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Updated: Jan 24, 2026

Detection of Targetable Alterations in Non-small Cell Lung Cancer using Next-generation Sequencing
Published on: October 10, 2025
Altered expression of microRNA-365 is related to the occurrence and development of non-small-cell lung cancer by
Qian Han1, Peng Cheng1, Hongjie Yang1
1Department of Radiotherapy, Henan Provincial People's Hospital, Zhengzhou, Henan, People's Republic of China.
Abstract:
The purpose of this current study is to elucidate whether altered microRNA-365 (miR-365) has an association with the initiation and development of non-small-cell lung cancer (NSCLC) by targeting TRIM25 expression. The expression of miR-365 and TRIM25 in NSCLC tissues, adjacent normal tissues, and NSCLC cell lines were detected. The relationship between miR-365 expression and TRIM25 with the clinicopathological characteristics of NSCLC was analyzed. The putative binding site between miR-365 and TRIM25 was determined by luciferase activity assay. miR-365 inhibitors and miR-365 mimics were transfected to human NSCLC A549 cells, and the cell viability was detected by cell counting kit-8 assay; flow cytometry was carried out to determine cell cycle and apoptosis rate. Poorly expressed miR-365 and overexpressed TRIM25 was found in NSCLC tissues. TRIM25 was determined as a target gene of miR-365. The miR-365 and TRIM25 expression were related to the clinicopathological features of NSCLC, such as pathological classification, differentiation degree, TNM stage as well as lymph node metastasis. miR-365 suppressed the expression of TRIM25 and elevated the expression of the proapoptotic protein in NSCLC cells. Our study demonstrates that altered expression of miR-365 has a close association with the occurrence and development of NSCLC by inhibiting TRIM25 expression.
Insights
Altered microRNA-365 (miR-365) expression is linked to non-small-cell lung cancer (NSCLC) development. This study shows miR-365 inhibits TRIM25, impacting NSCLC progression and potentially offering new therapeutic targets.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Non-small-cell lung cancer (NSCLC) remains a leading cause of cancer mortality globally.
- MicroRNAs (miRNAs) play crucial roles in cancer development and progression.
- Dysregulation of specific miRNAs, including miR-365, has been implicated in various cancers.
Purpose of the Study:
- To investigate the association between altered microRNA-365 (miR-365) expression and the initiation/development of non-small-cell lung cancer (NSCLC).
- To determine if miR-365 targets TRIM25 expression in NSCLC.
- To explore the functional impact of miR-365 on NSCLC cell behavior.
Main Methods:
- Expression analysis of miR-365 and TRIM25 in NSCLC tissues and cell lines.
- Correlation analysis between miR-365/TRIM25 expression and NSCLC clinicopathological features.
- Luciferase activity assay to confirm direct targeting of TRIM25 by miR-365.
- In vitro functional assays (cell viability, cell cycle, apoptosis) using miR-365 mimics and inhibitors in NSCLC cells.
Main Results:
- Downregulation of miR-365 and upregulation of TRIM25 were observed in NSCLC tissues.
- TRIM25 was confirmed as a direct target gene of miR-365.
- miR-365 and TRIM25 expression levels correlated significantly with NSCLC pathological classification, differentiation, TNM stage, and lymph node metastasis.
- miR-365 mimics suppressed NSCLC cell viability and proliferation, induced apoptosis, and inhibited TRIM25 expression.
Conclusions:
- Altered miR-365 expression is closely associated with the occurrence and development of NSCLC.
- miR-365 exerts its tumor-suppressive effects in NSCLC by inhibiting TRIM25 expression.
- Targeting the miR-365/TRIM25 axis presents a potential therapeutic strategy for NSCLC.
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