key: cord-0768866-0kawnivh
authors: Plens-Gałąska, Martyna; Woźniak, Tomasz; Wesoły, Joanna; Bluyssen, Hans A. R.
title: SINBAD, structural, experimental and clinical characterization of STAT inhibitors and their potential applications
date: 2022-03-31
journal: Sci Data
DOI: 10.1038/s41597-022-01243-3
sha: 97fcdf527bda0c930219580a13d5dbe0bb713848
doc_id: 768866
cord_uid: 0kawnivh

The abnormal activation of signal transducer and activator of transcription (STAT) protein family is recognized as cause or driving force behind multiple diseases progression. Therefore, searching for potential treatment strategy is pursued by multiple scientific groups. We consider that providing comprehensive, integrated and unified dataset for STAT inhibitory compounds may serve as important tool for other researchers. We developed SINBAD (STAT INhbitor Biology And Drug-ability) in response to our experience with inhibitory compound research, knowing that gathering detailed information is crucial for effective experiment design and also for finding potential solutions in case of obtaining inconclusive results. SINBAD is a curated database of STAT inhibitors which have been published and described in scientific articles providing prove of their inhibitory properties. It is a tool allowing easy analysis of experimental conditions and provides detailed information about known STAT inhibitory compounds.

compounds, especially exploring the interaction area of the SH2 domain and the phosphorylated tyrosine residue, yielded many synthetic small molecules (over 100 compounds). Among the most potent are STA-21, STATTIC, STX-0119 and OPB-31121 [4] [5] [6] [7] . Other types of inhibitors include natural products (eg. Resveratrol and its analogues -Piceatannol and LYR71, Curcumin) peptides and peptidomimetics (CJ-1383, BP-PM, PM-73), oligodeoxynucleotide decoys and antisense oligonucleotides [8] [9] [10] [11] [12] .

Identification of specific and effective STAT inhibitory strategies could provide a tool to increase our understanding of their functional role in different diseases. Moreover, promising results for several STAT inhibitors in recent clinical trials predicts STAT-inhibiting strategies may find their way to the clinic, and could serve as therapeutic strategies in cancer, inflammation, autoimmunity and viral infections. Since December, 2019, a disease outbreak caused by a novel coronavirus (SARS-CoV-2) was declared a global public health emergency by WHO and named coronavirus infected disease-19 (COVID- 19) 13 . Dysregulated host immune responses and robust production of inflammatory cytokines and interferons, known as the "cytokine storm", correlate with disease severity and poor prognosis during SARS-CoV2 infection 14 . Since many of these factors are potent activators of STAT signaling pathways, this identifies STATs as potential therapeutic targets in COVID-19 disease as well. Anti-IL6 antibodies, as well as JAK inhibitors (indirect STAT inhibitors)-Baricitinib, Fedratinib, and Ruxolitinib have already been selected as part of a potential treatment strategy against COVID-19 as a combined antiviral and anti-inflammatory approach [15] [16] [17] [18] [19] . Ruxolitinib entered phase III clinical trial (NCT04120090, NCT03533790) and Fedratinib phase II, both were used in pneumonia associated COVID-19 cases.

The relevance of STATs as therapeutic targets is emphasized by the numerous studies and publications of STAT inhibitors, involving multiple in silico, in vitro, ex vivo, in vivo methods, in different experimental settings and disease models and the inclusion of a number of these inhibitors in clinical trials. With our database we provide a comprehensive tool for detailed characterization of compounds disrupting STAT signaling in various conditions allowing better understanding of their nature and mode of action. In addition, our database can be a source of information for other groups and function as primary selection tools for potential known inhibitors for further investigation in SARS-CoV-2 research.

