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剪接因子在激素相关癌症进展中的作用。

Roles of Splicing Factors in Hormone-Related Cancer Progression.

机构信息

Division of Gene Regulation and Signal Transduction, Research Center for Genomic Medicine, Saitama Medical University, Hidaka, Saitama 350-1241, Japan.

Department of Systems Aging Science and Medicine, Tokyo Metropolitan Institute of Gerontology, Itabashi-ku, Tokyo 173-0015, Japan.

出版信息

Int J Mol Sci. 2020 Feb 25;21(5):1551. doi: 10.3390/ijms21051551.

DOI:10.3390/ijms21051551
PMID:32106418
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7084890/
Abstract

Splicing of mRNA precursor (pre-mRNA) is a mechanism to generate multiple mRNA isoforms from a single pre-mRNA, and it plays an essential role in a variety of biological phenomena and diseases such as cancers. Previous studies have demonstrated that cancer-specific splicing events are involved in various aspects of cancers such as proliferation, migration and response to hormones, suggesting that splicing-targeting therapy can be promising as a new strategy for cancer treatment. In this review, we focus on the splicing regulation by RNA-binding proteins including Drosophila behavior/human splicing (DBHS) family proteins, serine/arginine-rich (SR) proteins and heterogeneous nuclear ribonucleoproteins (hnRNPs) in hormone-related cancers, such as breast and prostate cancers.

摘要

mRNA 前体(pre-mRNA)的剪接是一种从单个 pre-mRNA 生成多种 mRNA 异构体的机制,它在各种生物现象和疾病中起着至关重要的作用,如癌症。先前的研究表明,癌症特异性剪接事件涉及癌症的各个方面,如增殖、迁移和对激素的反应,这表明剪接靶向治疗可能是癌症治疗的一种有前途的新策略。在这篇综述中,我们重点介绍了 RNA 结合蛋白(包括果蝇行为/人类剪接(DBHS)家族蛋白、丝氨酸/精氨酸丰富(SR)蛋白和核不均一核糖核蛋白(hnRNPs))对激素相关癌症(如乳腺癌和前列腺癌)中的剪接调控。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a024/7084890/af45bc47bf5a/ijms-21-01551-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a024/7084890/3d81554d4301/ijms-21-01551-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a024/7084890/3d4b15e110ac/ijms-21-01551-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a024/7084890/af45bc47bf5a/ijms-21-01551-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a024/7084890/3d81554d4301/ijms-21-01551-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a024/7084890/3d4b15e110ac/ijms-21-01551-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a024/7084890/af45bc47bf5a/ijms-21-01551-g003.jpg

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Aberrant Splicing as a Mechanism for Resistance to Cancer Therapies.异常剪接作为癌症治疗耐药的一种机制
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本文引用的文献

