| Literature DB >> 27829129 |
Wei Li1, Xiaoqian Ma1, Na Li1, Huasheng Liu1, Qiong Dong1, Juan Zhang1, Cejun Yang1, Yin Liu1, Qi Liang1, Shengwang Zhang1, Chang Xu1, Wei Song2, Shiming Tan3, Pengfei Rong1, Wei Wang4.
Abstract
Deregulation of glycolysis was often observed in human cancer cells. In the present study, we reported resveratrol, a small polyphenol, which has been intensively studied in various tumor models, has a profound anti-tumor effect on human non-small cell lung cancer (NSCLC) via regulation of glycolysis. Resveratrol impaired hexokinase II (HK2)-mediated glycolysis, and markedly inhibited anchorage-dependent and -independent growth of NSCLC cells. Exposure to resveratrol decreased EGFR and downstream kinases Akt and ERK1/2 activation. Moreover, we revealed that resveratrol impaired glucose metabolism by mainly inhibiting expression of HK2 mediated by the Akt signaling pathway, and exogenous overexpression of constitutively activated Akt1 in NSCLC cells substantially rescued resveratrol-induced glycolysis suppression. The in vivo data indicated that resveratrol obviously suppressed tumor growth in a xenograft mouse model. Our results suggest targeting HK2 or metabolic enzymes appears to be a new approach for clinical NSCLC prevention or treatment.Entities:
Keywords: Akt; Glycolysis; Hexokinases II; Non-small cell lung cancer; Resveratrol
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Year: 2016 PMID: 27829129 DOI: 10.1016/j.yexcr.2016.11.002
Source DB: PubMed Journal: Exp Cell Res ISSN: 0014-4827 Impact factor: 3.905