- Author:
Pei QU
1
,
2
;
Zhi Ang SHAO
1
,
2
;
Bing WANG
1
,
2
;
Jin Peng HE
1
,
2
;
Ya Nan ZHANG
3
;
Wen Jun WEI
1
,
2
;
Jun Rui HUA
3
;
Heng ZHOU
1
,
2
;
Dong LU
1
,
2
;
Nan DING
1
,
2
;
Ju Fang WANG
1
,
2
Author Information
- Publication Type:Journal Article
- Keywords: Epithelium-to-mesenchymal transition (EMT); Ionizing Radiation; TGF-β1; miR-663a; microRNA
- MeSH: Down-Regulation; Epithelial-Mesenchymal Transition; Epithelium/metabolism*; MicroRNAs/metabolism*; Transforming Growth Factor beta1/pharmacology*
- From: Biomedical and Environmental Sciences 2022;35(5):437-447
- CountryChina
- Language:English
-
Abstract:
Objective:miR-663a has been reported to be downregulated by X-ray irradiation and participates in radiation-induced bystander effect via TGF-β1. The goal of this study was to explore the role of miR-663a during radiation-induced Epithelium-to-mesenchymal transition (EMT).
Methods:TGF-β1 or IR was used to induce EMT. After miR-663a transfection, cell migration and cell morphological changes were detected and the expression levels of miR-663a, TGF-β1, and EMT-related factors were quantified.
Results:Enhancement of cell migration and promotion of mesenchymal changes induced by either TGF-β1 or radiation were suppressed by miR-663a. Furthermore, both X-ray and carbon ion irradiation resulted in the upregulation of TGF-β1 and downregulation of miR-663a, while the silencing of TGF-β1 by miR-663a reversed the EMT process after radiation.
Conclusion:Our findings demonstrate an EMT-suppressing effect by miR-663a via TGF-β1 in radiation-induced EMT.