| Literature DB >> 28325773 |
Xiuying Zhong1, Shengya Tian1, Xiang Zhang1, Xinwei Diao2, Fangting Dong2, Jie Yang2, Zhaoyong Li1, Linchong Sun1, Lin Wang1, Xiaoping He1, Gongwei Wu1, Xin Hu1, Lihua Wang1, Libing Song3, Huafeng Zhang1, Xin Pan2, Ailing Li4, Ping Gao5.
Abstract
Cancer progression depends on cellular metabolic reprogramming as both direct and indirect consequence of oncogenic lesions; however, the underlying mechanisms are still poorly understood. Here, we report that CUEDC2 (CUE domain-containing protein 2) plays a vital role in facilitating aerobic glycolysis, or Warburg effect, in cancer cells. Mechanistically, we show that CUEDC2 upregulates the two key glycolytic proteins GLUT3 and LDHA via interacting with the glucocorticoid receptor (GR) or 14-3-3ζ, respectively. We further demonstrate that enhanced aerobic glycolysis is essential for the role of CUEDC2 to drive cancer progression. Moreover, using tissue microarray analysis, we show a correlation between the aberrant expression of CUEDC2, and GLUT3 and LDHA in clinical HCC samples, further demonstrating a link between CUEDC2 and the Warburg effect during cancer development. Taken together, our findings reveal a previously unappreciated function of CUEDC2 in cancer cell metabolism and tumorigenesis, illustrating how close oncogenic lesions are intertwined with metabolic alterations promoting cancer progression.Entities:
Keywords: zzm321990LDHAzzm321990; CUEDC2; GLUT3; Warburg effect; tumorigenesis
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Year: 2017 PMID: 28325773 PMCID: PMC5412808 DOI: 10.15252/embr.201643617
Source DB: PubMed Journal: EMBO Rep ISSN: 1469-221X Impact factor: 8.807