The Key microRNAs Regulated the Development of Non-small Cell Lung Cancer by Targeting TGF-β-induced epithelial-mesenchymal Transition
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Updated: Jan 26, 2026

Studying TGF-β Signaling and TGF-β-induced Epithelial-to-mesenchymal Transition in Breast Cancer and Normal Cells
Published on: October 27, 2020
Purpose:
Epithelial-to-Mesenchymal Transition (EMT) was reported to play a key role in the development of Non-Small Cell Lung Cancer (NSCLC). The process of EMT is regulated by the changes of miRNAs expression. However, it is still unknown which miRNA changed the most in the process of canceration and whether these changes played a role in tumor development.
Methods:
A total of 36 SCLC patients treated in our hospital between 11th, 2015 and 10th, 2017 were enrolled. The samples of cancer tissues and paracancer tissues of patients were collected and analyzed. Then, the miRNAs in normal lung cells and NSCLC cells were also analyzed. In the presence of TGF-β, we transfected the miRNA mimics or inhibitor into NSCLC cells to investigate the role of the significantly altered miRNAs in cell migration and invasion and in the process of EMT.
Results:
MiR-330-3p was significantly up-regulated in NSCLC cell lines and tissues and miRNA- 205 was significantly down-regulated in NSCLC cell lines and NSCLC tissues. Transfected miRNA-205 mimics or miRMA-330-3p inhibitor inhibited the migration and invasion of NCIH1975 cell and restrained TGF-β-induced EMT in NSCLC cells.
Conclusion:
miRNA-330-3p and miRNA-205 changed the most in the process of canceration in NSCLC. Furthermore, miR-330-3p promoted cell invasion and metastasis in NSCLC probably by promoting EMT and miR-205 could restrain NSCLC likely by suppressing EMT.
Insights
MicroRNA-330-3p and microRNA-205 are key players in Non-Small Cell Lung Cancer (NSCLC) development. Upregulated miR-330-3p promotes metastasis by enhancing EMT, while downregulated miR-205 restrains NSCLC by suppressing EMT.
Area of Science:
- Oncology
- Molecular Biology
- Gene Regulation
Background:
- Epithelial-to-Mesenchymal Transition (EMT) is crucial in Non-Small Cell Lung Cancer (NSCLC) development.
- MicroRNA (miRNA) expression changes regulate EMT, but specific key miRNAs in NSCLC canceration remain unclear.
Purpose of the Study:
- Identify the most significantly altered miRNAs during NSCLC canceration.
- Investigate the role of these miRNAs in tumor development and EMT.
Main Methods:
- Analyzed miRNA expression in NSCLC tissues and cell lines.
- Utilized miRNA mimics and inhibitors in NSCLC cells with TGF-β stimulation.
- Assessed effects on cell migration, invasion, and EMT.
Main Results:
- MiR-330-3p was significantly upregulated, and miR-205 was significantly downregulated in NSCLC.
- Inhibition of miR-330-3p and restoration of miR-205 reduced NCIH1975 cell migration and invasion.
- These miRNAs modulated TGF-β-induced EMT in NSCLC cells.
Conclusions:
- MiR-330-3p and miR-205 exhibit the most significant changes during NSCLC canceration.
- MiR-330-3p promotes NSCLC invasion and metastasis via EMT.
- MiR-205 suppresses NSCLC progression by inhibiting EMT.
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