MYH9 is crucial for stem cell-like properties in non-small cell lung cancer by activating mTOR signaling

被引:29
作者
Chen, Meng [1 ]
Sun, Li-Xin [1 ]
Yu, Long [1 ]
Liu, Jun [1 ]
Sun, Li-Chao [1 ]
Yang, Zhi-Hua [1 ]
Shu, Xiong [2 ]
Ran, Yu-Liang [1 ]
机构
[1] Chinese Acad Med Sci & Peking Union Med Coll, Canc Hosp, Natl Clin Res Ctr Canc, State Key Lab Mol Oncol,Natl Canc Ctr, Beijing, Peoples R China
[2] Beijing JiShuiTan Hosp, Beijing Res Inst Orthopaed & Traumatol, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
NONMUSCLE MYOSIN IIA; SIDE POPULATION; TARGETED THERAPY; EXPRESSION; INVASION; IDENTIFICATION; METASTASIS; MIGRATION; MARKER; TUMORS;
D O I
10.1038/s41420-021-00681-z
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The fatality rate of non-small cell lung cancer (NSCLC) has been high due to the existence of cancer stem cells (CSCs). Non-muscle myosin heavy chain 9 (MYH9) can promote the progression of various tumors, but its effect on the stem cell-like characteristics of lung cancer cells (LCCs) has not been clarified. Our research found that the stemness characteristics of LCCs were significantly enhanced by the overexpression of MYH9, and the knockout of MYH9 had the opposite effects. The in vivo with inhibitor blebbistatin further confirmed the effect of MYH9 on the stem cell-like behavior of LCCs. Furthermore, western blotting showed that the expression level of CSCs markers (CD44, SOX2, Nanog, CD133, and OCT4) was also regulated by MYH9. Mechanistic studies have shown that MYH9 regulates stem cell-like features of LCCs by regulating the mTOR signaling pathway, which was supported by sphere formation experiments after LCCs were treated with inhibitors Rapamycin and CHIR-99021. Importantly, high expression of MYH9 in lung cancer is positively correlated with poor clinical prognosis and is an independent risk factor for patients with NSCLC.
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页数:10
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