RETRACTED: MicroRNA-449 suppresses proliferation of hepatoma cell lines through blockade lipid metabolic pathway related to SIRT1 (Retracted article. See vol. 63, 2023)

被引:53
作者
Zhang, Hongyi [1 ]
Feng, Zhiqiang [1 ]
Huang, Rui [2 ,3 ]
Xia, Zhengun [2 ,3 ]
Xiang, Guoan [3 ]
Zhang, Jinqian [2 ]
机构
[1] Air Force Gen Hosp, Dept Hepatobiliary Surg, Beijing 100142, Peoples R China
[2] Capital Med Univ, Beijing Ditan Hosp, Inst Infect Dis, Beijing 100015, Peoples R China
[3] Southern Med Univ, Peoples Hosp Guangdong Prov 2, Dept Gen Surg, Guangzhou 510515, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
microRNA; SIRT1; proliferation; SREBP-1c; lipid metabolism; hepatocellular carcinoma; FATTY-ACID SYNTHASE; HEPATOCELLULAR-CARCINOMA; PROSTATE-CANCER; GENE-EXPRESSION; POOR-PROGNOSIS; SREBP-1C; LET-7; TUMORIGENESIS; TRANSCRIPTION; LIPOGENESIS;
D O I
10.3892/ijo.2014.2596
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
MicroRNA (miRNA or miR) inhibition of oncogenic related pathways has been shown to be a promising therapeutic approach for cancer. SIRT1 might be a promoter factor on tumorigenesis of hepatocellular carcinoma (HCC). However, the mechanism is unknown. We investigated whether miRNAs regulate the SIRT1 and its downstream SREBP-lipogenesis-cholesterogenesis metabolic pathway in hepatoma cells. Human hepatoma cells were transfected with miR-449 mimics and inhibitors, and the effects of miR-449 on cell proliferation was assessed. We identified the miRNAs, miR-449, that control lipogenesis and cholesterogenesis in hepatoma cells by inhibiting SIRT1 and SREBP-1c expression and downregulating their targeted genes, including fatty acid synthase (FASN) and 3-hydroxy-3-methylglutaryl CoA reductase (HMGCR). MiR-449 repressed DNA synthesis, mitotic entry and proliferation of hepatoma cells. Restoration of miR-449 led to suppression of SIRT1 expression and liver tumorigenesis. The newly identified miRNAs, miR-449 represents a novel targeting mechanism for HCC therapy.
引用
收藏
页码:2143 / 2152
页数:10
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