Data collection. We created the SINBAD Database following guidelines described by the FAIR data principles 20 . An initial inhibitor list was created based on a collection of review articles selected in the search described below. This was followed by manual selection of suitable research manuscripts which further were divided into small groups based on the described inhibitors. Using scientific search engines -National Center for Biotechnology Information (NCBI) -PubMed and Google Scholar, firstly we focused on gathering names of known STAT inhibitory compounds. For this purpose, we initially used available Review articles which summarized STAT inhibitory strategies with a description of exemplary inhibitors, many of which focused on cancer research. This was followed by using more advanced search and phrase-base options: "("stat1 inhibitor") OR ("stat2 inhibitor") OR ("stat3 inhibitor") OR ("stat4 inhibitor") OR ("stat5 inhibitor") OR ("stat5a inhibitor") OR ("stat6 inhibitor") OR ("stat1 inhibition") OR ("stat2 inhibition") OR ("stat3 inhibition") OR ("stat4 inhibition") OR ("stat5 inhibition") OR ("stat5a inhibition") OR ("stat6 inhibition"). In this way, from PubMed we extracted 1559 potential literature sources for our database. Additionally, we checked separately every compound by its name in both NCBI PubMed and Google Scholar. This approach allowed us to thoroughly screen available literature, followed by initial manual screening of each publication and further selection and proper grouping (Fig. 1a ). In the SINBAD database, we decided to include inhibitors: small compounds, antibodies, peptides, peptidomimetics, oligonucleotides which interact directly with STAT proteins but also those which may influence STATs indirectly by interacting with other proteins for instance targeting JAK kinases or multiple interferon or interleukin receptors. Where possible we provided information about which protein or which protein domain was targeted or was proposed to interact with the inhibitor. In case where we could not find detailed data, we used more general terms eg. "JAK-STAT inhibition", "JAK inhibitor", "STAT downregulation", or did not provide any information. In case of a proven interaction of the inhibitor with the STAT-SH2 domain, we provided additional docking visualization (Fig. 1c ) by using the Surflex-Dock 2.6 program in combination with STAT 3D models which were previously published by or group 21 . What is more, we decided to include information from publications which described only STAT inhibition and to omit publications which predominantly focused on other proteins, transcription factors or pathways. This approach allowed us to build an initial inhibitor list consisting of approximately 100 STAT inhibitors and then by further investigation we composed a final list with 144 positions described in over 200 publications (Fig. 1a) .

Database design. The datasets generated and analyzed in this study are available at http://sinbad.amu.edu.pl as well as through public repository https://doi.org/10.6084/m9.figshare.14975136.v1 22 . In SINBAD, we collected crucial experimental data describing detailed characteristics of each individual inhibitor. Datasets can be obtained either via SINBAD webpage or via Figshare Repository. The Repository has folder structure. The code is available via the paths 'stat_project/stat_database' and 'stat_project/apps' , both containing python files creating the project additionally through the path 'stat_project/templates' we provide access to.html files. All of the additional files and external libraries used for the graph management, table visualization are located in 'static' folder. The data itself is localized in 'stat_projectpps\stats\management\data' and 'stat_project/media' containing Excel file with tables on which the database is built, and all used structural representations respectively. (Fig. 1b) instead of one. This approach allowed us to describe in more detail the experiment itself and to distinguish between different conditions/parameters, for example apoptosis may be monitored by various types of experiments such as Western blot, Flow cytometry, MTT or MTS assays. Western blot, on the other hand, is a widely used technique that illustrates protein activity in various cells and tissues. Together these variables create an easy and user-friendly way to delve into the details of each publication and compare presented results in a comprehensive way. Two smaller tables REFERENCES and VENDORS provide links to NCBI PubMed, title of publication, unique DOI number and PMC ID (REF_ID, REF_COMPOUND, REF_URL, REF_DOI, REF_TITLE) and links to potential vendor web pages (VEN_ID, VEN_COMPOUND, VEN_COMPANY). To provide a more complete picture, in the CLINICAL_TRIALS table, for some compounds we present data regarding clinical trials that have been performed and documented (over 16500 trials). Within this table we gathered basic information www.nature.com/scientificdata www.nature.com/scientificdata/ such as unique number of conducted trial (CLT_NCT_NUMBER) followed by current trial status and phase (CLT_STATUS, CLT_PHASE). Further we provide data regarding title of the conducted study and investigated diseases (CLT_STUDY_TITLE, CLT_CONDITIONS) and a link to the full report from the conducted study (CLT_URL). Of course, only some inhibitors were pursued into clinical trials, therefore clinical trial data is available only for a few of presented inhibitors. Furthermore, in DISEASE table, we compiled information from the same sources as used for the other tables about potential disease treatment strategies in which the inhibitor of interest was used (DIS_DISEASE_NAME, DIS_DISEASE_TYPE).

For the database creation we used Django web framework, Docker for efficient deployment, Nginx as web server, Elasticsearch as a search engine and finally MariaDB as SQL database.

