| Literature DB >> 33155364 |
Yabo Jiang1, Yongzhen Tao2, Xiuping Zhang3, Xubiao Wei1, Min Li2, Xuxiao He2, Bin Zhou1, Weixing Guo1, Huiyong Yin2, Shuqun Cheng1.
Abstract
Hepatocellular carcinoma (HCC) is one of the most common malignancies worldwide. Here, we identified that increased miR-23a expression in HCC tissues was associated with worse survival. More importantly, we found that STAT5A was a target of miR-23a, whose levels significantly decreased in tumor tissues. Stable expression of STAT5A in Huh7 cells suppressed glucose metabolism and tumor growth. Finally, this study showed that increased miR-23a negatively regulated STAT5A, which further activated AKT signaling to enable rapid metabolism for accelerated tumor growth in HCC. Taken together, our results demonstrated that the miR-23a-STAT5A-AKT signaling pathway is critical to alter glucose metabolism in HCC and may offer new opportunities for effective therapy.Entities:
Keywords: AKT; STAT5A; glucose metabolism; hepatocellular carcinoma; miR-23a; tumor growth
Mesh:
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Year: 2020 PMID: 33155364 PMCID: PMC7858139 DOI: 10.1002/1878-0261.12846
Source DB: PubMed Journal: Mol Oncol ISSN: 1574-7891 Impact factor: 7.449