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Published on: January 18, 2017
miR-145 overexpression triggers alteration of the whole transcriptome and inhibits breast cancer development
1Department of Laboratory Medicine, Zhongnan Hospital of Wuhan University, Wuhan, 430071, China.
Abstract:
Cumulative evidence has associated microRNA (miRNA) with cancer development, and among those miRNAs, miR-145 has been identified as an anti-oncomiRNA. However, the comprehensive mechanisms of action of miR-145 in breast cancer development have not yet been fully elucidated. Herein, we performed next-generation sequencing to detect the expression profiles of the transcriptome and conducted cellular function experiments after miR-145 overexpression. The results verified the inhibitory effects of miR-145 on breast cancer cell proliferation, colony formation, migration and invasion. Sequencing data revealed that miR-145 triggered the alteration of the whole transcriptome and further led to regulation of the competing endogenous RNA (ceRNA) network. Our study also identified a list of 49 target mRNAs of miR-145 and specific non-coding RNAs, which could be utilized as potential breast cancer biomarkers. This study might serve as a significant platform for further research on miR-145 along with the ceRNA network in breast cancer.
Insights
MicroRNA-145 (miR-145) inhibits breast cancer progression by affecting cell proliferation, migration, and invasion. This study identifies miR-145 targets and potential biomarkers within the competing endogenous RNA network.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- MicroRNAs (miRNAs) play a role in cancer development.
- miR-145 is recognized as an anti-oncomiRNA.
- The precise mechanisms of miR-145 in breast cancer remain incompletely understood.
Purpose of the Study:
- To elucidate the comprehensive mechanisms of miR-145 in breast cancer.
- To investigate the impact of miR-145 overexpression on breast cancer cell functions.
- To identify novel molecular targets and biomarkers associated with miR-145.
Main Methods:
- Next-generation sequencing for transcriptome profiling.
- Cellular function assays (proliferation, colony formation, migration, invasion) following miR-145 overexpression.
- Analysis of the competing endogenous RNA (ceRNA) network.
Main Results:
- miR-145 overexpression significantly inhibited breast cancer cell proliferation, colony formation, migration, and invasion.
- Transcriptome analysis revealed widespread alterations induced by miR-145.
- A list of 49 target messenger RNAs (mRNAs) and specific non-coding RNAs regulated by miR-145 was identified.
- Evidence suggests miR-145 regulates the ceRNA network in breast cancer.
Conclusions:
- miR-145 functions as a tumor suppressor in breast cancer.
- miR-145 influences breast cancer progression through transcriptome modulation and ceRNA network regulation.
- The identified miR-145 targets and non-coding RNAs represent potential biomarkers for breast cancer diagnosis and prognosis.
- This research provides a foundation for further investigation into miR-145 and ceRNA networks in breast cancer.
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