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MiR-135a-3p inhibits the progression of prostate cancer by targeting TLR4.

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Cancer biology & therapy 📖 저널 OA 98.5% 2023: 1/1 OA 2024: 8/8 OA 2025: 41/41 OA 2026: 13/13 OA 2023~2026 2025 Vol.26(1) p. 2545653
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Li L, Zhang X

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To explore the expression of miR-135a-3p in prostate cancer,analyze its effects on tumor development and the involved mechanisms.

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APA Li L, Zhang X (2025). MiR-135a-3p inhibits the progression of prostate cancer by targeting TLR4.. Cancer biology & therapy, 26(1), 2545653. https://doi.org/10.1080/15384047.2025.2545653
MLA Li L, et al.. "MiR-135a-3p inhibits the progression of prostate cancer by targeting TLR4.." Cancer biology & therapy, vol. 26, no. 1, 2025, pp. 2545653.
PMID 40843910 ↗

Abstract

To explore the expression of miR-135a-3p in prostate cancer,analyze its effects on tumor development and the involved mechanisms. A total of 125 specimens of cancer tissues and corresponding adjacent normal tissues from prostate cancer patients were collected. Real - Time quantitative PCR was employed to quantify the expression levels of miR-135a-3p in prostate cancer tissues and cell lines. Kaplan-Meier survival curve analysis and Cox regression were performed to evaluate the prognostic significance of miR-135a-3p in prostate cancer. The CCK-8 assay was used to detect cell proliferation. A dual-luciferase reporter assay was employed to validate the targeting interaction between miR-135a-3p and Toll-like receptor 4 (TLR4). miR-135a-3p is lowly expressed in prostate cancer tissues and cells, and its low expression is associated with poor prognosis of patients. The low expression state of miR-135a-3p showed a significant correlation with TNM stage, clinical stage, Gleason score, and lymph node metastasis. In addition, miR-135a-3p inhibits the proliferation of prostate cancer cells and cancer progression by negatively regulating the expression of TLR4. miR-135a-3p is downregulated in prostate cancer and is associated with poor prognosis of patients. It exerts an inhibitory effect on the progression of prostate cancer by targeting TLR4.

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