LncRNA SNHG3 promotes gastric cancer cell proliferation and metastasis by regulating the miR-139-5p/MYB axis

被引:0
|
作者
Xie, Yan [1 ,2 ]
Rong, Li [3 ]
He, Min [1 ]
Jiang, Yuyou [1 ]
Li, Haiyu [4 ]
Mai, Li [5 ]
Song, Fangzhou [1 ]
机构
[1] Chongqing Med Univ, Mol Med & Canc Res Ctr, Chongqing 400016, Peoples R China
[2] Chongqing Med Univ, Qinggang Senior Care Ctr, Affiliated Hosp 1, Chongqing 400016, Peoples R China
[3] Bishan Hosp Chongqing, Dept Gastroenterol, Chongqing 402760, Peoples R China
[4] Chongqing Publ Hlth Med Ctr, Chongqing 400036, Peoples R China
[5] Chongqing Med Univ, Dept Lab Med, Affiliated Hosp 2, Chongqing 400010, Peoples R China
来源
AGING-US | 2021年 / 13卷 / 23期
基金
中国国家自然科学基金;
关键词
gastric cancer; SNHG3; miR-139-5p; MYB;
D O I
暂无
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The long non-coding RNA (lncRNA) SNHG3 has been shown to play oncogenic roles in several cancer types, but the mechanisms underlying its activity are poorly understood. In this study, we aimed to explore the clinical relevance and mechanistic role of SNHG3 in gastric cancer (GC). We found that SNHG3 expression in GC cell lines and tissues was significantly increased, and the upregulation of this lncRNA was correlated with tumor clinical stage and decreased patient survival. Knocking down SNHG3 in GC cells impaired the proliferative, migratory, and invasive activity in vitro and constrained in vivo GC xenograft tumor growth. Mechanistically, SNHG3 was found to bind and sequester miR-139-5p, thereby indirectly promoting the upregulation of the miR139-5p target gene MYB. These data demonstrated that SNHG3 functions in an oncogenic manner to drive GC proliferation, migration, and invasion by regulating the miR-139-5p/MYB axis.
引用
收藏
页码:25138 / 25152
页数:15
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