BMP9 promotes autophagy and inhibits migration and invasion in breast cancer cells through the c-Myc/SNHG3/mTOR signaling axis

被引:5
|
作者
Yu, Huomei [1 ]
Chen, Yuanxiang [1 ]
Lang, Lei [2 ]
Liao, Deyu [1 ]
Liu, Shiyan [1 ]
Yu, Tao [1 ]
Hu, Kai [1 ]
Zhou, Lan [1 ]
Zhang, Yan [1 ]
机构
[1] Chongqing Med Univ, Dept Lab Med, Key Lab Med Diagnost Minist Educ, Chongqing 400016, Peoples R China
[2] Chongqing Univ, Chongqing Univ Cent Hosp, Chongqing Emergency Med Ctr, Sch Med,Dept Clin Lab, Chongqing 400014, Peoples R China
基金
中国国家自然科学基金;
关键词
Breast cancer; BMP9; Long non-coding RNA; Autophagy; Migration; Invasion;
D O I
10.1016/j.tice.2023.102073
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
We previously reported that BMP9 inhibited breast cancer progression. However, the precise molecular mechanism is still unknown. Based on our RNA-sequencing (RNA-seq) results, BMP9 significantly down-regulated the expression of long non-coding RNA SNHG3. Exogenous BMP9 promoted autophagy and inhibited migration and invasion in MDA-MB-231 cells, which was effectively blunted by SNHG3 overexpression. Interestingly, SNHG3 was negatively connected with autophagy. Knockdown of SNHG3 induced autophagy by increasing the formation of autophagic vacuoles and thus inhibited the migration and invasion of MDA-MB-231 cells. Mechanically, BMP9-SNHG3 activated AMPK, AKT and mTOR signaling pathways to induce autophagy and inhibit migration and invasion. Meanwhile, BMP9 regulated SNHG3 transcription by suppressing c-Myc entry into the nucleus. In conclusion, BMP9 promotes autophagy and inhibits migration and invasion in breast cancer cells through the cMyc/SNHG3/mTOR signaling axis, which might offer a fresh perspective on BMP9's breast cancer-inhibiting properties.
引用
收藏
页数:8
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