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细胞质多聚腺苷酸化元件结合蛋白 1 在肿瘤发生中的作用。

The Roles of Cytoplasmic Polyadenylation Element Binding Protein 1 in Tumorigenesis.

机构信息

Hubei Key Laboratory of Tumor Microenvironment and Immunotherapy, China Three Gorges University.

College of Basic Medical Science, China Three Gorges University, Yichang 443002, China.

出版信息

Mini Rev Med Chem. 2024;24(22):2008-2018. doi: 10.2174/0113895575293544240605112838.

DOI:10.2174/0113895575293544240605112838
PMID:38879767
Abstract

BACKGROUND

CPEB1 is an alternative polyadenylation binding protein that promotes or suppresses the expression of related mRNAs and proteins by binding to a highly conserved Cytoplasmic Polyadenylation Element (CPE) in the mRNAs 3'UTR. It is found to express abnormally in multiple tumors and affect tumorigenesis through many pathways. This review summarizes the functions and mechanisms of CPEB1 in a variety of cancers and suggests new directions for future related treatments.

METHODS

A total of 95 articles were eligible for inclusion based on the year, quality of the research, and the strength of association with CPEB1. In this review, current research about how CPEB1 affects the initiation and progression of glioblastoma, breast cancer, hepatocellular carcinoma, gastric cancer, colorectal cancer, non-small cell lung cancer, prostate cancer, and melanoma are dissected, and the biomedical functions and mechanisms are summarized.

RESULTS

CPEB1 mostly presents as a tumor suppressor for breast cancer, endometrial carcinoma, hepatocellular carcinoma, non-small cell lung cancer, prostate cancer, and melanoma. However, for glioblastoma, gastric cancer, and colorectal cancer, CPEB1 exhibts two opposing properties of tumorigenesis, either promoting or inhibiting it.

CONCLUSION

CPEB1 is likely to serve as a target and dynamic detection index or prognostic indicator for its function of apoptosis, activity, proliferation, migration, invasion, stemness, drug resistance, and even ferroptosis in various cancers.

摘要

背景

CPEB1 是一种另类聚腺苷酸化结合蛋白,通过与 mRNA 3'UTR 中的高度保守的细胞质聚腺苷酸化元件(CPE)结合,促进或抑制相关 mRNA 和蛋白质的表达。它在多种肿瘤中异常表达,并通过多种途径影响肿瘤发生。本综述总结了 CPEB1 在多种癌症中的功能和机制,并为未来相关治疗提出了新的方向。

方法

根据研究年份、研究质量和与 CPEB1 关联的强度,共纳入 95 篇符合条件的文章。在本综述中,我们剖析了 CPEB1 如何影响脑胶质瘤、乳腺癌、肝癌、胃癌、结直肠癌、非小细胞肺癌、前列腺癌和黑色素瘤的发生和发展,并总结了其生物医学功能和机制。

结果

CPEB1 主要作为乳腺癌、子宫内膜癌、肝癌、非小细胞肺癌、前列腺癌和黑色素瘤的肿瘤抑制因子发挥作用。然而,对于脑胶质瘤、胃癌和结直肠癌,CPEB1 表现出两种相反的促癌特性。

