Argininosuccinate synthase 1 suppresses cancer cell invasion by inhibiting STAT3 pathway in hepatocellular carcinoma

被引:30
作者
Tao, Xuemei [1 ]
Zuo, Qiaozhu [1 ]
Ruan, Haoyu [1 ]
Wang, Hui [1 ]
Jin, Haojie [1 ]
Cheng, Zhuoan [2 ]
Lv, Yuanyuan [1 ]
Qin, Wenxin [1 ]
Wang, Cun [1 ]
机构
[1] Shanghai Jiao Tong Univ, State Key Lab Oncogenes & Related Genes, Dept Tumor Microenvironm, Shanghai Canc Inst,Renji Hosp,Sch Med, Shanghai 200032, Peoples R China
[2] Shanghai Jiao Tong Univ, Dept Biomed Engn, Shanghai 200240, Peoples R China
基金
中国国家自然科学基金;
关键词
ASS1; hepatocellular carcinoma; prognosis; metastasis; PEGYLATED ARGININE DEIMINASE; IN-VITRO; SYNTHETASE; EXPRESSION; METASTASIS; GROWTH;
D O I
10.1093/abbs/gmz005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Metastasis is the main reason for high recurrence and poor survival of hepatocellular carcinoma (HCC). The molecular mechanism underlying HCC metastasis remains unclear. In this study, we found that argininosuccinate synthase 1 (ASS1) expression was significantly decreased and down-regulation of ASS1 was closely correlated with poor prognosis in HCC patients. DNA methylation led to the down-regulation of ASS1 in HCC. Stable silencing of ASS1 promoted migration and invasion of HCC cells, whereas overexpression of ASS1-inhibited metastasis of HCC cells in vivo and in vitro. We also revealed that ASS1-knockdown increased the phosphorylation level of (S727)STAT3, which contributed to HCC metastasis by up-regulation of inhibitor of differentiation 1 (ID1). These findings indicate that ASS1 inhibits HCC metastasis and may serve as a target for HCC diagnosis and treatment.
引用
收藏
页码:263 / 276
页数:14
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