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Microarray Profiling of TGF-β1-Induced Long Non-Coding RNA Expression Patterns in Human Lung Bronchial Epithelial
Wentao Hu1,2, Weiwei Pei1,2, Lin Zhu1,2
1School of Radiation Medicine and Protection, Medical College of Soochow University, Suzhou, China.
Long non-coding RNAs (lncRNAs) regulated by TGF-β1 are implicated in radiation-induced bystander effects and tumorigenesis. These lncRNAs offer new insights into cancer development following radiation exposure.
Area of Science:
- Molecular Biology
- Cancer Research
- Radiation Biology
Background:
- Transforming growth factor-beta 1 (TGF-β1) mediates radiation-induced bystander effects (RIBE), contributing to malignant transformation and tumorigenesis.
- The precise molecular mechanisms underlying TGF-β1's role in RIBE and subsequent tumorigenesis remain incompletely understood.
Purpose of the Study:
- To identify novel regulatory molecules involved in TGF-β1-mediated RIBE.
- To elucidate the functional roles of differentially expressed long non-coding RNAs (lncRNAs) in this process.
Main Methods:
- lncRNA microarray profiling of human lung bronchial epithelial cells (BEAS-2B) treated with TGF-β1.
- Gene Ontology (GO) and KEGG pathway analyses to predict functions of differentially expressed lncRNAs.
- Quantitative real-time PCR (qRT-PCR) and CCK-8 assays for validation and functional assessment.
Main Results:
- A total of 224 dysregulated lncRNAs were identified, with 6 validated by qRT-PCR.
- Pathway analyses indicated correlations between dysregulated lncRNAs and cell proliferation, transformation, and migration.
- lnc-THEMIS-2 and lnc-ITGB6-4 were found to mitigate TGF-β1-induced decreases in cell viability.
Conclusions:
- TGF-β1-induced lncRNAs play significant roles in oncogenic transformation and tumorigenesis.
- These findings enhance the understanding of mechanisms linking low-dose/low-dose-rate radiation to tumorigenesis via RIBE.
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