| Literature DB >> 33906046 |
Ziqian Wang1, Ting Song2, Zongwei Guo3, Laura B Uwituze1, Yafei Guo3, Hong Zhang3, Hang Wang3, Xiaodong Zhang1, Hao Pan1, Tong Ji1, Fangkui Yin1, Sheng Zhou1, Jian Dai1, Zhichao Zhang4.
Abstract
Targeting cancer-related Hsp70-Bim protein-protein interactions (PPIs) offers a new strategy for the design of Hsp70 inhibitors. Herein, we discovered a novel Hsp70 inhibitor, S1g-6, based on the established BH3 mimetics. S1g-6 exhibited sub-μM binding affinity toward Hsp70 and selectively disrupted Hsp70-Bim PPI. The target specificity of S1g-6in situ was validated by affinity-based protein profiling, co-immunoprecipitation, and cell-based shRNA assays. S1g-6 specifically antagonized the ATPase activity of Hsp70 upon recruiting Bim and showed selective apoptosis induction in some cancer cell lines over normal ones through suppression of some oncogenic clients of Hsp70, representing a new class of antitumor candidates. Hsp70-Bim PPI exhibited cancer-dependent role as a potential anti-cancer target.Entities:
Keywords: Antitumor candidate; Cancer-related target; Hsp70 inhibitor; Hsp70-bim PPI
Year: 2021 PMID: 33906046 DOI: 10.1016/j.ejmech.2021.113452
Source DB: PubMed Journal: Eur J Med Chem ISSN: 0223-5234 Impact factor: 6.514