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微小RNA作为大脑健康与疾病的主要参与者:当前认知与未来展望

MiRNAs as major players in brain health and disease: current knowledge and future perspectives.

作者信息

Kapplingattu Sarika V, Bhattacharya Sujata, Adlakha Yogita K

机构信息

Amity Institute of Molecular Medicine and Stem Cell Research, Amity University, Noida, Uttar Pradesh 201303, India.

出版信息

Cell Death Discov. 2025 Jan 13;11(1):7. doi: 10.1038/s41420-024-02283-x.

Abstract

MicroRNAs are regulators of gene expression and their dysregulation can lead to various diseases. MicroRNA-135 (MiR-135) exhibits brain-specific expression, and performs various functions such as neuronal morphology, neural induction, and synaptic function in the human brain. Dysfunction of miR-135 has been reported in brain tumors, and neurodegenerative and neurodevelopmental disorders. Several reports show downregulation of miR-135 in glioblastoma, indicating its tumor suppressor role in the pathogenesis of brain tumors. In this review, by performing in silico analysis of molecular targets of miR-135, we reveal the significant pathways and processes modulated by miR-135. We summarize the biological significance, roles, and signaling pathways of miRNAs in general, with a focus on miR-135 in different neurological diseases including brain tumors, and neurodegenerative and neurodevelopmental disorders. We also discuss methods, limitations, and potential of glioblastoma organoids in recapitulating disease initiation and progression. We highlight the promising therapeutic potential of miRNAs as antitumor agents for aggressive human brain tumors including glioblastoma.

摘要

微小RNA是基因表达的调节因子,其失调可导致多种疾病。微小RNA-135(MiR-135)表现出脑特异性表达,并在人脑中发挥多种功能,如神经元形态、神经诱导和突触功能。据报道,MiR-135功能障碍与脑肿瘤、神经退行性疾病和神经发育障碍有关。多项报告显示,胶质母细胞瘤中MiR-135表达下调,表明其在脑肿瘤发病机制中具有肿瘤抑制作用。在本综述中,通过对MiR-135的分子靶点进行计算机分析,我们揭示了MiR-135调节的重要途径和过程。我们总结了微小RNA的生物学意义、作用和信号通路,重点关注MiR-135在包括脑肿瘤、神经退行性疾病和神经发育障碍在内的不同神经系统疾病中的作用。我们还讨论了胶质母细胞瘤类器官在重现疾病发生和进展方面的方法、局限性和潜力。我们强调了微小RNA作为侵袭性人脑肿瘤(包括胶质母细胞瘤)抗肿瘤药物的潜在治疗价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf5d/11729916/7f2eb81bf003/41420_2024_2283_Fig1_HTML.jpg

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