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An In Vitro Protocol for Evaluating MicroRNA Levels, Functions, and Associated Target Genes in Tumor Cells
Published on: May 21, 2019
lncRNA MRUL Suppressed Non-Small Cell Lung Cancer Cells Proliferation and Invasion by Targeting miR-17-5p/SRSF2 Axis
Ying Chen1, Tianle Shen2, Xuping Ding3
1Department of Radiation Oncology, Zhejiang Key Laboratory of Radiation Oncology, The Cancer Hospital of the University of Chinese Academy of Sciences (Zhejiang Cancer Hospital); Institute of Basic Medicine and Cancer (IBMC), Chinese Academy of Sciences, 1 Banshandong Road, 310022 hangzhou, Zhejiang, China.
Abstract:
The two broad histological subtypes of lung cancer are small cell lung cancer (SCLC) and non-small cell lung cancer (NSCLC), which are the leading causes of cancer-related death in the world. Long noncoding RNAs (lncRNAs) have been verified to be critical in the regulation of cancer development. The present study identified and elucidated the regulatory roles of a novel lncRNA MRUL in NSCLC. The results showed that MRUL was overexpressed in NSCLC samples and correlated with the poor prognosis of patients who had NSCLC. Moreover, this research has for the first time demonstrated that MRUL acted as an oncogenetic lncRNA in NSCLC. Knockdown of MRUL considerably repressed NSCLC cell proliferation, invasion, and migration. The bioinformatics analysis showed that MRUL was involved in regulating multiple RNA splicing and proliferation-related biological processes, such as mRNA splicing, RNA splicing, mRNA processing, mRNA 3'-end processing, mRNA splice site selection, and DNA replication. By combining bioinformatics analysis and experimental validation, we found that MRUL regulated NSCLC progression through promoting SRSF2 by sponging miR-17 in NSCLC cells. The discoveries indicated that MRUL could be a therapeutic target and a potential diagnostic for NSCLC.
Insights
A novel long noncoding RNA, MRUL, is overexpressed in non-small cell lung cancer (NSCLC) and promotes tumor progression. Targeting MRUL could offer new therapeutic and diagnostic strategies for NSCLC patients.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Non-small cell lung cancer (NSCLC) is a leading cause of cancer mortality worldwide.
- Long noncoding RNAs (lncRNAs) play crucial roles in cancer development and progression.
- The specific roles of many lncRNAs in NSCLC remain to be fully elucidated.
Purpose of the Study:
- To identify and characterize a novel lncRNA, MRUL, in the context of non-small cell lung cancer (NSCLC).
- To investigate the regulatory mechanisms and functional significance of MRUL in NSCLC progression.
- To evaluate MRUL as a potential therapeutic target and diagnostic biomarker for NSCLC.
Main Methods:
- Bioinformatic analysis to predict the functions of MRUL.
- Experimental validation including gene knockdown and cell-based assays (proliferation, invasion, migration).
- Investigation of the molecular interaction between MRUL, miR-17, and SRSF2.
Main Results:
- MRUL was found to be significantly overexpressed in NSCLC tissues and associated with poor patient prognosis.
- Knockdown of MRUL suppressed NSCLC cell proliferation, invasion, and migration.
- MRUL promotes NSCLC progression by sponging miR-17, leading to increased SRSF2 expression.
Conclusions:
- MRUL functions as an oncogenic lncRNA in non-small cell lung cancer.
- The MRUL/miR-17/SRSF2 axis represents a novel regulatory pathway in NSCLC.
- MRUL holds potential as a diagnostic biomarker and therapeutic target for NSCLC.
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