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核激活微小RNA:揭示癌症和免疫疾病中亚细胞微小RNA功能与调控的复杂性

Nuclear-activating miRNAs: unveiling the intricacies of subcellular miRNA function and regulation in cancer and immunity disease.

作者信息

Ren Xiang, Liu Gang, Zhou Jianping

机构信息

Department of Gastrointestinal Surgery, The First Hospital of China Medical University, Nanjing Street 155, Shenyang, 110001, China.

Department of Colorectal Hernia Surgery, Binzhou Medical University Hospital, Yantai, China.

出版信息

Cancer Cell Int. 2025 Apr 15;25(1):147. doi: 10.1186/s12935-025-03760-8.

DOI:10.1186/s12935-025-03760-8
PMID:40234876
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11998458/
Abstract

MicroRNAs (miRNAs) are small non-coding RNAs that traditionally recognized as negative regulators of gene expression through post-transcriptional regulation in the cytoplasm. However, recent discoveries have unveiled some novel miRNA functions in the cell nucleus, where a subset of miRNAs, termed nuclear-activating miRNAs (NamiRNAs), play pivotal roles in gene activation and transcriptional regulation for cancer and immunity disease. The discovery of NamiRNAs demonstrated a complementary regulatory function of miRNA, showing their differential activities in the nucleus and cytoplasm. This review aims to explore the biogenesis, mechanisms, and regulatory functions of NamiRNAs, deciphering their involvement in NamiRNA-gene network for gene expression modulation, and emerging significance as drug targets against cancer.

摘要

微小RNA(miRNA)是一类小的非编码RNA,传统上被认为是通过细胞质中的转录后调控来作为基因表达的负调节因子。然而,最近的发现揭示了miRNA在细胞核中的一些新功能,其中一部分被称为核激活微小RNA(NamiRNA)的miRNA在癌症和免疫疾病的基因激活和转录调控中发挥着关键作用。NamiRNA的发现证明了miRNA的一种互补调节功能,显示了它们在细胞核和细胞质中的不同活性。本综述旨在探讨NamiRNA的生物发生、机制和调控功能,解读它们在NamiRNA-基因网络中对基因表达调控的参与情况,以及作为抗癌药物靶点的新意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b93c/11998458/fe5d22f67543/12935_2025_3760_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b93c/11998458/da57d2a62b94/12935_2025_3760_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b93c/11998458/fe5d22f67543/12935_2025_3760_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b93c/11998458/da57d2a62b94/12935_2025_3760_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b93c/11998458/fe5d22f67543/12935_2025_3760_Fig2_HTML.jpg

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本文引用的文献

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Nuclear miR-150 enhances hepatic lipid accumulation by targeting RNA transcripts overlapping the promoter.核内微小RNA-150通过靶向与启动子重叠的RNA转录本来增强肝脏脂质积累。
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Recent advances in the functional explorations of nuclear microRNAs.核微小 RNA 功能探索的最新进展。
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NamiRNA-enhancer network of miR-492 activates the NR2C1-TGF-β/Smad3 pathway to promote epithelial-mesenchymal transition of pancreatic cancer.
miR-492 的 NamiRNA 增强子网络激活 NR2C1-TGF-β/Smad3 通路促进胰腺癌上皮间质转化。
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miR-24-1/enhancer axis activation blocks renal cell carcinoma progression Warburg effect.miR-24-1/增强子轴激活可阻断肾细胞癌进展及瓦伯格效应。
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Tumor suppressor genes are reactivated by miR-26A1 via enhancer reprogramming in NSCLC.抑癌基因通过 miR-26A1 在非小细胞肺癌中通过增强子重编程被重新激活。
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Reactivation of tumour suppressor in breast cancer by enhancer switching through NamiRNA network.通过 NamiRNA 网络的增强子切换实现乳腺癌中肿瘤抑制因子的再激活。
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