| Literature DB >> 31607564 |
Ke Huang1, Qian Liang2, Ye Zhou2, Lu-Lu Jiang1, Wei-Ming Gu2, Ming-Yu Luo2, Ya-Bin Tang2, Yang Wang2, Wei Lu3, Min Huang4, Sheng-Zhe Zhang5, Guang-Lei Zhuang5, Qing Dai6, Qian-Cheng Shen7, Jian Zhang7, Hui-Min Lei2, Liang Zhu2, De-Yong Ye1, Hong-Zhuan Chen8, Lu Zhou9, Ying Shen10.
Abstract
Phosphoglycerate mutase 1 (PGAM1) plays a pivotal role in cancer metabolism and tumor progression via its metabolic activity and interaction with other proteins like α-smooth muscle actin (ACTA2). Allosteric regulation is considered to be an innovative strategy to discover a highly selective and potent inhibitor targeting PGAM1. Here, we identified a novel PGAM1 allosteric inhibitor, HKB99, via structure-based optimization. HKB99 acted to allosterically block conformational change of PGAM1 during catalytic process and PGAM1-ACTA2 interaction. HKB99 suppressed tumor growth and metastasis and overcame erlotinib resistance in non-small-cell lung cancer (NSCLC). Mechanistically, HKB99 enhanced the oxidative stress and altered multiple signaling pathways including the activation of JNK/c-Jun and suppression of AKT and ERK. Collectively, the study highlights the potential of PGAM1 as a therapeutic target in NSCLC and reveals a distinct mechanism by which HKB99 inhibits both metabolic activity and nonmetabolic function of PGAM1 by allosteric regulation.Entities:
Keywords: allosteric inhibitor; antitumor activity; metastasis; non-small-cell lung cancer; phosphoglycerate mutase 1
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Year: 2019 PMID: 31607564 DOI: 10.1016/j.cmet.2019.09.014
Source DB: PubMed Journal: Cell Metab ISSN: 1550-4131 Impact factor: 27.287