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BioAssay: AID 1805

Summary of probe development efforts to identify activators of signal transducer and activator of transcription 3 (STAT3)

Name: Summary of probe development efforts to identify activators of signal transducer and activator of transcription 3 (STAT3) ..more
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 Tested Compounds
 Tested Compounds
All(1)
 
 
Probe(1)
 
 
Active(1)
 
 
 Tested Substances
 Tested Substances
All(2)
 
 
Probe(2)
 
 
Active(2)
 
 
AID: 1805
Data Source: The Scripps Research Institute Molecular Screening Center (STAT3_ACT_LEADS_SUMMARY)
BioAssay Type: Summary, Candidate Probes/Leads with Supporting Evidence
Depositor Category: NIH Molecular Libraries Probe Production Network
BioAssay Version:
Deposit Date: 2009-06-05
Modify Date: 2010-07-13

Data Table ( Complete ):           Active    All
Target
Sequence: STAT3 [Homo sapiens]
Description ..   
Protein Family: Src homology 2 (SH2) domain

Gene:STAT3     Related Protein 3D Structures     More BioActivity Data..
BioActive Compound: Chemical Probe: 1    Active: 1
Depositor Specified Assays
AIDNameTypeComment
871Primary cell-based high throughput screening assay to measure STAT3 activationscreeningPrimary screen (STAT3 activators in singlicate)
932Primary cell-based high throughput screening assay to measure STAT1 activationscreeningPrimary screen (STAT1 activators in singlicate)
1267Confirmation cell-based high throughput screening assay to measure STAT3 activationscreeningConfirmation screen (STAT3 activators in triplicate)
1309Counterscreen assay for STAT3 activators: Cell-based high throughput assay to measure NF-kappaB activationscreeningCounterscreen (NF-kappaB activators in triplicate)
1318Counterscreen assay for STAT3 activators: Cell-based high throughput assay to measure STAT1 activationscreeningCounterscreen (STAT1 activators in triplicate)
1398Dose response cell-based assay to measure STAT3 activationconfirmatoryDose response (STAT3 activation in singlicate)
1406Dose response counterscreen assay for STAT3 activators: cell-based high throughput assay to measure STAT1 activationconfirmatoryDose response counterscreen (STAT1 activators in triplicate)
2049Late stage results from the probe development effort to identify activators of signal transducer and activator of transcription 3 (STAT3).screeningLate stage results (STAT3 activators)
Description:
Source (MLSCN Center Name): The Scripps Research Institute Molecular Screening Center
Center Affiliation: The Scripps Research Institute (TSRI)
Assay Provider: David Frank, Dana Farber Cancer Institute
Network: Molecular Library Screening Center Network (MLSCN)
Grant Proposal Number: 1 X01 MH079826-01
Grant Proposal PI: David Frank, Dana Farber Cancer Institute
External Assay ID: STAT3_ACT_LEADS_SUMMARY

Name: Summary of probe development efforts to identify activators of signal transducer and activator of transcription 3 (STAT3)

Description:

The signal transducer and activator of transcription (STAT) family of transcription factors transduce signals from a variety of extracellular stimuli and are important mediators of inflammation, cell survival, differentiation, and proliferation (1, 2). STATs are activated in response to growth factors, cytokines, and G-CSF binding to cell surface receptor tyrosine kinases (1-3). In resting cells STATs are inactive in the cytoplasm. In response to stimuli, STATs are phosphorylated by the Janus-activated kinases (Jaks), which induces STAT dimerization and nuclear translocation, where STATs bind to specific enhancer elements in target genes (2). Although structurally similar, the seven STAT family member (STATs 1, 2, 3, 4, 5a, 5b, and 6) possess diverse biological roles (2). For example, STAT1 activation is pro-inflammatory and anti-proliferative, while STAT3 activation is anti-inflammatory and pro-apoptotic (2). STAT1 is largely responsible for mediating the effects of IFN- γ, while STAT3 is predominantly involved in IL-6 signaling (4). STAT1 induces expression of genes that inhibit the cell cycle, and thus STAT1 is considered to have tumor suppressor properties (5). Studies show that STAT3 is activated in a majority of breast and prostate cancers, and that STAT3 inhibition using RNA interference or a dominant negative leads to reduced cell proliferation, survival, and wound healing (1, 4, 6). Blocking STAT3 interaction with the epidermal growth factor receptor (EGFR) using peptide aptamers has been shown to reduce tumor growth (7). Due to the diverse roles and potent phenotypes associated with STAT signaling, the identification of selective modulators of STAT3 activity may lead to pharmacological tools for cancer, wound healing, and inflammatory diseases.

