key: cord-0033418-mrh2pbi6
authors: Dumitrascu, Georgiana R.; Bucur, Octavian
title: Critical physiological and pathological functions of Forkhead Box O tumor suppressors
date: 2013-12-31
journal: nan
DOI: 10.15190/d.2013.5
sha: 6dccfa342b218c6dbe68ead6131d72369aa6e467
doc_id: 33418
cord_uid: mrh2pbi6

The Forkhead box, subclass O (FOXO) proteins are critical transcription factors, ubiquitously expressed in the human body. These proteins are characterized by a remarkable functional diversity, being involved in cell cycle arrest, apoptosis, oxidative detoxification, DNA damage repair, stem cell maintenance, cell differentiation, cell metabolism, angiogenesis, cardiac development, aging and others. In addition, FOXO have critical implications in both normal and cancer stem cell biology. New strategies to modulate FOXO expression and activity may now be developed since the discovery of novel FOXO regulators and non-coding RNAs (such as microRNAs) targeting FOXO transcription factors. This review focuses on physiological and pathological functions of FOXO proteins and on their action as fine regulators of cell fate and context-dependent cell decisions. A better understanding of the structure and critical functions of FOXO transcription factors and tumor suppressors may contribute to the development of novel therapies for cancer and other diseases.

The Forkhead box (FOX) proteins represent a wide family of transcription factors that display an extraordinary functional diversity, regulating a variety of critical biological processes 1, 2 . FOX proteins are well known to control the following physiological procceses: apoptosis, cell-cycle, cellular metabolism, immune response, differentiation, development (such as cardiac development) or aging. FOX proteins are also involved in various pathologies, such as cancer, diabetes and neurodegenerative diseases 3, 4 .

The first forkhead transcription factor was first identified in 1989, and its function was related to the development of the anterior and posterior gut of the Drosophila embryo. The "forkhead" name was given because of the two spiked-head structures found in the embryos of the Drosophila Melanogaster forkhead mutant presenting modifications of the gut formation 5 . One year later, the sequence comparison between forkhead and mammalian hepatocyte-enriched transcription factor HNF-3A showed a conserved 110-aminoacid DNA binding domain, bringing evidence that forkhead proteins are a new class of transcription factors 6 .

Hence, forkhead transcription factors are defined by their winged-helix DNA binding domain, a conserved structure called "Forkhead box", the symbol FOX being assigned to all vertebrate forkhead transcription factors, according to the revised nomenclature 7 .

Since its discovery, numerous forkhead genes have been identified in a broad range of organisms, from yeast and worms to humans 2 . Interestingly, up to now, FOX genes have not been identified in plants 8 . However, an update published in 2010 reported that are 50 FOX genes identified and classified in the human genome and 44 in the mouse genome 9 . Therefore, a standard nomenclature system was required for this extended number of discovered factors. In 2000, Daniel E. Martinez and his team established Fox Nomenclature Committee, the first step towards an unified nomenclature for the winged-helix / forkhead transcription factors. The Committee has changed the initial terms for the forkhead proteins (e.g. FREAC -Forkhead RElated Activator; fkh -Drosophila gene fork head) 7 . Currently, based on phylogenetic analysis, FOXO genes are classified in subclasses that range from FOXA to FOXS to yield 23 subclasses in total 10, 11, 12, 13 . Each subclass has several members noted with an arabic number. While for human forkhead proteins abbreviations have all letters in uppercase (e.g., FOXD3), for mouse only the first letter is capitalized (e.g., Foxd3) and for all other chordates the first and subclass letter are in uppercase (e.g., FoxD3) 7 .

One of the largest and the most important subclass of FOX family is represented by FOXO (Forkhead box, subclass O) transcription factors. FOXO transcription factors (FOXOs) are characterized by the same conserved DNA binding domain that define the family of forkhead proteins 1 . However, FOXOs share an additional unique 5 amino acid sequence insertion within the DNA binding domain that is not present in other forkhead proteins 14 .

Only one FOXO transcription factor is known in invertebrates (named abnormal dauer formation protein 16/DAF-16 in the nematode worm Caenorhabditis elegans and dFOXO in the fruit fly Drosophila melanogaster), while in mammals four FOXO proteins encoded by four different genes were identified: FOXO1, FOXO3, FOXO4 and FOXO6 15 .

Initially, FOXO1 transcription factor (previously known as FKHR-forkhead in rhabdomyosarcoma) was identified through its involvement in chromosomal translocations t(2;13) and t(1;13) in alveolar rhabdomyosarcoma tumors due to PAX3/7-FKHR fusion transcript 16, 17 . A few years later, FOXO3 (previously known as FKHRL1 -forkhead in rhabdomyosarcoma like protein 1) was characterized and named, based on similarities to FKHR 18 . The gene for FOXO4 was described as being fused to MLL transcription factor as a result of the t(X; 11) chromosomal translocation in acute lymphoblastic leukemia, therefore, the initial term for FOXO4 was AFX (The acute leukemia fusion gene located on chromosome X) 19 .

FOXO proteins are considered unique cellular targets, regulating a wide variety of critical cellular processes, such as: apoptosis, oxidative stress, DNA damage repair, cell cycle, stem cell proliferation and maintenance, metabolism, angiogenesis, vascular tone, cardiovascular development, fertility, immune response and neuronal survival 4, 20 . The aim of this review is to discuss the most recent advances in elucidating the functions, structure and transcriptional regulation of Forkhead Box O transcription factors, both in physiological and pathological conditions. The advances in understating the mechanism of FOXOs regulation of stem cells, cancer stem cells and how non-coding RNAs are regulated and regulate the function of FOXO genes/protein are presented.

In humans, the primary structure of the FOXO proteins is characterized by a length of approximately 655-675 amino acid residues (aa) for FOXO1 (655 aa) and FOXO3 (673 aa), and a shorter sequence of approximately 500 amino acids for FOXO4 (505 aa) and FOXO6 (492 aa) 21,22,23,24 . All members of the FOXO family consist of four domains: a forkhead DNA-binding domain (DBD), a nuclear localization signal (NLS), a nuclear export sequence (NES) and a C-terminal transactivation domain 25 (Figure 1) .

The forkhead DNA-binding domain (DBD), also called the forkhead box, is described as a "winged helix" due to the butterfly-like aspect on X-ray crystallography and nuclear magnetic resonance 26 . Analysis of the amino acid sequences alignment of FOXO proteins revealed a highly conserved DNA binding domain among all the members of the broader group of forkhead transcription factors, but also among species, in eukaryotic organisms, from yeast to humans 3, 27 . Moreover, several studies point out that forkhead DBD is not the only region in the FOXO molecule that is highly conserved. Similarities were also observed in the N-terminal region near the first AKT/protein kinase B (PKB) phosphorylation site (Thr24 for FOXO1 and Thr32 for FOXO3), the region containing NLS, and sequences from C-terminal transactivation domain 25 . As mentioned above, the forkhead domains in FOXO subclass of FOX family are similar to the forkhead regions of other subclasses. For example, structural similarities have been proven in the core region of FOXO3 compared to FOXA3, FOXK1 and FOXP2 28 . The forkhead/winged helix motif is a shared sequence between subclasses of FOXO, of around 100 amino acids that folds into three alphahelices (H1, H2 and H3), three beta-strands (S1, S2 and S3) and two wing-like loops (W1 and W2). The structure has a H1 -S1 -H2 -H3 -S2 -W1 -S3 -W2 topology and the strands S1, S2 and S3 interact with each other forming a beta-sheet. While the N-terminal part of the domain is formed by a cluster of three alpha-helices, the C-terminal half consists of beta strands S2 and S3 and two large loops (wings W1 and W2) 25 . The main DNA recognition site is represented by the highly conserved helix H3 of forkhead DNA-binding domain. The stability of forkhead DBD -DNA complexes is increased by the more variable regions of the DBD, including H1, the region between H2 and H3, wing W1 and C-terminal segment 25 .

