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Updated: Feb 8, 2026

Detection of Targetable Alterations in Non-small Cell Lung Cancer using Next-generation Sequencing
Published on: October 10, 2025
Absent expression of miR-30a promotes the growth of lung cancer cells by targeting MEF2D
Nianxu Luan1, Yi Wang1, Xuedong Liu1
1Department of Pneumology, Qingdao Municipal Hospital, Qingdao, Shandong 266011, P.R. China.
Abstract:
The microRNA (miR)-30 family has been reported to be aberrantly expressed in several types of cancer. However, its contributions to lung cancer remain to be fully elucidated. Myocyte enhancer factor 2D (MEF2D), an oncogene in liver cancer, has been shown to be aberrantly expressed in lung cancer. In the present study, it was found that MEF2D and miR-30a were inversely correlated in lung cancer samples. Using an online database, it was predicted that miR-30a targeted the 3' untranslated region (UTR) of MEF2D mRNA. The activity of luciferase with MEF2D 3'UTR was suppressed by transfecting cells with miR-30a mimics. The results of western blot analysis showed that the miR-30a mimics also suppressed the MEF2D protein. The miR-30a mimics were able to reduce the growth and colonies of lung cancer cells by suppressing MEF2D. The results of FACS and western blot assays showed that the apoptotic rate was reduced by transfection with the miR-30a mimics. Collectively, the aberrant expression of miR-30a in lung cancer promoted the expression of MEF2D protein. miR-30a inhibited the growth and colony formation of the lung cancer cells by promoting apoptosis.
Insights
MicroRNA (miR)-30a suppresses lung cancer growth by targeting MEF2D. This study reveals miR-30a
Area of Science:
- Oncology
- Molecular Biology
- Gene Regulation
Background:
- Aberrant microRNA (miR) expression is implicated in various cancers.
- The role of the miR-30 family in lung cancer pathogenesis requires further investigation.
- Myocyte enhancer factor 2D (MEF2D) is an oncogene implicated in liver and lung cancers.
Purpose of the Study:
- To elucidate the role of miR-30a in lung cancer.
- To investigate the relationship between miR-30a and MEF2D in lung cancer.
- To determine the functional impact of miR-30a on lung cancer cell behavior.
Main Methods:
- Correlation analysis of MEF2D and miR-30a expression in lung cancer tissues.
- Bioinformatic prediction of miR-30a target sites on MEF2D mRNA.
- Luciferase reporter assays to validate MEF2D 3'UTR targeting by miR-30a.
- Western blot analysis to assess MEF2D protein levels.
- Cell viability, colony formation, and apoptosis assays (FACS) following miR-30a mimic transfection.
Main Results:
- MEF2D and miR-30a expression were inversely correlated in lung cancer samples.
- miR-30a directly targeted the 3' untranslated region (UTR) of MEF2D mRNA.
- Transfection with miR-30a mimics suppressed MEF2D protein expression.
- miR-30a mimics reduced lung cancer cell growth and colony formation.
- miR-30a mimics promoted apoptosis in lung cancer cells.
Conclusions:
- Aberrant expression of miR-30a in lung cancer is associated with increased MEF2D protein levels.
- miR-30a functions as a tumor suppressor in lung cancer by inhibiting MEF2D.
- miR-30a inhibits lung cancer cell proliferation and colony formation by inducing apoptosis.
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