Your browser doesn't support javascript.
loading
Erianin promotes apoptosis and inhibits Akt-mediated aerobic glycolysis of cancer cells.
Han, Shuangze; Chen, Sijin; Wang, Jidong; Huang, Sheng; Xiao, Yeqing; Deng, Gaoyan.
Affiliation
  • Han S; Department of Ultrasound, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China.
  • Chen S; Department of Urology, Hunan Provincial People's Hospital, The First Affiliated Hospital of Hunan Normal University, Changsha 410005, Hunan, China.
  • Wang J; Department of Oral and Maxillofacial Surgery, Changde Hospital, Xiangya School of Medicine, Central South University (The first people's hospital of Changde city), Changde 415000, Hunan, China.
  • Huang S; Department of General, Hunan Chest Hospital, Changsha 410013, Hunan, China.
  • Xiao Y; Department of Ultrasonography, Hunan Chest Hospital, Changsha 410013, Hunan, China.
  • Deng G; Department of Thoracic Surgery, Hunan Chest Hospital, Changsha 410013, Hunan, China.
J Cancer ; 15(8): 2380-2390, 2024.
Article in En | MEDLINE | ID: mdl-38495480
ABSTRACT
Highly activated aerobic glycolysis provides the metabolic requirements for tumor cell growth and proliferation. Erianin, a natural product isolated from Dendrobium chrysotoxum Lindl, has been reported to exert antitumor activity in multiple cancers. However, whether Erianin exerts inhibitory effects on aerobic glycolysis and the inherent mechanism remain poorly defined in non-small cell lung cancer (NSCLC). Here, we showed that Erianin inhibited the cell viability and proliferation, and induced apoptosis in NSCLC cells. Moreover, Erianin overtly suppressed aerobic glycolysis via decreasing HK2 expression. Mechanistically, Erianin dose-dependently curbed the Akt-GSK3ß signaling pathway phosphorylation activation, which afterwards downregulated HK2 expression. Meanwhile, Erianin inhibited HCC827 tumor growth in vivo. Taken together, our results suggest that the natural product Erianin can suppress aerobic glycolysis and exert potent anticancer effects via the Akt-GSK3ß signaling pathway in NSCLC cells.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Cancer Year: 2024 Document type: Article Affiliation country: China Country of publication: Australia

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Cancer Year: 2024 Document type: Article Affiliation country: China Country of publication: Australia