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综合生物信息学分析揭示 miR-524-5p/MEF2C 调控前列腺癌和乳腺癌的骨转移。

Integrative Bioinformatics Analysis Reveals That miR-524-5p/MEF2C Regulates Bone Metastasis in Prostate Cancer and Breast Cancer.

机构信息

Department of Diagnostic and Interventional Radiology, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai, China.

出版信息

Comput Math Methods Med. 2022 Sep 10;2022:5211329. doi: 10.1155/2022/5211329. eCollection 2022.

Abstract

Bone metastases are highly prevalent in patients with advanced prostate cancer and breast cancer and have a serious impact on the survival time and quality of life of these patients. It has been reported that microRNAs (miRNAs) are expressed abnormally in different types of cancer and metastases. However, it remains unknown whether the underlying miRNAs are associated with prostate and breast cancer bone metastasis. Differentially expressed miRNAs (DE-miRNAs) and their potential targets in the metastatic process were identified by bioinformatics analysis. Additionally, qPCR confirmed that the miR-524-5p expression was downregulated in prostate and breast cancer cells. The overexpression of miR-524-5p restrained cell proliferation, invasion, and metastasis in prostate and breast cancer cells. Meanwhile, miR-524-5p could target and inhibit the expression of MEF2C, which was verified by a luciferase assay. In conclusion, our data strongly suggest that downregulation of miR-524-5p appears to be a precocious event in prostate and breast cancer, and the miR-524-5p/MEF2C axis plays a novel role in bone metastases from prostate and breast cancers.

摘要

骨转移在晚期前列腺癌和乳腺癌患者中非常普遍,严重影响了这些患者的生存时间和生活质量。据报道,微小 RNA(miRNA)在不同类型的癌症和转移中表达异常。然而,尚不清楚潜在的 miRNA 是否与前列腺癌和乳腺癌的骨转移有关。通过生物信息学分析鉴定了转移性过程中差异表达的 miRNA(DE-miRNA)及其潜在靶标。此外,qPCR 证实 miR-524-5p 在前列腺癌和乳腺癌细胞中的表达下调。miR-524-5p 的过表达抑制了前列腺癌和乳腺癌细胞的增殖、侵袭和转移。同时,miR-524-5p 可以靶向并抑制 MEF2C 的表达,这通过荧光素酶测定得到了验证。总之,我们的数据强烈表明,miR-524-5p 的下调似乎是前列腺癌和乳腺癌的早期事件,miR-524-5p/MEF2C 轴在前列腺癌和乳腺癌的骨转移中发挥了新的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea83/9482681/9fdca0184e10/CMMM2022-5211329.001.jpg

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