Although the FOXO forkhead box is clearly related to those found in other forkhead genes, all FOXO members contain an aditionally segment of five amino acid (198-GDSNS-202) between helices H2 and H3, that creates a small extra loop, forming a coil structure in the FOXO3 DBD, and a short helix in the FOXO4 DBD 28, 29 . This is important in sequence-specific interactions with DNA-binding sites 30 .

FOXO proteins mediate transcriptional activation through binding to the conserved consensus core motif TTGTTTAC in the DNA 31 . They bind DNA through a FOXO-recognized element with a T/C-G/A-A-A-A-C-A-A consensus sequence in the forkhead DBD (C-terminal) 26 . There are fourteen protein-DNA contacts described, which mediate the activation/inhibition of FOXO's target genes, such as Bim, TRAIL, p27, p21 and catalase. The main recognition site is the α-helix H3 32 .

Forkhead proteins function as transcription factors that bind to DNA through their forkhead domain in order to upregulate or downregulate the expression of a tremendous number of target genes 20 . Hence, the FOXO transcription factors control the expression of a wide spectrum of genes that regulate essential physiological cellular processes, such as cell death/cell survival, cell cycle, cell proliferation, cell differentiation/development, angiogenesis, cell metabolism, stress response and stem cell maintenance 33,34,35,36,37,38 (Figure 2) . Moreover, FOXOs are also involved in a wide range of pathological cellular processes, such as cancer, neurodegenerative diseases (Parkinson's disease, Alzheimer), diabetus mellitus, cardiac failure, atherosclerosis, hypertension and anovulation 39, 40, 41, 42, 43, 44, 45, 46 .

Differences between functions and regulatory mechanisms of FOXO1 and FOXO3 proteins are considered to be partially redundant, with several exceptions. For example, AKT phosphorylates all FOXO family members, inducing their translocation into the cytoplasm and inactivation, while PP2A dephosphorylates part of the AKT phosphorylation sites in FOXO1 and FOXO3, reactivating them 47 . Several particular differences regarding the regulatory kinases, E3 ligases or other important enzymes and regulators exist. Thus, their activity is in part controlled by different mechanisms 31 .

FOXO transcription factors regulate the expression of multiple pro-apoptotic and anti-apoptotic proteins, and they have the ability to induce apoptosis by activating either intrinsic or extrinsic pathways of apoptosis 48,49,50,51,52 . Moreover, the consensus FOXO recognition element (FRE) -(G/C)(T/A)AA(C/T)AA -which differs from that of other forkhead proteins, seems to have a very important role in both apoptotic pathways, since matching functional FRE sites have been identified in the promoters of FOXO target genes encoding Fas ligand (FasL), insulin like growth factorbinding protein 1 (IGFBP1), the apoptotic regulator Bcl-2 interacting mediator of cell death (Bim) and others 30 .

FOXO triggers the mitochondria-dependent intrinsec apoptotic pathway through upregulation of multiple pro-apoptotic Bcl-2 family members, such as Puma, Bim, NOXA, BNIP3, and downregulation of the anti-apoptotic Bcl-2 family member Bcl-xL 48,49,50,51,52 . The expression of the anti-apoptotic protein Bcl-xL is suppressed by FOXO proteins, such as FOXO4, after increasing the expression of the transcriptional repressor Bcl-6, in order to trigger apoptosis 52 .

Both FOXO-induced expression of the proapoptotic Bcl-2 family members and FOXOdownmodulated anti-apoptotic Bcl-2 family members lead to apoptosis due to mitochondrial outer membrane permeabilization (MOMP), as a response to intracellular stress, growth factor deprivation or other factors 53 . These mitochondrial modifications result in release of cytochrome c, Smac/DIABLO and Omi/HtrA2 from mitochondria, subsequently triggerring downstream caspases activation 54,55 . Apaf 1 binds cytochrome c forming a complex named Apoptosome, required for caspase 9 activation (initiator caspase) 54 . Caspase 9 activation further activates the effector caspases, such 3, 6 or 7, triggering caspase cascade 54 .

FOXO proteins are also able to induce apoptosis by activating the receptor-dependent extrinsic pathway of apoptosis. They induce the upregulation of the death receptor ligands FasL and TRAIL, promoting an autocrine and/or paracrine action of these death ligands on the death receptors 56 . Fas signaling pathway is important in apoptosis induction through the extrinsic pathway, since Jurkat cells lacking several critical components of Fas pathway fail to induce FOXOdependent cell death 57 . Upregulation of tumor necrosis factor related apoptosis inducing ligand (TRAIL) by increased levels of FOXO1 or FOXO3 in cancer cells, such as prostate carcinoma cells, leads to apoptosis 58 . Thus, binding of Fas ligand (FasL) and TRAIL to their receptors (Fas/CD95/APO-1 for FasL and DR4, DR5 for TRAIL) triggers a death-inducing signaling complex (DISC) with a subsequent activation of caspases, mainly initiator caspase 8 and effector caspase 3, leading to apoptosis 59 . Moreover, FOXO transcription factors directly regulate the expression of tumor necrosis factor receptorassociated death domain (TRADD). Activation of FOXO proteins by PI3K-AKT pathway inhibitors results in increased expression of TRADD protein 60 . TRADD is an important adaptor protein interacting with TNFR1 and Fas receptors, mediating apoptosis and NFkB pathway activation 61 .

