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Ectopic expressed miR-203 contributes to chronic obstructive pulmonary disease via targeting TAK1 and PIK3CA
Liang Shi1, Qinghong Xin2, Ruonan Chai3
1Department of Respiratory Disease, Chinese PLA General Hospital Beijing 100853, China.
Abstract:
MiRNA is a group of powerful short non-coding RNAs that suppress the expression of protein coding genes by targeting to the 3'UTRs of mRNAs. Some researchers have detected the miRNAs expression profile in tissue and blood samples of chronic obstructive pulmonary disease (COPD) patients recently. Several disturbed miRNAs were found to be related to COPD; however, the mechanisms were still well understood. In this study, we first detected the expression of 11 candidate miRNAs in the lung samples of COPD patients, non-COPD smokers and non-smock controls. We found that the expression of miR-181a, miR-203, miR-338, miR-1 and miR-199a was altered compared with control. Subsequently, we detected these five miRNAs expression in the blood samples of the participants. A significant higher expression of miR-203 was found in the blood samples of smokers and COPD patients. Predicted by bioinformatics tools and confirmed by luciferase assay and western blot, we demonstrated that TAK1 and PIK3CA are two direct targets of miR-203. Furthermore, we detected a lower p-IκBα and p-p65 level in the bronchial/tracheal epithelial cells from COPD patients compared with the cells from healthy controls, when stimulated by LPS. The concentration of TNF-α and IL-6 in the medium from bronchial/tracheal epithelial cells from COPD patients is also lower. Meanwhile, the miR-203 level was down-regulated significantly in the control cells, but non-significant change in the cells from COPD patients. miR-203 represses NF-κB signaling via targeting TAK1 and PI3KCA and miR-203 overexpression may contribute to the COPD initiation.
Insights
MicroRNAs (miRNAs) play a role in chronic obstructive pulmonary disease (COPD). This study found miR-203 targets TAK1 and PIK3CA, suggesting its role in COPD pathogenesis.
Area of Science:
- Molecular Biology
- Genetics
- Pulmonology
Background:
- MicroRNAs (miRNAs) are short non-coding RNAs regulating gene expression.
- Altered miRNA profiles are observed in chronic obstructive pulmonary disease (COPD) patients.
- The precise mechanisms of miRNA involvement in COPD remain unclear.
Purpose of the Study:
- Investigate miRNA expression in COPD lung and blood samples.
- Identify specific miRNAs and their targets involved in COPD.
- Elucidate the role of miR-203 in regulating inflammatory pathways in COPD.
Main Methods:
- miRNA expression profiling in lung and blood samples from COPD patients, smokers, and controls.
- Bioinformatic prediction, luciferase assays, and Western blot to identify miRNA targets.
- Analysis of NF-κB signaling pathway components (p-IκBα, p-p65) and inflammatory cytokines (TNF-α, IL-6) in epithelial cells.
Main Results:
- Expression of miR-181a, miR-203, miR-338, miR-1, and miR-199a was altered in COPD lung samples.
- miR-203 expression was significantly higher in blood of smokers and COPD patients.
- TAK1 and PIK3CA were confirmed as direct targets of miR-203.
- COPD epithelial cells showed lower p-IκBα and p-p65 levels upon LPS stimulation.
- miR-203 overexpression in control cells repressed NF-κB signaling.
Conclusions:
- miR-203 directly targets TAK1 and PIK3CA, key regulators of the NF-κB pathway.
- Downregulation of miR-203 may contribute to COPD pathogenesis by promoting inflammation.
- miR-203 represents a potential therapeutic target for COPD.
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