| Literature DB >> 35670956 |
Pingshan Yang1, Dongdong Zhang1, Fengli Zhou2, Wenyou Chen1, Chuang Hu1, Duqing Xiao1, Songwang Cai3.
Abstract
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.Entities:
Keywords: DNA methyltransferase 3B; Methylation; Non-small cell lung cancer; microRNA-203a-3p
Mesh:
Substances:
Year: 2022 PMID: 35670956 DOI: 10.1007/s13577-022-00728-y
Source DB: PubMed Journal: Hum Cell ISSN: 0914-7470 Impact factor: 4.174