Under normal physiological conditions, cyclins and their associate cyclin dependent kinases (CDKs) are very important for the progression of the cell cycle 62 . In response to DNA damage, FOXO transcription factors increase the expression levels of the CDK inhibitors binding to cyclin/CDK complexes, such as p21 (also known as CDK inhibitor 1) and p27 (Kip1) 63,64 . CDK inhibitors together with FOXO-induced inhibition of Cyclins expression act by stopping the cell cycle at different checkpoints in order to repair the DNA damage or to remove the damaged cell 65 . For example, a study performed on 32D murine myeloid cells and on BaF3 murine pre-B-cell lines brings evidence that endogenous FOXO proteins are required to enforce cell cycle checkpoints after The cell cycle arrest at G1/S transition is induced by FOXO by upregulating the negative regulators of the G1/S phase, such as the CDK inhibitors: p27 KIP1 , p57 KIP2 , p21 CIP1/WAF1 (CIP/KIP family), p15 INK , p19 INK (INK family) and the retinoblastoma protein family member p130 27 .Also, FOXO decreases the positive regulators, such as cyclin D1, or cyclin D2, blocking the G1/S transition 66 . Additionally, FOXO increases the expression of negative regulators such as Gadd45alpha and cyclin G2, resulting in cell cycle arrest at G2/M 66 . Surprisingly, FOXO proteins act as transcription factors for PLK1 expression during cell cycle, PLK1 being critical in promoting G2-M phase transition, M phase progression and end of mitosis 67 . A complete knock-down of FOXO protein levels induces an arrest in cell cycle, suggesting that a basal, low levels of FOXOs activity is required for the cell cycle progression 67 . Surprisingly, in specific settings, FOXO may actually serve as a promoter of proliferation. For example, neutrophils isolated from FOXO3 deficient mice show high levels of FasL expression and apoptosis, revealing that FOXO3 may represses FasL expression in neutrophils, leading to proliferation in this type of cells 68 . FOXO1 was also shown to positively influence proliferation induction in pancreatic β cells in vitro, under low nutritional circumstances. The mechanisms implicated in this process are not completely understood. However, the induction of Ccnd1 gene transcription, which encodes Cyclin D1, may at least partially be involved. Cyclin D1 represents one of the earliest cell cycle-related events, being critical for the G1 to S phase progression during the cell cycle 34 .

Thus, FOXO proteins coordinate the expression of multiple important cell cycle regulators, in order to block the G0/G1, G1/S or the G2/M transitions during cell cycle when needed, such as after DNA damage. However, a basal level of FOXO proteins is required for G2-M cell cycle transition, when FOXO-dependent PLK1 expression seems to be necessary. These results suggest that FOXO proteins have to be tightly regulated and are important and sensitive regulators of cell cycle, proliferation and other critical cellular processes.

FOXO proteins play an important role in regulating differentiation of a wide variety of tissues. It is well known that FOXOs can control the differentiation of precursor cells into muscle, adipose tissue or blood cells. Interestingly, FOXOs effect on differentiation is context dependent and sometimes FOXO isoform dependent. While FOXO3 promotes differentiation of erythroid cells, FOXO1 suppresses the differentiation of precursor cells in adipose and muscle tissues 69 . FOXOs can also suppress bone formation by inhibiting Wnt-β catenin-TCF signaling. Wnt signaling is known to stimulate bone formation 70 .

Moreover, FOXO proteins are required for maintenance of somatic/adult stem cells, such as hematopoietic stem cells, and they also regulate cancer stem cells 71 (see details in Chapter 5).

Metabolic signaling mediated by forkhead transcription factors is conserved among multiple species, including but no limited to mammals, Drosophila melanogaster and Caenorhabditis elegans 20 . It was first noticed for the FOXO homolog named Dauer Formation-16 (DAF-16), in the Caenorhabditis elegans worm 72 .

FOXO proteins are involved in critical physiological processes that regulate cellular metabolic activity in many organs, such as liver, pancreas, adipose tissue and hypothalamus 73, 74, 75, 76 . In the liver, FOXO1 forms a complex with another transcription factor, the liver specific PGC1alpha, in order to induce gluconeogenesis by upregulating G6Pase and PEPCK genes. This is important for maintaining glucose homeostasis 73 . Confirming these results, loss of hepatic FOXO genes in mice induces a downmodulation of gluconeogenesis and an upregulation of glycolysis 77 . In addition, ectopic expression of FOXO1 in rat primary hepatocytes increases apocIII, an inhibitor of lipoprotein lipase, suggesting that FOXO1 is involved in regulating the lipid metabolism 78 . Recently, nicotinamide phosphoribosyltransferase (Nampt) gene was described to be a new transcriptional target gene of FOXOs for regulating hepatic triglyceride levels 79 . In pancreas, FOXO1 plays an important role in the maintenance of beta cell function, but also in the development of the pancreas, through repression of the pancreatic transcription factor Pdx1 74 . Aditionally, FOXO1 increases the food intake by upregulating AgRP and NpY, and by downregulating POMC in hypothalamus, antagonizing the anorexigenic hormone leptin 76, 80 . Recently, G-protein-coupled receptor Gpr17 was described to be a FOXO1 target that activates AgRP, suggesting a new mechanism for FOXO1-AgRP mediated food intake that might provide a new treatment for obesity 81 .

All these results establish FOXO proteins as important regulators of cellular metabolism and potential target in metabolic related diseases.

FOXO transcription factors function as sensors for reactive oxygen species (ROS) and play an important role in cellular resistance to stress, increasing cellular survival. FOXO proteins are able to protect the cell from oxidative damage, decreasing the availability of ROS. They stimulate the expression of certain genes responsible for the ROS inactivation, such as the antioxidant enzymes manganese superoxide dismutase (MnSOD), that catalyzes the conversion of superoxide to hydrogen peroxide, and catalase, that converts hydrogen peroxide into water and oxygen 27 . Studies on human cardiac fibroblasts revealed that FOXO also modulate the antioxidant enzyme peroxiredoxin III, fighting against cell damage induced by oxidative stress. Concomitant peroxiredoxin III knockdown and FOXO3 knockdown resulted in higher levels of hydrogen peroxide in response to serum starvation, as compared to peroxiredoxin III knockdown only 82 . Other FOXO transcriptional targets (Figure 3 ), such as sterrole carrier proteins (SCPs), are now known to play an important role during the defence against oxidative stress. SCPs are implicated in protecting fatty acids from peroxidation 83 . FOXO proteins are also able to increase DNA repair, inducing a cell cylce arrest at G2/M checkpoint, in order to provide time for repairing the DNA damage. One of the transcriptional target of FOXO, implicated not only in cell cycle arrest but also in DNA repair and cell survival in response to cellular stress, is Gadd45 84 . Similarly, DDB1 gene protein product is able to repair the DNA damage through upregulation by FOXO 69 .

FOXOs regulate the longevity of the cell mainly by increasing resistance to stress, modulating the DNA repair process and maintaining the stem cells 27 . The lifespan extension is an important function of FOXO that is conserved among several species. A well studied example is the role of FOXO homologous DAF-16 (Caenorhabditis elegans) in aging 85 . Loss of FOXO3 in human skin fibroblasts results in aging specific morphological changes, suggesting that FOXO3 is necessary for maintenance or promotion of cellular longevity 86 . Moreover, loss of FOXO3 activity leads to decreased MnSOD and enhanced cell injury in vascular smooth muscle explanted from aged mice, due to limied ROS inactivation 87 . Thus, cellular lifespan maintenance requires a certain level of FOXOs activity and this is mainly achieved by inactivation of AKT activity 88 . FOXO proteins do not only play an important protective role during senescence/aging, but also during exercise. It was previously suggested that FOXOs may at least partially be involved in the exerciseinduced beneficial cardiac effects. Interestingly, exercise induces an upregulation of FOXO3 and SIRT1 in the heart, with subsequent increased MnSOD, catalase and GAD45alpha, and decreased Cyclin D2, suggesting the protective role of FOXO proteins 89 .

