He Bing, Li Ting, Guan Lei, Liu Fang-E, Chen Xue-Mei, Zhao Jing, Lin Song, Liu Zhi-Zhen, Zhang Hu-Qin
The Key Laboratory of Biomedical Information Engineering of Ministry of Education, School of Life Science and Technology, Xi'an Jiaotong University, Xi'an 710049, P.R. China.
The Center of Basic Medicine Teaching Experiments, School of Basic Medicine, Fourth Military Medicine University (FMMU), Xi'an 710032, P.R. China.
Oncotarget. 2016 Feb 16;7(7):8078-89. doi: 10.18632/oncotarget.6978.
Hepatocellular carcinoma (HCC) is a common and leading cause of death worldwide. Here, we identified that a cell-cell adhesion gene, CTNNA3, is a tumor suppressor in HCC. CTNNA3 inhibited the proliferation, migration and invasion of HCC cell lines. In these cells, CTNNA3 inhibited Akt signal, and in turn decreased the proliferating cell nuclear antigen (PCNA) and the matrix metallopeptidase MMP-9, and increased the cell cycle inhibitor p21(Cip1/Waf1). Meanwhile, CTNNA3 is inhibited by miR-425 in HCC. The miR-425 directly bound to the 3'UTR of CTNNA3 and inhibited its expression. The tumor suppressor function of CTNNA3 and the oncogenic function of miR-425 were further confirmed in HCC cell xenograft in nude mice. The miR-425/CTNNA3 axis may provide insights into the mechanisms underlying HCC, and contribute to potential therapeutic strategy of HCC.
肝细胞癌(HCC)是全球范围内常见且主要的死亡原因。在此,我们发现一种细胞间粘附基因CTNNA3是HCC中的肿瘤抑制因子。CTNNA3抑制HCC细胞系的增殖、迁移和侵袭。在这些细胞中,CTNNA3抑制Akt信号,进而降低增殖细胞核抗原(PCNA)和基质金属蛋白酶MMP-9,并增加细胞周期抑制剂p21(Cip1/Waf1)。同时,CTNNA3在HCC中受到miR-425的抑制。miR-425直接与CTNNA3的3'UTR结合并抑制其表达。CTNNA3的肿瘤抑制功能和miR-425的致癌功能在裸鼠HCC细胞异种移植中得到进一步证实。miR-425/CTNNA3轴可能为HCC的潜在机制提供见解,并有助于HCC的潜在治疗策略。