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Identification of Small Molecule Modulators of Gene Transcription with Anticancer Activity
Author(s) -
Tram Anh T. Tran,
Jennifer Wichterman-Kouznetsova,
Diana Varghese,
Ruili Huang,
Wenwei Huang,
Matthias Becker,
Christopher P. Austin,
James Inglese,
Ronald L. Johnson,
Elisabeth D. Martínez
Publication year - 2014
Publication title -
acs chemical biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.899
H-Index - 111
eISSN - 1554-8937
pISSN - 1554-8929
DOI - 10.1021/cb500532x
Subject(s) - derepression , epigenetics , biology , gene expression , regulation of gene expression , gene , small molecule , transcription factor , histone , viability assay , reporter gene , microbiology and biotechnology , computational biology , genetics , cell , psychological repression
Epigenetic regulation of gene expression is essential in many biological processes, and its deregulation contributes to pathology including tumor formation. We used an image-based cell assay that measures the induction of a silenced GFP-estrogen receptor reporter to identify novel classes of small molecules involved in the regulation of gene expression. Using this Locus Derepression assay, we queried 283,122 compounds by quantitative high-throughput screening evaluating compounds at multiple concentrations. After confirmation and independent validation, the Locus Derepression assay identified 19 small molecules as new actives that induce the GFP message over 2-fold. Viability assays demonstrated that 17 of these actives have anti-proliferative activity, and two of them show selectivity for cancer versus patient-matched normal cells and cause unique changes in gene expression patterns in cancer cells by altering histone marks. Hence, these compounds represent chemical tools for understanding the molecular mechanisms of epigenetic control of transcription and for modulating cell growth pathways.

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