Interestingly, other studies revealed that, in conditions of oxidative stress, FOXO3 is also able to induce apoptosis by triggering a Fas-mediated death pathway in cultured motoneurons, by activating TRAIL, BH3-only proteins Noxa and Bim, and by promoting pro-apoptotic activity of p53 20 . Additional reports suggest that suppression of FOXO proteins expression during oxidative stress can be protective to some extent for cells, since protein inhibition or gene knockdown of FOXO1 and FOXO3 decreases the ischemic infarct size in the brain, protects the metabotropic glutamate receptors during vascular injury, enhances pancreatic β-cell or neuronal survival through NAD + precursors and provide trophic factor protection with erythropoietin (EPO) and neurotrophins 20 . This suggests that while a certain level of FOXO3 activation is required in cellular stress resistance, sustained activation or activation over a threshold of FOXO3 is detrimental and may induce apoptosis. Thus, FOXO3 plays an important role in cellular decision during stress, helping the cells to survive by multiple mechanisms (such as DNA repair, ROS inactivation etc) and inducing apoptosis when DNA or cellular damage can't be repaired. 

FOXO proteins play a central role in maintaining the immune response of the human body. Cell type-specific deletions of FOXO1 and/or FOXO3 in mice revealed an important role of FOXO proteins in regulating immunological homeostasis and tolerance, by controlling the function and development of B and T lymphocytes. Thus, FOXO1 and FOXO3 are essential transcription factors involved in early B cell development and peripheral B cell function, since early deletion of FOXO1 blocked B cell differentiation at the pro-B cell stage. This is due to a defect in interleukin 7 receptor alpha (IL-7Ralpha) expression. Deletion of FOXO1 in peripheral B cells was associated with defective expression of both CD62L and AID, with subsequent failure in class-switch recombination and reduced IgG production upon immunization. Moreover, it is known that the PI3K-AKT-mediated inactivation of FOXO1 is essential for the optimal proliferation of B cells, while ectopic expression of PI3K-independent variants of FOXO1 or FOXO3 (active triple mutants at the AKT phosphorylation sites) resulted in cell cycle arrest and increased cell death in B cells 90 . Another study on mice with T cell-specific deletion of FOXO1 showed a decreased expression of IL-7 receptor on mature T-cells, suggesting that IL7-R is a transcriptional target of FOXO1, which is mediating through binding with IL-7 the survival and homeostatic proliferation of peripheral T cell 91 .

Excesive inflammatory cells may become harmful for the human body through the generation of ROS and through the production of cytokines. Studies performed on mice deficient of FOXO3 ilustrated lymphoproliferation, inflammation of the salivary glands, lung, and kidney, and increased activity of helper T cells. These observations demonstrate the beneficial role of FOXO proteins in human body, by preventing T cell hyperactivity 20 . Also, it was demonstrated that miR-182 has a central role in the late phase of clonal expansion of the helper T lymphocytes, by inducing IL-2 which is able to inactivate FOXO1. FOXO1 was found to be a suppressor of proliferation in resting helper T lymphocytes and, in order to allow proliferation, T cell activation via TCR/CD28 and IL-2R signaling must inhibit FOXO1 90 . Other studies reported that T cells derived from Bim and Puma deficient mice were resistant to apoptosis after IL-2 deprivation, demonstrating that FOXO3, through upregulation of Bim, Puma and p27 Kip1 is important for the induction of cell cycle arrest and apoptosis of T cells, in the absence of cytokines 48 . FOXO proteins may be benefical for autoimmune disorders by inducing a Fas mediated apoptosis that target activated T cells, followed by a decrease in cytokine stimulation in patients with autoimmune lymphoproliferative syndromes 20 .

FOXO proteins play an important role not only during physiological cellular processes, but also in few pathologies, such as cancer. FOXOs are well known tumor suppressor proteins.

Although FOXO proteins protect the human body by playing a central role in a wide range of mainly physiological functions (as described earlier), under some circumstances, FOXO's roles can become harmful for the human cells. This is because FOXO is also involved in a number of pathological functions, such as inflammation and muscle atrophy. For example, apoptosis places FOXO proteins on the good side when it leads to tumor suppression. However, cellular apoptosis can become itself a significant component for pathology in diseases such as neurodegenerative disease, diabetes mellitus (DM), and cardiovascular injury 40,41,92,93 .

Cancer: FOXO proteins are tumor suppressors FOXO proteins are inactivated in a wide variety of malignancies, eiher posttranslational (mainly by PI3K-AKT mediated phosphorlation) or by fusion mutations (such as PAX3-FOXO1; MLL-FOXO3, MLL-FOXO4) 94, 95 . Inactivation of FOXO by PI3K-AKT pathway activation is a common feature of many malignancies, such as prostate cancer, breast cancer, leukemia and glioblastoma 69 . Conditional deletion of FOXO family members in mice leads to the lymphomas and hemangiomas, which suggests that loss of FOXOs maintains or promotes survival of tumor cells 96 . FOXOs loss or inactivation is known to play an important role in cancer tumorigenesis or progression, in vivo 97 . For example, a recent study described a significant correlation between low expression of FOXO3 and a poor prognosis for gastric cancer patients, bringing evidence that FOXO3 could be a valuable prognostic biomarker for patients with gastric cancer 98 . In addition, FOXO3 overexpression was shown to reduce motility, invasiveness, and aggressiveness in estrogen receptor α-positive (ERα+) breast cancer cells 39 .

FOXO proteins exert their tumor suppressor functions predominantly by promoting cell cycle arrest, apoptosis, ROS inactivation and DNA repair, through expression of their target genes 47,99 . For instance, FOXO3-induced expression of Bim, a pro-apoptotic member of the Bcl-2 family of proteins induced a caspase-dependent cell death in several types of cancers, such as in chronic leukemias, breast and gastric cancers 27 . Similarly, FOXO-induced TRAIL and NOXA expression induces apoptosis in many malignancies, including leukemias 100 .

Interestingly, FOXO3 can also inhibit the protooncogene c-myc, indirectly controlling the transcription of a wide set of target genes implicated in cell survival, cell cycle, apoptosis and tumorigenesis. Myc is a transcription factor and a well known promoter of survival, proliferation and tumorigenesis, being found upregulated in a large variety of malignancies. Noteworthy, activation of FOXO proteins not only induces cell cycle arrest or apoptosis, but also a differentiation program. In chronic myeloid leukemia (CML), FOXO3 can induce CML leukemic cells differentiation, by inhibiting the expression of Id1 (Inhibitor of DNA binding 1). CML is characterized by the presence of the Bcr-Abl fusion protein, which is a constitutive active kinase, controlling many crucial downstream pathways implicated in cell cycle, proliferation, apoptosis and cell adhesion. Bcr-Abl activates PI3K-AKT pathway, inactivating FOXO proteins and their pro-apopotic and cell cycle arrest signals 27 . The use of the Tyrosine Kinase Inhibitors (TKIs) and of the proteasome inhibitor Bortezomib results in inhibition of Bcr-Abl activity and its downstream pathways, with a subsequent activation of FOXO proteins 102 .

TKIs treatment induces a FOXO-dependent suppression of Id1 expression, leading to K562 Bcr-Abl positive cell line differentiation. Thus, Bcr-Abl can maintain the leukemic state not only by promoting proliferation, cell cycle progression and inhibiting apoptosis, but by also inhibiting FOXO-mediated differentiation 27 .