The SINBAD database provides multiple options of filtering or searching depending on the individual users' preference -it can be used as a dataset downloaded on a personal computer and managed with R, Excel or used online. With SINBAD the user can address multiple questions regarding STAT inhibition and conditions in which it was tested (exemplary webpage layout described in Supplementary Data and shown in Supplementary  Fig. 1 ). It will allow to establish better conditions for future experiments and prevent repeating already existing data. In Fig. 2 we show exemplary questions which can be answered with SINBAD. If the User wants to retrieve all available data about a specific compound he/she has to choose at the homepage either COMPOUND in the left Menu panel or the molecule symbol on that page (Fig. 2a, Step 1 ). This will transfer the User to the table summarizing inhibitory compounds gathered in the database.

Step 2 -using either filtering options, type the name of the compound in the search window (marked with arrow) or choose compound from the list below (Fig. 2a, Step2) . On the other hand, if the User wants to investigate which compounds were tested in HeLa cell line at 50μM concentration, he/she has to choose at the homepage either EXPERIMENTS in the left Menu panel or the Dish symbol on this page (Fig. 2b, Step 1 ). This will transfer the User to the table summarizing experimental data gathered in the database.

Step 2 -using filtering options, type the cell line name -marked as 1, and concentration in proper filter window -marked as 3 (Fig. 2b, Step 2). Finally, if the User wants to search for data for a compound that entered Phase I clinical trials for breast cancer, he/she has to choose CLINICAL TRIALS (Fig. 2c, Step 1 ). This will transfer the User to the table summarizing clinical trial data gathered for inhibitory compounds.

Step 2 -using filtering options type number of phase of interest in window marked as 1. and specify condition using filter marked as 2 (Fig. 2c, Step 2) .

The SINBAD database is constantly being updated by the administrator of our group. What is more, it is possible for external users to upload their own published results, for which we provided a simple procedure. The User can request to add their own published data through a special contact form through which the User will receive access to a dedicated uploading panel. However, unpublished data will first have to be verified and approved by the administrator. One limitation of our dataset is that it does not include publications focusing on non-STAT target proteins. We are aware that there are multiple publications covering inhibitory properties of presented inhibitors that target pathways other than JAK-STAT. We are planning to expand SINBAD with additional experimental data gathered form publications focusing on non-STAT targets, including transcription factors such as IRFs, NF-κB and others.

All generated code and data are hosted within Figshare repository https://doi.org/10.6084/m9.figshare.14975136.v1 22 .

STATs and IRFs: Mediators of inflammation and therapeutic targets in cardiovascular disease

Therapeutic modulators of STAT signalling for human diseases

Transcription Factor Inhibition: Lessons Learned and Emerging Targets

A low-molecular-weight compound discovered through virtual database screening inhibits Stat3 function in breast cancer cells

A new small-molecule Stat3 inhibitor

Identification of a New Series of STAT3 Inhibitors by Virtual Screening

OPB-31121, a novel small molecular inhibitor, disrupts the JAK2/STAT3 pathway and exhibits an antitumor activity in gastric cancer cells

Beneficial effects of resveratrol administration-Focus on potential biochemical mechanisms in cardiovascular conditions

The immunomodulatory and anti-inflammatory role of polyphenols

Identification of a natural product-like STAT3 dimerization inhibitor by structure-based virtual screening

Small molecule inhibitors of Stat3 signaling pathway

Molecular docking studies on inhibition of Stat3 dimerization by curcumin natural derivatives and its conjugates with amino acids

NOTE: This preprint reports new research that has not been certified by peer review and should not be used to guide clinical practice

The cytokine storm of COVID-19: a spotlight on prevention and protection

JAK Inhibition as a New Treatment Strategy for Patients with COVID-19

TH17 responses in cytokine storm of COVID-19: An emerging target of JAK2 inhibitor Fedratinib

JAKs to STATs: A tantalizing therapeutic target in acute myeloid leukemia

The promise of jak inhibitors for treatment of sarcoidosis and other inflammatory disorders with macrophage activation: A review of the literature

The potential of JAK/STAT pathway inhibition by ruxolitinib in the treatment of COVID-19

Comment: The FAIR Guiding Principles for scientific data management and stewardship

Identification of STAT1 and STAT3 specific inhibitors using comparative virtual screening and docking validation

The authors confirm that this article content has no conflicts of interest. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

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