MiR-135a-3p通过靶向TLR4抑制前列腺癌的进展。

IF 4.6 4区 医学 Q2 ONCOLOGY
Cancer Biology & Therapy Pub Date : 2025-12-01 Epub Date: 2025-08-22 DOI:10.1080/15384047.2025.2545653
LianQiang Li, Xiao Zhang
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引用次数: 0

摘要

探讨miR-135a-3p在前列腺癌中的表达,分析其对肿瘤发生发展的影响及其机制。共收集前列腺癌患者癌组织及相应癌旁正常组织125例。Real - Time定量PCR检测miR-135a-3p在前列腺癌组织和细胞系中的表达水平。采用Kaplan-Meier生存曲线分析和Cox回归评价miR-135a-3p在前列腺癌中的预后意义。CCK-8法检测细胞增殖。采用双荧光素酶报告试验验证miR-135a-3p与toll样受体4 (TLR4)之间的靶向相互作用。miR-135a-3p在前列腺癌组织和细胞中低表达,其低表达与患者预后不良有关。miR-135a-3p的低表达状态与TNM分期、临床分期、Gleason评分、淋巴结转移有显著相关性。此外,miR-135a-3p通过负调控TLR4的表达抑制前列腺癌细胞的增殖和癌症的进展。miR-135a-3p在前列腺癌中下调,与患者预后不良相关。它通过靶向TLR4对前列腺癌的进展有抑制作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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

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

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

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

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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来源期刊
Cancer Biology & Therapy
Cancer Biology & Therapy 医学-肿瘤学
CiteScore
7.00
自引率
0.00%
发文量
60
审稿时长
2.3 months
期刊介绍: Cancer, the second leading cause of death, is a heterogenous group of over 100 diseases. Cancer is characterized by disordered and deregulated cellular and stromal proliferation accompanied by reduced cell death with the ability to survive under stresses of nutrient and growth factor deprivation, hypoxia, and loss of cell-to-cell contacts. At the molecular level, cancer is a genetic disease that develops due to the accumulation of mutations over time in somatic cells. The phenotype includes genomic instability and chromosomal aneuploidy that allows for acceleration of genetic change. Malignant transformation and tumor progression of any cell requires immortalization, loss of checkpoint control, deregulation of growth, and survival. A tremendous amount has been learned about the numerous cellular and molecular genetic changes and the host-tumor interactions that accompany tumor development and progression. It is the goal of the field of Molecular Oncology to use this knowledge to understand cancer pathogenesis and drug action, as well as to develop more effective diagnostic and therapeutic strategies for cancer. This includes preventative strategies as well as approaches to treat metastases. With the availability of the human genome sequence and genomic and proteomic approaches, a wealth of tools and resources are generating even more information. The challenge will be to make biological sense out of the information, to develop appropriate models and hypotheses and to translate information for the clinicians and the benefit of their patients. Cancer Biology & Therapy aims to publish original research on the molecular basis of cancer, including articles with translational relevance to diagnosis or therapy. We will include timely reviews covering the broad scope of the journal. The journal will also publish op-ed pieces and meeting reports of interest. The goal is to foster communication and rapid exchange of information through timely publication of important results using traditional as well as electronic formats. The journal and the outstanding Editorial Board will strive to maintain the highest standards for excellence in all activities to generate a valuable resource.
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