Inflammation (rheumatoid arthritis, osteoarthritis, systemic lupus erythematosus) It was shown that loss of functional FOXO proteins lead to inflammatory cell activation in several disorders, with the subsequent cellular damage, through oxidative stress and excess of cytokines. Inactivation of FOXO3 in T lymphocytes, as well as inactivation of FOXO1 and FOXO4 in synovial macrophages in patients with rheumatoid arthritis and osteoarthritis result in inflammatory cell activation. In addition, loss of FOXO proteins may be a potential etiology for systemic lupus erythematosus (SLE) and rheumatoid arthritis, since FOXO1 gene transcript levels are downregulated in peripheral blood mononuclear cells of these patients 20 . A link between inflammation, insulin resistance and FOXO transcription factors was previously suggested when downregulated FOXO1 decreased the levels of C/EBP beta transcription factor in adipocytes, with the subsequent reduction in expression of the pro-inflammatory cytokines CCL2 (chemokine ligand 2) and IL-6 103 . Thus, FOXO1 indirectly might induce an inflammatory status of the adipose tissue, responsible for the insulin resistance in type 2 diabetes. Yet, there are studies that describe the ability of FOXO proteins to directly induce inflammation through upregulation of the inflammatory cytokine IL-1b 104 . However, further experiments are required in order to clearly understand the context related mechanisms of FOXO-dependent modulation of inflammation.

Muscle atrophy appears in a variety of diseases, including cancer, diabetes and sepsis, and is characterized by accelerated proteolysis that can be induced through two pathways: the ubiquitinproteasome pathway and through lysosomal pathway, as a consequence of autophagy 27 . Studies revealed that FOXO proteins can induce muscle atrophy, characterized by decreased muscle function 105 . Thus, FOXO proteins have been shown to increase the transcription of key regulators of both lysosomal and proteasomal proteolysis: the autophagy followed by the lysosomal proteolysis is stimulated by upregulation of Bnip3, LC3, and Gabarapl1, while the proteasomal proteolysis is induced by increasing the ubiquitin ligase atrogin1. It was also shown that FOXO3 activity is both required and sufficient for induction of autophagy in muscle cells, since studies performed on adult muscle fibers from mice show that the ectopic expression of an active FOXO3 mutant leads to lysosomal proteolysis after formation of autophagosomes, while the knockdown of FOXO3 in these muscles fibers blocked autophagosome formation after starvation 106, 107 .

Autophagy has a critical role in maintaining the cellular and metabolic homeostasis. It seems that the metabolic status of the cell strongly influences this process in both normal cells and cancer cells, despite the profound differences in their metabolism 108 . In cancer cells, ATP is predominantly produced through the constitutive activation of aerobic glycolysis, process that is modulated by the transcription factor HIF1α 108 . Since p38α is required to maintain the levels of HIF1α target genes, researchers demonstrated that in colorectal cancer cells, the inhibition of p38α causes a rapid drop in ATP levels, with an acute energy need which activates FOXO3 in an AMPKdependent manner, in order to induce autophagy, cell cycle arrest and cell death in these cells 96, 108 .

Moreover, the knockdown of FOXO3 was sufficient to induce hypertrophy in cultured neonatal rat cardiomyocytes. In these cells, stimulation with insulin inhibits FOXO3 function, with subsequent downregulation of the antioxidant enzyme catalase and increased levels of ROS, that in low levels may act as second messengers for intracellular signaling, making possible the increase in cell size 109 . Atrogin 1, upregulated by FOXO1 and FOXO3, plays important roles in cardiovascular system, since mice lacking atrogin-1 are susceptible to cardiac hypertrophy 20 . FOXO proteins are inducing atrophy of differentiated cardiac and skeletal muscle cells through protein synthesis inhibition, which leads to a decrease in cell size 69 . In skeletal muscle, this mechanism involves myostatin, a FOXO transcriptional target and a secreted molecule that can induce atrophy by protein synthesis inhibition 110 .

FOXO1 might be implicated in the development or progression of type 2 diabetes, since increased FOXO1 expression in diabetic mouse liver is associated with increased expression of PEPCK and G6Pase, and inhibition of FOXO1 activity downregulated both PEPCK and G6Pase expression and normalized the blood glucose levels. Thus, FOXO1-mediated expression of G6Pase and PEPCK is critical for gluconeogenesis in the liver during fasting, but its deregulation may be involved in diabetes etiology 111 . Physiological functions of FOXO take place under certain circumstances, since sometimes the ability to maintain the proper control is overwhelmed 20 . Experiments on insulin-producing mouse pancreatic beta cells (betaTC-6) show that chronic exposure to high glucose activates FOXO transcription factors and leads to upregulation of endogenous inflammatory cytokines interleukin-1beta (IL-1beta) and suppressors of cytokine signalling (SOCS). These events trigger the activation of caspase-3 with subsequent apoptosis, suggesting a new mechanism that leads to the destruction of endocrine pancreas in type 2 diabetes 92 . Also, exposure to high glucose of the cardiac microvascular endothelial cells (CMECs) isolated from hearts of adult rats show that FOXO transcription factors leads to reactive oxygen species (ROS) accumulation and apoptosis, suggesting that FOXOs might be involved in microvascular complications of diabetes 93 . FOXO is also involved in insulin resistance and metabolic syndrome, since the activation of FOXO1 in cardiomyocytes leads to increased AKT activity and attenuated cellular response to insulin, followed by decreased glucose uptake 112 .

Interestingly, clinical studies regarding metabolic status profile on age-related diseases, fertility, fecundity and mortality revealed higher HbA1c levels and increased mortality risk associated with specific haplotypes of FOXO1 113 .

FOXO proteins are also activated in an attempt to protect the human body against the oxidative stress resulted due to hyperglycemia that leads to increased production of ROS in endothelial cells, liver cells, and pancreatic β-cells. This hyperglycemia-dependent ROS increase leads to a subsequent development of insulin resistance and significant neurodegenerative and cardiovascular diseases in the patients with diabetus mellitus 20 .

FOXOs are necessary for endothelial cell development and angiogenesis, since mice that are deficient in FOXO1 lack development of the vascular system and die by embryonic day eleven 114 . In addition, FOXO1 and FOXO3 were shown to be the most abundant FOXO isoforms in mature endothelial cells, having also an important role in the regulation of postnatal vessel formation, not only in the embryogenesis 36 . Unfortunately, angiogenesis is not only involved in critical physiological processes, such as embryogenesis and postnatal vessel formation, but it is also involved in pathological events, such as chronic inflammation and tumor growth 115 . Thus, it is fascinating how the angiogenesis mediated by FOXO proteins may become a negative element for the organism, antagonizing the tumor suppresor's main function through new vessel formation, that can lead to tumor cell growth 116 .

FOXO3 was associated with both cardiomyocyte survival after oxidative stress and heart muscle loss with subsequent ventricular dysfunction 43, 117 . FOXOs are activated after AKT inhibition by insulin or other factors, leading to Atrogin-1 induction, which results in a suppression of heart muscle cell size 43 .

FOXO3 proteins seem to inhibit the vascular smooth muscle cell proliferation and growth in a rat balloon carotid arterial injury model, suggesting a role of FOXOs in the regulation of vascular tone and systemic arterial blood pressure, preventing or at least lessening the effects of atherosclerosis and hypertension 118 .

