The METTL3/miR-196a Axis Predicts Poor Prognosis in Non-small Cell Lung Cancer
- Zhen Yang 1,2, Jie Hao 3, Minghan Qiu 2,4, Ruxue Liu 2,4, Hanwei Mei 2,4, Qiaonan Zhang 3, Zhanhua Gao 3, Wenwen Pang 1, Jing Liu 1, Wenjie Pan 1, Huaqing Wang 2,4, Ming Gao 3
- Zhen Yang 1,2, Jie Hao 3, Minghan Qiu 2,4
- 1Department of Clinical Laboratory, Tianjin Union Medical Center of Nankai University, Tianjin 300121, China.
- 2The Institute of Translational Medicine, Tianjin Union Medical Center of Nankai University, Tianjin 300121, China.
- 3Department of Thyroid and Breast Surgery, Tianjin Key Laboratory of General Surgery in Construction, Tianjin Union Medical Center of Nankai University, Tianjin 300121, China.
- 4Department of Oncology, Tianjin Union Medical Center of Nankai University, Tianjin 300121, China.
- 0Department of Clinical Laboratory, Tianjin Union Medical Center of Nankai University, Tianjin 300121, China.
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View abstract on PubMed
Summary
This summary is machine-generated.METTL3 upregulation promotes non-small cell lung cancer (NSCLC) progression via the METTL3-miR-196a-GAS7 axis. This pathway influences tumor growth and may serve as a novel diagnostic and therapeutic target for NSCLC.
Area Of Science
- Molecular Oncology
- Cancer Biology
- Epigenetics
Background
- METTL3, an m6A methyltransferase, is implicated in cancer progression, including non-small cell lung cancer (NSCLC).
- Understanding the role of METTL3-mediated upregulation of microRNA-196a (miR-196a) in NSCLC is crucial.
Purpose Of The Study
- To elucidate the function and mechanism of METTL3-driven miR-196a upregulation in NSCLC.
- To investigate the potential of the METTL3-miR-196a-GAS7 axis as a therapeutic target and diagnostic marker for NSCLC.
Main Methods
- Quantitative PCR, Western blot, and immunohistochemistry to assess m6A modification levels.
- Bioinformatic analysis using TCGA, GEPIA, CPTAC, and TIMER databases for gene expression.
- In vitro (cell lines) and in vivo (tumor growth models) experiments to evaluate miR-196a function.
- Interaction analysis between miR-196a and GAS7.
Main Results
- METTL3 and miR-196a were significantly upregulated in NSCLC tissues and correlated with advanced TNM stage, tumor size, metastasis, and poor prognosis.
- Overexpression of miR-196a enhanced NSCLC cell viability and autophagy, while knockdown had opposite effects.
- miR-196a directly interacted with GAS7, and GAS7 expression correlated with immune cell infiltration in the tumor microenvironment.
Conclusions
- The METTL3-miR-196a-GAS7 axis plays a critical role in NSCLC progression.
- This axis represents a promising target for molecular therapy and a potential diagnostic biomarker for NSCLC.
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