Summary of Probe Development Effort:

Following primary HTS in singlicate to identify STAT3 activators (AID 871), confirmation of hit activity in triplicate (AID 1267), counterscreening in triplicate against NFkB (AID 1309) and STAT3 (AID 1318) to determine selectivity, followed by titration assays to determine compound potency (AID 1398) and selectivity (AID 1406), a compound belonging to the oxazole carboxamide scaffold was identified: SID 14735210 (liquid)/SID 87334054 (powder)/SID 87326010 (powder). This compound does not share structural similarities with the known STAT3 activator Compound 1 (8). Analogs were purchased in powder form or re-ordered from the MLSMR in liquid form and tested in dose response assays against both STAT3 and STAT1, as well as additional counterscreening assays using HT-1080 and NIH 3T3 cell lines to determine cytotoxicity. SID 87334054/SID 87326010 confirmed activity and is claimed as a potent, selective, and non-toxic STAT3 activator probe.

The above probe development effort resulted in the identification of one probe. A probe report has been published (http://mlpcn.florida.scripps.edu/index.php/probes/probe-reports.html). A probe report for SID 87334054/SID 87326010 can be found in the Molecular Libraries Bookshelf (PubMed Books) (http://www.ncbi.nlm.nih.gov/books) under ML115.

References:

1. Alvarez JV, Febbo PG, Ramaswamy S, Loda M, Richardson A, Frank DA. Identification of a genetic signature of activated signal transducer and activator of transcription 3 in human tumors. Cancer Res. 2005 Jun 15;65(12):5054-62.
2. Schindler C, Levy DE, Decker T. JAK-STAT signaling: from interferons to cytokines. J Biol Chem. 2007 Jul 13;282(28):20059-63.
3. Germain D, Frank DA. Targeting the cytoplasmic and nuclear functions of signal transducers and activators of transcription 3 for cancer therapy. Clin Cancer Res. 2007 Oct 1;13(19):5665-9.
4. Levy DE, Darnell JE Jr. Stats: transcriptional control and biological impact. Nat Rev Mol Cell Biol. 2002 Sep;3(9):651-62.
5. Battle TE, Wierda WG, Rassenti LZ, Zahrieh D, Neuberg D, Kipps TJ, Frank DA. In vivo activation of signal transducer and activator of transcription 1 after CD154 gene therapy for chronic lymphocytic leukemia is associated with clinical and immunologic response. Clin Cancer Res. 2003 Jun;9(6):2166-72.
6. Takeda, K. Takeda K, Kaisho T, Yoshida N, Takeda J, Kishimoto T, Akira S.1998. Stat3 activation is responsible for IL-6-dependent T cell proliferation through preventing apoptosis: generation and characterization of T cell- specific Stat3-deficient mice. J. Immunol. 161:4652-4660.
7. Buerger C, Nagel-Wolfrum K, Kunz C, Wittig I, Butz K, Hoppe-Seyler F, Groner B. Sequence-specific peptide aptamers, interacting with the intracellular domain of the epidermal growth factor receptor, interfere with Stat3 activation and inhibit the growth of tumor cells. J Biol Chem. 2003 Sep 26;278(39):37610-21.
8. Sakai R, Nakamura T, Nishino T, Yamamoto M, Miyamura A, Miyamoto H, Ishiwata N, Komatsu N, Kamiya H, Tsuruzoe N. Xanthocillins as thrombopoietin mimetic small molecules. Bioorg Med Chem. 2005 Dec 1;13(23):6388-93. Epub 2005 Aug 22.

Keywords:

Summary AID, STAT3, signal transducer and activator of transcription 3, acute-phase response factor, APRF, activation, activator, potentiation, potentiator, U3A, transcription factor, luciferase, luminescence, reporter, dose response, counterscreen, 1536, HTS, assay, Scripps, Scripps Florida, Scripps Research Institute Molecular Screening Center, SRIMSC, Molecular Libraries Probe Production Centers Network, MLPCN.
Protocol
Please see Relate Bioassays for protocols performed in this probe development effort.
Comment
Probes were identified.
Result Definitions
TIDNameDescriptionHistogramTypeUnit
OutcomeThe BioAssay activity outcomeOutcome
ScoreThe BioAssay activity ranking scoreInteger
1ML #Unique alphanumeric identifier assigned to a chemical probe molecule within the Molecular Libraries Probe Production Centers Network (MLPCN).String
Additional Information
Grant Number: 1 X01 MH079826-01

Data Table (Concise)
Classification
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