Also, decreased FOXO1 expression due to high flow states in vessels leads to proliferation of vascular smooth muscle cells, vascular neointimal hyperplasia, and subsequent hypertension 45 . Moreover, experiments on lowdensity lipoprotein (Ldl) receptor knockout mice resulted in the prevention of atherosclerosis when the triple ablation of FOXO1, FOXO3 and FOXO4 was induced in endothelial cells 44 . Interestingly, the same experiment on myeloid cells lead to more severe atherosclerosis compared to the controls, explained by authors through increased proliferation of granulocyte-monocyte progenitors and high levels of inducible nitric oxide synthase (iNOS) and oxidative stress, which predispose to atherosclerosis 119 .

Noteworthy, analysis of mouse oocytes revealed overexpressed FOXO3 transcription factors in primordial and early primary follicles, but downregulated FOXO in primary and more developed follicles, suggesting that FOXO proteins also have reproductive functions, modulating oocyte and follicular cell maturation. To confirm the hypothesis, constitutively active FOXO3 was induced in transgenic mouse oocytes in primary and more developed follicles, which affected the oocyte growth and follicular development, leading to anovulation and luteinization of unruptured follicles, with subsequent infertility 46 . In addition, FOXO3 and FOXO1 mutations were detected in a small percentage of womens with premature ovarian failure 120 .

Involvement of FOXO family of transcription factors in stem cells self-renewal, survival, proliferation and differentiation is currently under investigation. FOXOs have been shown to play critical functions in maintaining self-renewal potential and quiescence of hematopoietic stem cells, however, the mechanisms of these processes are not yet well understood 1, 69 . Recent reports show that FOXO-mediated regulation of cell cycle, oxidative stress and apoptosis plays an important role in these processes 69 .

Stem cells are characterized by the capacity of self-renewing and the ability to differentiate 121 . They are necessary in maintenance and propagation of several adult tissues, including but not limited to blood, skin and gastro-intestinal epithelium. Adult stem cells or cells with stem cell properties were also found in other critical organs/systems, such as the central nervous system and the lung 69 .

Previous studies suggested that hematopoietic stem cells are sensitive to reactive oxygen species (ROS) levels. FOXO family members are known to play a central role in ROS detection and in inducing an adaptative response after ROS exposure, by inducing the expression of critical enzymes that neutralise ROS, such as catalase and manganase superoxide dismutase (MnSOD). Interestingly, FOXO1, FOXO3, and FOXO4 inactivation leads to an upregulation of ROS levels in hematopoietic stem cells and their death 121 .

Deletion of these three FOXO family members in mice revealed their importance in controlling ROS in stem cells, in vivo 27 . While the number of hematopoietic stem cells in bone marrow of FOXO-deficient mice is low, an increase in myeloid progenitor cells in blood is observed. Moreover, the repopulation ability is decreased in the absence of FOXOs and the treatment of FOXO-deficient mice with N-Acetylcysteine (NAC) at least partially rescued these effects 27 .

Thus, persistent AKT activation, which induces inactivation of FOXO transcription factors by AKT-mediated phosphorylation, results in ROS-induced cell death. This is due to the fact that the cells can't synthesize the FOXO-dependent ROS neutralizing factors catalase and MnSOD 121 . Between FOXO family members, the most important regulator of hematopoietc stem cells survival and self-renewal is FOXO3, since FOXO3 knockdown induces hematopoietic stem cells depletion 121 . ROS neutralizing agent N-Acetylcysteine (NAC) can rescue hematopoietic stem cells quiescence and at least partially resque their ROS-induced loss 121 . All these results suggest that FOXO1, FOXO3 and FOXO4-induced resistance to ROS is critical in maintaining homeostasis of hematopoietic stem cells in bone marrow 27 .

PTEN tumor suppressor was revealed as an important modulator of hematopoietic stem cells self-renewal and survival. PTEN is a major inhibitor of AKT activation. Depletion of PTEN, induces AKT activation and subsequent FOXO inactivation. It is likely that FOXOs mediate at least a part of the PTEN effects on hematopoietic stem cells 121 .

Although FOXO3 was established as the most important FOXO family member regulator of hematopoietic stem cell's self-renewal, FOXO1 is critical for the human embryonic stem cells (hESC) pluripotency maintenance. FOXO1induced SOX2 and OCT4 expression is one of the mechanisms responsible for this process. Interestingly, in embryonic stem cells AKT is not the major regulator of FOXO1 71 .

Fascinating, a recent study brings evidence that FOXO is a critical regulator of stem cell maintenance in Hydra vulgaris, a member of the phylogenetically old animal phyla Cnidaria, which has been suggested to be biologically immortal due to the unlimited self-renewal capacity of their stem cells 38, 122 .

FOXO transcription factors are not only required for maintenance of somatic stem cells, but they also play an important role in cancer stem cells 71 . Recent reports provided evidence that in many types of malignancies, such as leukemia, colon, or gastro-intestinal malignanciens, a small population of cells similar to stem cells exists 121 . These cells, called cancer stem cells, have the potential of forming new tumors. Notably, most of the time, the cancer stem cells are resistant to current cancer treatments, and these therapies may result in cancer stem cells enrichment. These cells serve as a starting point in cancer recurrence 121 . Similarities between stem cells and cancer stem cells were best described in the hematopoietic system, where similar surface markes and signal transduction patterns were described between the hematopoietic stem cells and leukemia-initiating cells 121 .

Presented results have not only implications in uncovering the stem cells/cancer stem cells regulation, self-renewal and differentiation, but also for the development of novel therapeutic strategies in cancer, degenerative diseases and many other pathologies 71 .

FOXO family members are expressed in almost every tissue of the human body, including the nervous system, cardiovascular system, reproductive system of males and females, lung, liver, spleen, pancreas, thymus, and skeletal muscle. However, each member of the FOXO family has its own expression pattern, since they are not equally expressed in all tissues 20 . FOXO1 is better represented in adipose tissue 27 . FOXO3 has the highest expression in liver, but it is also being predominantly expressed in heart, brain, kidneys, and ovaries, while FOXO4 is found mainly in the muscle and heart 20,27 . The newest member of the transcription family, FOXO6, is present in the brain. The association of this member with other tissues is still a matter of study 123 .

Cell lines (immortalized and/or cancer cells) are some of the most used and useful tools for studying the structure, function, regulation and expression of proteins in general, and FOXO family members in particular. FOXO members expression in different cell lines (including NCI 60 group of cell lines) is partially known 124, 125 . FOXO1 is found to be expressed at high levels in IGROV 1 (human ovarian carcinoma cells), astrocyte cells, RL 7 (human follicular lymphoma cells), HT29 (human colon carcinoma cells) and HEK 293 (human embryonic kidney cells). Knowing the qualitative and quantitative expression pattern of FOXO family members is important in elucidating their functions and regulation. Thus, databases summarizing these patterns in various tissues and cell lines are very helpful and necessary. For example, BioGPS presents experimental results showing the mRNA expression levels of a wide number of genes in most of the human tissues and many (mostly human) cell lines 126, 127, 128 .

