Novel aminotetrazole derivatives as selective STAT3 non-peptide inhibitors

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TitreNovel aminotetrazole derivatives as selective STAT3 non-peptide inhibitors
Type de publicationJournal Article
Year of Publication2015
AuteursPallandre J-R, Borg C, Rognan D, Boibessot T, Luzet V, Yesylevskyy S, Ramseyer C, Pudlo M
JournalEUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
Volume103
Pagination163-174
Date PublishedOCT 20
Type of ArticleArticle
ISSN0223-5234
Mots-clésAminotetrazole, Anticancer drug, inflammation, Small-molecule inhibitor, STAT3
Résumé

The development of inhibitors blocking STAT3 transcriptional activity is a promising therapeutic approach against cancer and inflammatory diseases. In this context, the selectivity of inhibitors against the STAT1 transcription factor is crucial as STAT3 and STAT1 play opposite roles in the apoptosis of tumor cells and polarization of the immune response. A structure-based virtual screening followed by a luciferase-containing promoter assay on STAT3 and STAT1 signaling were used to identify a selective STAT3 inhibitor. An important role of the aminotetrazole group in modulating STAT3 and STAT1 inhibitory activities has been established. Optimization of the hit compound leads to 23. This compound inhibits growth and survival of cells with STAT3 signaling pathway while displaying a minimal effect on STAT1 signaling. Moreover, it prevents lymphocyte T polarization into Th17 and Treg without affecting their differentiation into Th1 lymphocyte. (C) 2015 Elsevier Masson SAS. All rights reserved.

DOI10.1016/j.ejmech.2015.08.054