A c-Myc-MicroRNA functional feedback loop affects hepatocarcinogenesis

被引:82
作者
Han, Han [1 ]
Sun, Dan [1 ]
Li, Wenjuan [1 ]
Shen, Hongxing [1 ]
Zhu, Yahui [1 ]
Li, Chen [1 ]
Chen, Yuxing [1 ]
Lu, Longfeng [1 ]
Li, Wenhua [1 ]
Zhang, Jinxiang [2 ]
Tian, Yuan [1 ]
Li, Youjun [1 ]
机构
[1] Wuhan Univ, Coll Life Sci, State Key Lab Virol, Wuhan 430072, Peoples R China
[2] Huazhong Univ Sci & Technol, Wuhan Union Hosp, Dept Surg, Wuhan 430022, Peoples R China
基金
中国国家自然科学基金;
关键词
GENOMIC INSTABILITY; EXPRESSION; TARGETS; PATHOGENESIS; PROGRESSION; REPRESSION; SIGNATURE; REVEALS; GROWTH; USP28;
D O I
10.1002/hep.26302
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
c-Myc (Myc) plays an important role in normal liver development and tumorigenesis. We show here that Myc is pathologically activated in and essential for promoting human hepatocellular carcinoma (HCC). Myc induces HCC through a novel, microRNA (miRNA)-mediated feedback loop comprised of miR-148a-5p, miR-363-3p, and ubiquitin-specific protease 28 (USP28). Myc directly binds to conserved regions in the promoters of the two miRNAs and represses their expression. miR-148a-5p directly targets and inhibits Myc, whereas miR-363-3p destabilizes Myc by directly targeting and inhibiting USP28. Inhibition of miR-148a-5p or miR-363-3p induces hepatocellular tumorigenesis by promoting G1 to S phase progression, whereas activation of them has the opposite effects. The Myc-miRNA feedback loop is dysregulated in human HCC. Conclusion: These results define miR-148a-5p and miR-363-3p as negative regulators of Myc, thus revealing their heretofore unappreciated roles in hepatocarcinogenesis. (HEPATOLOGY 2013;57:2378-2389)
引用
收藏
页码:2378 / 2389
页数:12
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