Regulation of FOXOs expression is not yet well understood. P300 was shown to control FOXO1 gene expression by binding to the proximal region of the FOXO1 promoter (CRE tandem sites) 129 . Non-coding RNAs were shown to suppress translation of FOXO family members in various tissues and contexts. In particular, the microRNAs-dependent inhibition of FOXO1 and FOXO3 expression is better studied and is summariez below, in chapter 7.

However, the main transcription factors implicated in FOXOs expression are not well understood. Interestingly, methylation of FOX promotors induces suppression of their expression. As an example, promoter methylation induced by BRAF results in inactivation of FOX genes expression 130 .

The miRNAs are 18-28 nucleotide-long noncoding RNA molecules with an important role in post-transcriptional regulation of protein expression that regulate a variety of cellular processes, including cell differentiation, cell cycle progression and apoptosis. These miRNAs can function as oncogenes or tumor suppressors, and oncogenic miRNAs (oncomiRs) are upregulated in cancer cells. In cancer, miRNAs were found to be situated both upstream and downstream of the carcinogenesis process and modified expression of some miRNAs is the outcome of carcinogenic transformation or progression, revealing that miRNAs may be potential diagnostic or prognostic tools in cancer. 131 For instance, microRNAs gained a special attention in melanoma studies and the altered pattern of miRNA in melanoma seems to be related to apoptosis (miR-15b), cell cycle (miR-193b) and invasion/metastasis (miR-182) 132 .

The microRNA (miRNA)-mediated regulation of FOXO transcription factors was demonstrated by several groups within the last three years. miR-182 has been shown to specifically target FOXO transcription factors irrespective of cell type, since miR-182 seems to target FOXO3 in melanoma cells, FOXO1 in breast cancer cells and FOXO1 in activated helper T (Th) lymphocytes 90 . Thus, in melanoma cells, miR-182 modulate the expression of both FOXO3 and microphthalmia-associated transcription factor (MITF). The inhibition of miR-182 by anti-miRs (blocking antisense oligonucleotides) hindered melanoma cell migration and triggered their apoptosis 90 . In breast cancer cells, FOXO1 was coordinately targeted by miR-27a, miR-96, and miR-182, while the inhibition of each miRNA resulted in induced levels of FOXO1 and reduced breast cancer cell survival 90 . miR-182 also targets FOXO1 in osteoblasts lineage cells in order to inhibit osteoblast proliferation and differentiation, repressing the osteogenesis 133 .

Many other microRNAs were shown to regulate FOXOs activity and functions, including apoptosis or cell cycle. MiR-96 has been shown to regulate FOXO1-induced apoptosis in transitional cell carcinoma 134 . Also, increased expression of miR-96 in breast cancer cells have been shown to downregulate FOXO3 transcription factor with consequent induction of cell proliferation 135 . Also, increased miR-96, miR-182 and miR-183 downregulate the expression of FOXO1 transcription factor in classical Hodgkin lymphoma (cHL) cell lines, suggesting that decreased FOXO1 expression is involved in lymphomagenesis 136 . Moreover, a recent study performed on DU145 and LNCaP human prostate cancer cells show that upregulated microRNA-370 induces proliferation due to downregulation of the FOXO1 transcription factor 137 . In addition, miR-155, which is highly induced in mature activated T and B cells and in Treg cells, has recently been shown to target FOXO3 in T cells, but it remains to be shown whether FOXO3 via miR-155 contributes to the observed phenotypes in B and T lymphocytes 90 .

New strategies to modulate FOXO expression may now be developed since the discovery of miRNAs targeting FOXO transcription factors 90 . However, some difficulties may appear in the miRNA-based therapeutic manipulation of FOXO transcription factors. For example, a single miRNA may target hundreds of genes among FOXOs, and the therapeutic manipulation of a specific miRNA could have unanticipated adverse effects by influencing whole gene networks, while having only moderate effects on FOXO genes 90 . Since delivery of miR-182 mimics could induce lymphoproliferative disease or other forms of cancer by systemic repression of FOXO transcription factors, another challenge in the miRNA-FOXO therapeutic manipulation is the specific delivery of the miRNA into the target cell, in order to avoid adverse effects in other cell types or tissues 90 .

Several microRNAs were identified as being targets of FOXO transcription factors. An AKT -FOXO -miR-30d signaling pathway was recently identified. After inhibition of AKT, activated FOXO3 leads to upregulation of miR-30d. miR-30d acts as a tumor suppressor in renal cell carcinoma, further inhibiting the oncoprotein metadherin (MTDH) 138 .

Another recent study shows that FOXO1 stimulates the expression of a microRNA cluster located on a X chromosome, in a direct manner, dependent on RNA polymerase II, but not on the de novo protein synthesis. Thus, FOXO1 upregulates miR-506, miR-508, miR-513c, miR-513a-1, miR-513a-2. Also, the same study shows that inhibition of PI3K-AKT axis in LNCaP and MCF7 human carcinoma cell lines is followed by increased miR-506. As suggested by authors, miRNAs could be valuable biomarkers of FOXO activity 139 .

A study performed on primary cultures of neural stem/progenitor cells (NSPCs) from adult mice show that the expression levels of the miR-106b~25 cluster members (miR-106b, miR-93, and miR-25) is modulated by FOXO3 transcription factors in a complex manner 140 . The precursors of the miR-106b~25 cluster members are located on Mcm7 gene. FOXO3 directly binds to the first intron of this gene, modulating the expression of the microRNAs. Thus, FOXO3 transcription factors could be an important tool in preventing the loss of neurogenesis during aging 140 . Further studies are needed to completely understand the regulation of microRNAs expression by activated FOXO proteins.

FOXO transcription factors and tumor suppressors are ubiquitously expressed in the human body, with some specific differences between its members. As resumed above, FOXO proteins are characterized by a remarkable functional diversity, being implicated in regulation of many critical cellular functions, such as cell cycle arrest, apoptosis, oxidative detoxification, DNA damage repair, stem cell maintenance, cell differentiation, cell metabolism, angiogenesis, cardiac development, aging and others.

FOXO proteins play an important role not only during physiological cellular processes, but also in few pathologies, such as cancer. They are well known tumor suppressors proteins. Although FOXO proteins protect the human body by playing a central role in a wide range of mainly physiological functions, under some circumstances, FOXO's roles can become harmful for the human cells. This is because FOXO is also involved in a number of pathological functions, such as inflammation, muscle atropy, and a number of physiological functions that become harmful for the organism. For example, apoptosis places FOXO proteins on the good side when it leads to tumor suppression, but in some cases cellular apoptosis can become itself a significant component for pathology in diseases such as neurodegenerative disease, diabetes mellitus (DM), and cardiovascular injury.

Interestingly, while excessive FOXO levels induce cell cycle arrest and cell death, complete knock-down of FOXOs leads to cell cycle progression impairment, suggesting that certain levels of FOXO activation are required for cell cycle progression. Moreover, FOXO proteins play a variety of roles in the cells dependending on the context.

