CircRNA circ_POLA2 promotes lung cancer cell stemness via regulating the miR-326/GNB1 axis

被引:48
|
作者
Fan, Zhaohui [1 ,2 ,3 ]
Bai, Yongkang [1 ,2 ,3 ]
Zhang, Qian [1 ,2 ,3 ]
Qian, Pudong [2 ,3 ,4 ]
机构
[1] Nanjing Med Univ, Jiangsu Canc Hosp, Dept Thorac Surg, Nanjing, Peoples R China
[2] Nanjing Med Univ, Jiangsu Inst Canc Res, Baiziting 42, Nanjing 210009, Jiangsu, Peoples R China
[3] Nanjing Med Univ, Affiliated Canc Hosp, Baiziting 42, Nanjing 210009, Jiangsu, Peoples R China
[4] Nanjing Med Univ, Jiangsu Canc Hosp, Dept Radiotherapy, Baiziting 42, Nanjing 210009, Jiangsu, Peoples R China
关键词
circ_POLA2; circRNA; GNB1; lung cancer; miR-326; stemness; PROLIFERATION; EXPRESSION; PROGRESSION; METASTASIS; LEUKEMIA; GNB1;
D O I
10.1002/tox.22980
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Circular RNAs (CircRNAs) are a group of noncoding RNAs that have essential function in the development and progression of various cancers. The expression pattern and function of circRNA in lung cancer is not fully understood. In the present study, we aimed to investigate the expression profiles and underlying mechanism of circRNA circ_POLA2 in lung cancer cell stemness. Circ_POLA2 was highly expressed in lung cancer tissues and predicted a poor prognosis in lung cancer patients. Knockdown of circ_POLA2 inhibited the stemness of lung cancer cells, which is evident by the decreased sphere-formation ability, ALDH1 activity, and stemness marker expression, but had no effects on cell viability. Mechanistically, circ_POLA2 functioned as a ceRNA by sponging miR-326. Furthermore, miR-326 negatively regulated G protein subunit beta 1 (GNB1) expression by targeting its 3 '-UTR (untranslated region). Intriguingly, we found that GNB1 was overexpressed and associated with poor prognosis in lung cancer patients. Overexpression of GNB1 could antagonize the inhibitory effect of circ_POLA2 knockdown on lung cancer cell stemness. In conclusion, circ_POLA2 promotes lung cancer cell stemness and progression via regulating the miR-326/GNB1 axis, which might serve as a novel therapeutic target for lung cancer patients.
引用
收藏
页码:1146 / 1156
页数:11
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