miR-203a-3p-DNMT3B feedback loop facilitates non-small cell lung cancer progression

被引:10
作者
Yang, Pingshan [1 ]
Zhang, Dongdong [1 ]
Zhou, Fengli [2 ]
Chen, Wenyou [1 ]
Hu, Chuang [1 ]
Xiao, Duqing [1 ]
Cai, Songwang [1 ]
机构
[1] Jinan Univ, Dept Thorac Surg, Affiliated Hosp 1, Guangzhou 510632, Guangdong, Peoples R China
[2] Sun Yat Sen Univ, Affiliated Hosp 3, Dept Gen Practice, Guangzhou 510630, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
microRNA-203a-3p; DNA methyltransferase 3B; Non-small cell lung cancer; Methylation; DNA METHYLTRANSFERASE 3B; TRANSCRIPTION REPRESSION; MICRORNA THERAPEUTICS; DOWN-REGULATION; DNMT3B; METHYLATION; EXPRESSION; OVEREXPRESSION; MIGRATION; MIR-203;
D O I
10.1007/s13577-022-00728-y
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
It has been reported that microRNA-203a-3p (miR-203a-3p) modulates cell proliferation, migration and invasion in a variety of cancer cell types. However, little is known about its role in lung cancer progression. The present study found that miR-203a-3p was downregulated in non-small cell lung cancer (NSCLC) cell lines and tissues. Overexpression of miR-203a-3p inhibits NSCLC cell proliferation, migration and invasion, and promotes cellular apoptosis in vitro. Restoration of miR-203a-3p expression in A549 and NCI-H520 cells enhances their chemosensitivity. Further experiments showed that DNA methyltransferase 3B (DNMT3B) was a direct target of miR-203a-3p. In addition, the present results revealed that promoter hypermethylation was the potential mechanism responsible for low miR-203a-3p expression in NSCLC. Notably, feedback regulation between miR-203a-3p and DNMT3B was observed in NSCLC. Moreover, Overexpression of miR-203a-3p reduces tumor growth in vivo. In summary, the present study has identified an miR-203a-3p-DNMT3B feedback loop that facilitates NSCLC progression.
引用
收藏
页码:1219 / 1233
页数:15
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