In 

Deciphering the role of forkhead transcription factors in cancer therapy

FoxO tumor suppressors and BCR-ABL-induced leukemia: a matter of evasion of apoptosis

SnapShot: forkhead transcription factors I

Sly as a FOXO": new paths with Forkhead signaling in the brain

The homeotic gene fork head encodes a nuclear protein and is expressed in the terminal regions of

Dynamic FoxO transcription factors

Forkhead transcription factors contribute to execution of the mitotic programme in mammals

Inflammatory arthritis requires Foxo3a to prevent Fas ligandinduced neutrophil apoptosis

FoxO transcription factors and stem cell homeostasis: insights from the hematopoietic system

FOXOs attenuate bone formation by suppressing Wnt signaling

FOXO1 is an essential regulator of pluripotency in human embryonic stem cells

The Fork head transcription factor DAF-16 transduces insulin-like metabolic and longevity signals in C. elegans

Insulin regulated hepatic gluconeogenesis through FOXO1-PGC-1alpha interaction

The forkhead transcription factor Foxo1 links insulin signaling to Pdx1 regulation of pancreatic beta cell growth

Forkhead transcription factor FoxO1 in adipose tissue tissue regulates energy storage and expenditure

Forkhead protein FoxO1 mediates Agrpdependent effects of leptin on food intake

Deletion of hepatic FoxO1/3/4 genes in mice significantly impacts on glucose metabolism through downregulation of gluconeogenesis and upregulation of glycolysis

Foxo1 mediates insulin action on apoC-III and triglyceride metabolism

Hepatic FoxOs regulate lipid metabolism via modulation of expression of the nicotinamide phosphoribosyltransferase gene

Minibrain/Dyrk1a regulates food intake through the Sir2-FOXO-sNPF/NPY pathway in Drosophila and mammals

FOXO3 regulates peroxiredoxin III expression in human cardiac fibro blasts

Regulation of sterol carrier protein gene expression by the forkhead transcription factor FOXO3a

DNA repair pathway stimulated by the forkhead transcription factor FOXO3a through the Gadd45 protein

DAF-16/FoxO Directly Regulates an Atypical AMP-Activated Protein Kinase Gamma Isoform to Mediate the Effects of Insulin/IGF-1 Signaling on Aging in Caenorhabditis elegans

Down-regulation of a forkhead transcription factor, FOXO3a, accelerate s cellular senescence in human dermal fibroblasts

Down-regulation of manganese-superoxide dismutase through phosphorylation of FOXO3a by Akt in explanted vascular smooth muscle cells from old rats

Akt negatively regulates the in vitro lifespan of human endothelial cells via a p53/p21-dependent pathway

Exercise training promotes SIRT1 activity in aged rats

Lymphocyte signaling: regulation of FoxO transcription factors by microRNAs

An essential role of the Forkhead-box transcription factor Foxo1 in control of T cellhomeostasis and tol erance

High glucose induces suppression of insulin signalling and apoptosis via upregulation of endogenous IL-1beta and suppressor of cytokine signalling-1 in mouse pancreatic beta cells

High glucose induced oxidative stress and apoptosis in cardiac microvascular endothelial cells are regulated by FoxO3a

APO2 ligand/tumor necrosis factor-related apoptosis-inducing ligand in prostate cancer therapy

Common mechanism for oncogenic activation of MLL by forkhead family proteins

Applications of post-translational modifications of FoxO family proteins in biological functions

FoxOs are lineage-restricted redundant tumor suppressors and regulate endothelial cell homeostasis

Decreased expression of the FOXO3a gene is associated with poor prognosis in primary gastric adenocarcinoma patients

The DNA damage repair protein Ku70 interacts with FOXO4 to coordinate a conserved cellular stress response

Therapy-resistant acute lymphoblastic leukemia (ALL) cells inactivate FOXO3 to escape apoptosis induction by TRAIL and Noxa

Induction of Mxi1-SR alpha by FOXO3a contributes to repression of Myc-dependent gene expression

Combination of bortezomib and mitotic inhibitors down-modulate Bcr-Abl and efficiently eliminates tyrosine-kinase inhibitor sensitive and resistant Bcr-Abl-positive leukemic cells

Foxo1 increased pro-inflammatory gene expression by inducing C/ EBPbeta in TNF-alpha-treated adipocytes

FoxO1 links insulin resistance to proinflammatory cytokine IL 1beta production in macrophages

Inhibition of FoxO transcriptional activity prevents muscle fiber atrophy during cachexia and induces hypertrophy

FoxO3 controls autophagy in skeletal muscle in vivo

FoxO3 coordinately activates protein degradation by the autophagic/lysosomal and proteasomal pathways in atrophying muscle cells

Inhibition of p38alpha unveils an AMPK-FoxO3A axis linking autophagy to cancer-specific metabolism

Foxo3a inhibits cardiomyocyte hypertrophy through transactivating catalase

Regulation of myostatin expression and myoblast differentiation by FoxO and SMADtranscription factors

Inhibition of Foxo1 function is associated with improved fasting glycemia in diabet ic mice

FoxO transcription factors activate Akt and attenuate insulin signaling in heart by inhibiting protein phosphatases

Haplotypes in the human Foxo1a and Foxo3a genes; impact on disease and mortality at old age

Abnormal angiogenesis in Foxo1 (Fkhr)-deficient mice

Multifaceted link between cancer and inflammation

Constitutive phosphorylation of the FOXO1 transcription factor in gastric cancer cells correlates with microvessel area and the expressions of angiogenesis -related molecules

FoxO transcription factors promote cardiomyocyte survival upon induction of oxidative stress

Forkhead transcription factors inhibit vascular smooth muscle cell proliferation and neointimal hyperplasia

Expanded granulocyte/monocyte compartment in myeloid-specific triple FoxO knockout increases oxidative stress and accelerates atherosclerosis in mice

Mutational screening of FOXO3A and FOXO1A in women with premature ovarian failure

The PI-3kinase pathway in hematopoietic stem cells and leukemia-initiating cells: a mechanistic difference between normal and cancer stem cells

Mortality pattern suggest lack of senescence in hydra

FOXOs: signalling integrators for homeostasis maintenance

Modulators of sensitivity and resistance to inhibition of PI3K identified in a pharmacogenomic screen of the NCI-60 human tumor cell line collection

Global proteome analysis of the NCI-60 cell line panel

BioGPS: an extensible and customizable portal for querying and organizing gene annotation resources

BioGPS and MyGene.info: organizing online, gene-centric information

A gene atlas of the mouse and human protein-encoding transcriptomes

Control of Foxo1 Gene Expression by Co-activator P300

BRAF mutation-specific promoter methylation of FOX genes in colorectal cancer

Tissular and soluble miRNAs for diagnostic and therapy improvement in digestive tract cancers

Immune-related biomarkers for diagnosis/prognosis and therapy monitoring of cutaneous melanoma

miR-182 is a negative regulator of osteoblast proliferation, differentiation, and skeletogenesis through targeting FoxO1

miR-96 regulates FOXO1-mediated cell apoptosis in bladder cancer

Unregulated miR-96 induces cell proliferation in human breast cancer by downregulating transcriptional factor FOXO3a

FOXO1 is a tumor suppressor in classical Hodgkin lymphoma

Upregulation of MircoRNA-370 induces proliferation in human prostate cancer cells by downregulating the transcription factor FOXO1

Akt/FOXO pathway in renal cell carcinoma

FOXO1 regulates expression of a microRNA cluster on X chromosome

The microRNA cluster miR-106b~25 regulates adult neural stem/progenitor cell proliferation and neuronal differentiation