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-甲基腺苷结合蛋白异质核糖核蛋白A2B1在人类癌症中的生物学功能及研究进展

Biological function and research progress of -methyladenosine binding protein heterogeneous nuclear ribonucleoprotein A2B1 in human cancers.

作者信息

Wu Yue, Li An, Chen Can, Fang Zhang, Chen Lujun, Zheng Xiao

机构信息

Department of Tumor Biological Treatment, The Third Affiliated Hospital of Soochow University, Changzhou, Jiangsu, China.

Jiangsu Engineering Research Center for Tumor Immunotherapy, The Third Affiliated Hospital of Soochow University, Changzhou, Jiangsu, China.

出版信息

Front Oncol. 2023 Jul 20;13:1229168. doi: 10.3389/fonc.2023.1229168. eCollection 2023.

DOI:10.3389/fonc.2023.1229168
PMID:37546413
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10399595/
Abstract

N-methyladenosine (mA) is the most prevalent internal modification found in both mRNA and lncRNA. It exerts reversible regulation over RNA function and affects RNA processing and metabolism in various diseases, especially tumors. The mA binding protein, hnRNPA2B1, is extensively studied as a member of the heterogeneous nuclear ribonucleoprotein (hnRNP) protein family. It is frequently dysregulated and holds significant importance in multiple types of tumors. By recognizing mA sites for variable splicing, maintaining RNA stability, and regulating translation and transport, hnRNPA2B1 plays a vital role in various aspects of tumor development, metabolism, and regulation of the immune microenvironment. In this review, we summarized the latest research on the functional roles and underlying molecular mechanisms of hnRNPA2B1. Moreover, we discussed its potential as a target for tumor therapy.

摘要

N6-甲基腺苷(mA)是在信使核糖核酸(mRNA)和长链非编码核糖核酸(lncRNA)中发现的最普遍的内部修饰。它对RNA功能进行可逆调节,并影响多种疾病,尤其是肿瘤中的RNA加工和代谢。mA结合蛋白hnRNPA2B1作为异质性核糖核蛋白(hnRNP)家族的成员被广泛研究。它经常失调,在多种类型的肿瘤中具有重要意义。通过识别可变剪接的mA位点、维持RNA稳定性以及调节翻译和转运,hnRNPA2B1在肿瘤发生发展、代谢以及免疫微环境调节的各个方面发挥着至关重要的作用。在本综述中,我们总结了关于hnRNPA2B1功能作用及潜在分子机制的最新研究。此外,我们还讨论了其作为肿瘤治疗靶点的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d7d/10399595/1afb9fed3888/fonc-13-1229168-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d7d/10399595/8f8b60673069/fonc-13-1229168-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d7d/10399595/132c5ad708a9/fonc-13-1229168-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d7d/10399595/1afb9fed3888/fonc-13-1229168-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d7d/10399595/8f8b60673069/fonc-13-1229168-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d7d/10399595/132c5ad708a9/fonc-13-1229168-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d7d/10399595/1afb9fed3888/fonc-13-1229168-g003.jpg

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本文引用的文献

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Lung adenocarcinoma cell-derived exosomes promote M2 macrophage polarization through transmission of miR-3153 to activate the JNK signaling pathway.肺腺癌细胞衍生的外泌体通过传递 miR-3153 促进 M2 巨噬细胞极化,从而激活 JNK 信号通路。
Hum Mol Genet. 2023 Jun 19;32(13):2162-2176. doi: 10.1093/hmg/ddad052.
2
Exosome-derived circCCAR1 promotes CD8 + T-cell dysfunction and anti-PD1 resistance in hepatocellular carcinoma.外泌体来源的 circCCAR1 促进肝癌中 CD8+T 细胞功能障碍和抗 PD1 耐药性。
Mol Cancer. 2023 Mar 18;22(1):55. doi: 10.1186/s12943-023-01759-1.
3
Targeting mA reader YTHDF1 augments antitumour immunity and boosts anti-PD-1 efficacy in colorectal cancer.
靶向 mA 读者 YTHDF1 增强抗肿瘤免疫并提高结直肠癌的抗 PD-1 疗效。
Gut. 2023 Aug;72(8):1497-1509. doi: 10.1136/gutjnl-2022-328845. Epub 2023 Jan 30.
4
Exon architecture controls mRNA mA suppression and gene expression.外显子结构控制 mRNA 的 mA 抑制和基因表达。
Science. 2023 Feb 17;379(6633):677-682. doi: 10.1126/science.abj9090. Epub 2023 Jan 27.
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Chemo-drugs in cell microparticles reset antitumor activity of macrophages by activating lysosomal P450 and nuclear hnRNPA2B1.细胞微粒中的化疗药物通过激活溶酶体 P450 和核 hnRNPA2B1 来重新激活巨噬细胞的抗肿瘤活性。
Signal Transduct Target Ther. 2023 Jan 20;8(1):22. doi: 10.1038/s41392-022-01212-7.
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Exclusion of m6A from splice-site proximal regions by the exon junction complex dictates m6A topologies and mRNA stability.外显子连接复合体将m6A排除在剪接位点近端区域之外,决定了m6A的拓扑结构和mRNA稳定性。
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