological effects of low-dose irradiation and mitochondrial ros production

Ionizing radiationinduced metabolic oxidative stress and prolonged cell injury

Oxidative stress: a critical hint in ionizing radiation induced pyroptosis

DNA damage response signaling pathways and targets for radiotherapy sensitization in cancer

Differential effectiveness of solar uvb subcomponents in causing cell death, oncogenic transformation and micronucleus induction in human hybrid cells

Protective effect of topically applied olive oil against photocarcinogenesis following UVB exposure of mice

Measurements of UVgenerated free radicals/reactive oxygen species (ROS) in skin

ROS from physical plasmas: redox chemistry for biomedical therapy

Quantitative detection of plasma-generated radicals in liquids by electron paramagnetic resonance spectroscopy

On the plasma chemistry of a cold atmospheric argon plasma jet with shielding gas device

Non-touching plasma-liquid interaction -where is aqueous nitric oxide generated?

The emerging role of reactive oxygen and nitrogen species in redox biology and some implications for plasma applications to medicine and biology

Numerical analysis of the effect of nitrogen and oxygen admixtures on the chemistry of an argon plasma jet operating at atmospheric pressure

Non-thermal atmospheric pressure discharges

Research on plasma medicine-relevant plasma-liquid interaction: What happened in the past five years?

Dielectric barrier discharges: progress on plasma sources and on the understanding of regimes and single filaments

Atmospheric pressure plasma jets: an overview of devices and new directions

Hydrogen peroxide: a central player in physical plasma-induced oxidative stress in human blood cells

Quantification of the ozone and singlet delta oxygen produced in gas and liquid phases by a non-thermal atmospheric plasma with relevance for medical treatment

Cold physical plasma treatment alters redox balance in human immune cells

Strategies of antioxidant defense

Plasma medicine: a field of applied redox biology

Hampering effect of cholesterol on the permeation of reactive oxygen species through phospholipids bilayer: possible explanation for plasma cancer selectivity

Calcium and ROS: a mutual interplay

Cold atmospheric plasma causes a calcium influx in melanoma cells triggering cap-induced senescence

Effect of vitamin B6 on oxygen radicals, mitochondrial membrane potential, and lipid peroxidation in H 2 O 2 -treated U937 monocytes

Physical plasma elicits immunogenic cancer cell death and mitochondrial singlet oxygen

Nonthermal gas plasma-induced endoplasmic reticulum stress mediates apoptosis in human colon cancer cells

Where the endoplasmic reticulum and the mitochondrion tie the knot: the mitochondriaassociated membrane (MAM)

Atmospheric-pressure plasma jet induces apoptosis involving mitochondria via generation of free radicals

Perspectives on cold atmospheric plasma (CAP) applications in medicine

Plasma surface modification of biodegradable polymers: a review

Medical gas plasma promotes blood coagulation via platelet activation

Plasma medicine: applications of cold atmospheric pressure plasma in dermatology

Plasma in dentistry: brief history and current status

Cold atmospheric pressure plasma jet for the treatment of _Aspergillus_ keratitis

Effects of cold physical plasma on oral lichen planus: an in vitro study (effects of CAP on OLP)

Molecular mechanisms of the efficacy of cold atmospheric pressure plasma (CAP) in cancer treatment

InvivoPen: a novel plasma source forin vivocancer treatment

Cold atmospheric plasma as a novel therapeutic tool for the treatment of brain cancer

Cancer-selective treatment of cancerous and non-cancerous human cervical cell models by a non-thermally operated electrosurgical argon plasma device

Evaluation of the effects of cold atmospheric plasma and plasma-treated liquids in cancer cell cultures

Tumor cell metabolism correlates with resistance to gas plasma treatment: the evaluation of three dogmas

Non-thermal plasmainduced immunogenic cell death in cancer: a topical review

Potentiating anti-tumor immunity with physical plasma

Gas plasma technology-an asset to healthcare during viral pandemics such as the COVID-19 crisis?

The kINPEN-a review on physics and chemistry of the atmospheric pressure plasma jet and its applications

Section 4: health effects

Investigation of toxicity and mutagenicity of cold atmospheric argon plasma

The dose-response relationship for dicentric chromosomes and gamma-H2AX foci in human peripheral blood lymphocytes: influence of temperature during exposure and intraand inter-individual variability of donors

Effect of dose rate on residual gamma-H2AX levels and frequency of micronuclei in x-irradiated mouse lymphocytes

Specific aquaporins facilitate the diffusion of hydrogen peroxide across membranes

Effects of irradiation distance on supply of reactive oxygen species to the bottom of a petri dish filled with liquid by an atmospheric O 2 /He plasma jet

Mitochondrial peroxiredoxin involvement in antioxidant defence and redox signalling

Peroxiredoxins and the regulation of cell death

Estimation of H 2 O 2 gradients across biomembranes

REV7 confers radioresistance of esophagus squamous cell carcinoma by recruiting PRDX2

Iron for proliferation of cell lines and hematopoietic progenitors: nailing down the intracellular functional iron concentration

The nuclear γ-H2AX apoptotic ring: implications for cancers and autoimmune diseases

DNA damage by singlet oxygen and cellular protective mechanisms

ROS-mediated lipid peroxidation and RES-activated signaling

The requirement for iron (III) in the initiation of lipid peroxidation by iron (II) and hydrogen peroxide

In vitro curcumin modulates ferric nitrilotriacetate (Fe-NTA) and hydrogen peroxide (H 2 O 2 )-induced peroxidation of microsomal membrane lipids and DNA damage

Atmospheric pressure plasma jet treatment evokes transient oxidative stress in hacat keratinocytes and influences cell physiology

Oxyradicals and DNA damage

The type and source of reactive oxygen species influences the outcome of oxidative stress in cultured cells

Role of reactive oxygen species (ROS) in apoptosis induction

Overproduction of Nox-derived ROS in aml promotes proliferation and is associated with defective oxidative stress signaling

Cell apoptosis: requirement of H2AX in DNA ladder formation, but not for the activation of caspase-3

Impact of non-thermal plasma treatment on MAPK signaling pathways of human immune cell lines

Mitochondrial regulation of cell cycle and proliferation

Cysteine-mediated redox signalling in the mitochondria

Redox regulation of the caspases during Apoptosisa

Redox regulation of protein kinases

Atmospheric gas plasma-induced ros production activates TNF-ASK1 pathway for the induction of melanoma cancer cell apoptosis

Apoptosis time window induced by cold atmospheric plasma: comparison with ionizing radiation

Cold atmospheric plasma treatment induces anti-proliferative effects in prostate cancer cells by redox and apoptotic signaling pathways

Histone H2AX deficiency causes neurobehavioral deficits and impaired redox homeostasis

Non-thermal plasma activates human keratinocytes by stimulation of antioxidant and phase II pathways

Nrf2 signaling and inflammation are key events in physical plasma-spurred wound healing

Comet assay and early apoptosis

Cancer, oxidative stress, and metastasis

Role of oxidatively induced DNA lesions in human pathogenesis

Chronic oxidative stress promotes H2AX protein degradation and enhances chemosensitivity in breast cancer patients

The γH2AX assay for genotoxic and nongenotoxic agents: comparison of H2AX phosphorylation with cell death response

This study was funded by the German Federal Ministry of Education and Research (Bundesministerium für Bildung und Forschung (BMBF), grant number 03Z22DN11) and the Gerhard-Domagk-Foundation Greifswald, Germany.