1
Differential Functions of Splicing Factors in Mammary Transformation and Breast Cancer Metastasis.剪接因子在乳腺转化和乳腺癌转移中的差异功能。
Cell Rep. 2019 Nov 26;29(9):2672-2688.e7. doi: 10.1016/j.celrep.2019.10.110.
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RNA-binding protein NONO promotes breast cancer proliferation by post-transcriptional regulation of SKP2 and E2F8.RNA 结合蛋白 NONO 通过 SKP2 和 E2F8 的转录后调控促进乳腺癌增殖。
Cancer Sci. 2020 Jan;111(1):148-159. doi: 10.1111/cas.14240. Epub 2019 Dec 11.
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Recurrent noncoding U1 snRNA mutations drive cryptic splicing in SHH medulloblastoma.
综合系统生物学分析揭示剪接因子对皮肤黑色素瘤进展的作用。
Sci Rep. 2025 Mar 19;15(1):9486. doi: 10.1038/s41598-025-93695-x.
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Alternative splicing in ovarian cancer.卵巢癌中的可变剪接。
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Alternative Splicing Landscape of Head and Neck Squamous Cell Carcinoma.头颈部鳞状细胞癌的可变剪接图谱
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Role of RNA binding proteins of the behavior and human splicing (DBHS) family in health and cancer.行为和人类剪接(DBHS)家族的 RNA 结合蛋白在健康和癌症中的作用。
RNA Biol. 2024 Jan;21(1):1-17. doi: 10.1080/15476286.2024.2332855. Epub 2024 Mar 29.
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Roles and mechanisms of aberrant alternative splicing in melanoma - implications for targeted therapy and immunotherapy resistance.异常可变剪接在黑色素瘤中的作用和机制——对靶向治疗和免疫治疗耐药性的影响
Cancer Cell Int. 2024 Mar 10;24(1):101. doi: 10.1186/s12935-024-03280-x.
8
Established and Evolving Roles of the Multifunctional Non-POU Domain-Containing Octamer-Binding Protein (NonO) and Splicing Factor Proline- and Glutamine-Rich (SFPQ).多功能非POU结构域含八聚体结合蛋白(NonO)和富含脯氨酸和谷氨酰胺的剪接因子(SFPQ)的既定作用与演变作用
J Dev Biol. 2024 Jan 5;12(1):3. doi: 10.3390/jdb12010003.
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Pre-mRNA splicing-associated diseases and therapies.前体 mRNA 剪接相关疾病和治疗方法。
RNA Biol. 2023 Jan;20(1):525-538. doi: 10.1080/15476286.2023.2239601.
10
[Construction of an adenovirus vector expressing engineered splicing factor for regulating alternative splicing of YAP1 in neonatal rat cardiomyocytes].[构建用于调控新生大鼠心肌细胞中YAP1可变剪接的表达工程化剪接因子的腺病毒载体]
Nan Fang Yi Ke Da Xue Xue Bao. 2022 Jul 20;42(7):1013-1018. doi: 10.12122/j.issn.1673-4254.2022.07.07.
U1 snRNA 基因的非编码区反复突变导致 SHH 型髓母细胞瘤剪接异常。
Nature. 2019 Oct;574(7780):707-711. doi: 10.1038/s41586-019-1650-0. Epub 2019 Oct 9.
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The U1 spliceosomal RNA is recurrently mutated in multiple cancers.U1 剪接体 RNA 在多种癌症中经常发生突变。
Nature. 2019 Oct;574(7780):712-716. doi: 10.1038/s41586-019-1651-z. Epub 2019 Oct 9.
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Androgen receptor splicing variant 7: Beyond being a constitutively active variant.雄激素受体剪接变异体 7:不仅仅是一种组成型激活变异体。
Life Sci. 2019 Oct 1;234:116768. doi: 10.1016/j.lfs.2019.116768. Epub 2019 Aug 21.
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SF3B2-Mediated RNA Splicing Drives Human Prostate Cancer Progression.SF3B2 介导的 RNA 剪接驱动人类前列腺癌进展。
Cancer Res. 2019 Oct 15;79(20):5204-5217. doi: 10.1158/0008-5472.CAN-18-3965. Epub 2019 Aug 20.
7
Spliceosome component SF3B1 as novel prognostic biomarker and therapeutic target for prostate cancer.剪接体复合物 SF3B1 作为前列腺癌的新型预后生物标志物和治疗靶点。
Transl Res. 2019 Oct;212:89-103. doi: 10.1016/j.trsl.2019.07.001. Epub 2019 Jul 9.
8
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Selective Androgen Receptor Modulators: Current Knowledge and Clinical Applications.选择性雄激素受体调节剂:当前知识与临床应用。
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Regulation of Mcl-1 alternative splicing by hnRNP F, H1 and K in breast cancer cells.hnRNP F、H1 和 K 调控乳腺癌细胞中 Mcl-1 的可变剪接。
RNA Biol. 2018;15(12):1448-1457. doi: 10.1080/15476286.2018.1551692. Epub 2018 Dec 4.