Synthesis and biological evaluation of tetrahydropyridinepyrazoles ('PFPs') as inhibitors of STAT3 phosphorylation

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Revanna, C.N. and Basappa, . and Srinivasa, V. and Feng Li, . and Kodappully Sivaraman Siveen, . and Xiaoyun Dai, . and Shivananju Nanjunda Swamy, . and Bhadregowda, D.G. and Gautam Sethi, . and Mantelingu, . and Andreas Bender, . and Rangappa, K.S. (2014) Synthesis and biological evaluation of tetrahydropyridinepyrazoles ('PFPs') as inhibitors of STAT3 phosphorylation. MEDCHEMCOMM, 05 (01). pp. 32-40. ISSN 2040-2511

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Official URL: https://doi.org/10.1039/c3md00119a

Abstract

The transcription factor STAT3 is constitutively overexpressed in many human tumors and hence represents a putative target for anticancer drug design. In this work, we describe the synthesis and biological evaluation of a novel chemotype, pyridine-fused pyrazoles ('PFPs') as inhibitors of STAT3 phosphorylation. The effect of the compounds synthesized was evaluated in cell proliferation assays of MCF-7 and HepG2 cancer cell lines and two of the compounds tested (12g and 12k) were found to show significant activity. Both compounds were also found to inhibit the proliferation of Hep3B, HUH-7 and PLC/PRF5 HCC cells in a dose-and time-dependent manner. Furthermore, we established in a DNA binding assay that one of the compounds (12g) was able to significantly inhibit the DNA binding ability of STAT3. Cytotoxicity of 12g against PC3 cells, which do not constitutively phosphorylate STAT3, was found to be minimal, hence lending further support for our mode-of-action hypothesis of this compound. We established for this structure a complete inhibition of CXCL12-induced cell invasion and associated wound healing in HCCLM3 cells, corroborating the proposed modulation of the STAT3 axis by 12g. Finally, molecular modeling was employed to evaluate the hypothesis of PFPs to bind to the SH2 domain of STAT3. Given the efficacy of PFPs in the biological systems studied here we propose their further evaluation in the context of STAT3-mediated cancer therapy.

Item Type: Article
Uncontrolled Keywords: TYROSINE KINASE INHIBITOR; CANCER DRUG DISCOVERY; SIGNALING PATHWAY; CELLS; ACTIVATION; TRANSDUCER; PROTEINS; TARGETS; DERIVATIVES; GROWTH
Subjects: Faculty of Science > Pure Sciences > Chemistry
Divisions: Jnana Bharathi / Central College Campus > Department of Chemistry
Depositing User: Mr H.G. Srikanth
Date Deposited: 24 Oct 2016 07:39
Last Modified: 24 Oct 2016 07:39
URI: http://eprints-bangaloreuniversity.in/id/eprint/6886

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