Long noncoding RNA MEG3 suppresses liver cancer cells growth through inhibiting β-catenin by activating PKM2 and inactivating PTEN

被引:94
作者
Zheng, Qidi [1 ]
Lin, Zhuojia [1 ]
Xu, Jie [1 ]
Lu, Yanan [1 ]
Meng, Qiuyu [1 ]
Wang, Chen [1 ]
Yang, Yuxin [1 ]
Xin, Xiaoru [1 ]
Li, Xiaonan [1 ]
Pu, Hu [1 ]
Gui, Xin [1 ]
Li, Tianming [1 ]
Xiong, Wujun [2 ]
Lu, Dongdong [1 ]
机构
[1] Tongji Univ, Shanghai East Hosp, Sch Life Sci & Technol, Res Ctr Translat Med, Shanghai 200092, Peoples R China
[2] Tongji Univ, Shanghai East Hosp, Dept Hepatol, Sch Med, Shanghai 200120, Peoples R China
来源
CELL DEATH & DISEASE | 2018年 / 9卷
关键词
UP-REGULATION; HEPATOCELLULAR-CARCINOMA; DECREASED EXPRESSION; STEM-CELLS; PROMOTES; PROLIFERATION; TUMOR; APOPTOSIS; DIFFERENTIATION; MICRORNA-122;
D O I
10.1038/s41419-018-0305-7
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Maternally expressed gene 3 (MEG3) encodes an lncRNA which is suggested to function as a tumor suppressor and has been showed to involve in a variety of cancers. Herein, our findings demonstrate that MEG3 inhibits the malignant progression of liver cancer cells in vitro and in vivo. Mechanistically, MEG3 promotes the expression and maturition of miR122 which targets PKM2. Therefore, MEG3 decreases the expression and nuclear location of PKM2 dependent on miR122. Furthermore, MEG3 also inhibits CyclinD1 and C-Myc via PKM2 in liver cancer cells. On the other hand, MEG3 promotes beta-catenin degradation through ubiquitin-proteasome system dependent on PTEN. Strikingly, MEG3 inhibits beta-catenin activity through PKM2 reduction and PTEN increase. Significantly, we also found that excessive beta-catenin abrogated the effect of MEG3 in liver cancer. In conclusion, our study for the first time demonstrates that MEG3 acts as a tumor suppressor by negatively regulating the activity of the PKM2 and beta-catenin signaling pathway in hepatocarcinogenesis and could provide potential therapeutic targets for the treatment of liver cancer.
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页数:18
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