结论

CPEB1 可能作为各种癌症中凋亡、活性、增殖、迁移、侵袭、干性、耐药性甚至铁死亡等功能的靶点和动态检测指标或预后标志物。

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The Roles of Cytoplasmic Polyadenylation Element Binding Protein 1 in Tumorigenesis.细胞质多聚腺苷酸化元件结合蛋白 1 在肿瘤发生中的作用。
Mini Rev Med Chem. 2024;24(22):2008-2018. doi: 10.2174/0113895575293544240605112838.
2
CPEB1 regulates the expression of MTDH/AEG-1 and glioblastoma cell migration.CPEB1 调控 MTDH/AEG-1 的表达并影响胶质母细胞瘤细胞迁移。
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3
MicroRNA-183 induces epithelial-mesenchymal transition and promotes endometrial cancer cell migration and invasion in by targeting CPEB1.MicroRNA-183 通过靶向 CPEB1 诱导上皮-间充质转化并促进子宫内膜癌细胞迁移和侵袭。
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CPEB1 restrains proliferation of Glioblastoma cells through the regulation of p27(Kip1) mRNA translation.CPEB1通过调控p27(Kip1)mRNA翻译来抑制胶质母细胞瘤细胞的增殖。
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Cytoplasmic polyadenylation and cytoplasmic polyadenylation element-dependent mRNA regulation are involved in Xenopus retinal axon development.胞质聚腺苷酸化及依赖胞质聚腺苷酸化元件的mRNA调控参与非洲爪蟾视网膜轴突发育。
Neural Dev. 2009 Mar 2;4:8. doi: 10.1186/1749-8104-4-8.
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CPEB1 coordinates alternative 3'-UTR formation with translational regulation.CPEB1 通过与翻译调控协调 3'-UTR 形成。
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本文引用的文献

1
Disruption of Zar1 leads to arrested oogenesis by regulating polyadenylation via Cpeb1 in tilapia (Oreochromis niloticus).Zar1 的缺失通过 Cpeb1 调控多聚腺苷酸化从而导致罗非鱼(Oreochromis niloticus)卵母细胞发生有丝分裂阻滞。
Int J Biol Macromol. 2024 Mar;260(Pt 2):129632. doi: 10.1016/j.ijbiomac.2024.129632. Epub 2024 Jan 20.
2
Vaping, Environmental Toxicants Exposure, and Lung Cancer Risk.电子烟使用、环境毒物暴露与肺癌风险
Cancers (Basel). 2023 Sep 12;15(18):4525. doi: 10.3390/cancers15184525.
3
YY1-regulated lncRNA SOCS2-AS1 suppresses HCC cell stemness and progression via miR-454-3p/CPEB1.
YY1 调控的 lncRNA SOCS2-AS1 通过 miR-454-3p/CPEB1 抑制 HCC 细胞干性和进展。
Biochem Biophys Res Commun. 2023 Oct 30;679:98-109. doi: 10.1016/j.bbrc.2023.08.056. Epub 2023 Aug 26.
4
Knockdown of CPEB1 and CPEB4 Inhibits Scar Formation via Modulation of TAK1 and SMAD Signaling.敲低CPEB1和CPEB4通过调节TAK1和SMAD信号通路抑制瘢痕形成。
Ann Dermatol. 2023 Aug;35(4):293-302. doi: 10.5021/ad.22.210.
5
PATL2 regulates mRNA homeostasis in oocytes by interacting with EIF4E and CPEB1.PATL2 通过与 EIF4E 和 CPEB1 相互作用来调节卵母细胞中的 mRNA 动态平衡。
Development. 2023 Jun 15;150(12). doi: 10.1242/dev.201572. Epub 2023 Jun 13.
6
CPEB and translational control by cytoplasmic polyadenylation: impact on synaptic plasticity, learning, and memory.CPEB 和细胞质多聚腺苷酸化的翻译控制:对突触可塑性、学习和记忆的影响。
Mol Psychiatry. 2023 Jul;28(7):2728-2736. doi: 10.1038/s41380-023-02088-x. Epub 2023 May 2.
7
Predictors of early and late hepatocellular carcinoma recurrence.预测早期和晚期肝细胞癌复发的因素。
World J Gastroenterol. 2023 Feb 28;29(8):1243-1260. doi: 10.3748/wjg.v29.i8.1243.
8
Author Correction: CPEB1-dependent disruption of the mRNA translation program in oocytes during maternal aging.作者更正:母体衰老过程中卵母细胞中依赖CPEB1的mRNA翻译程序破坏。
Nat Commun. 2023 Feb 6;14(1):646. doi: 10.1038/s41467-023-36396-1.
9
Lipid Peroxidation and Iron Metabolism: Two Corner Stones in the Homeostasis Control of Ferroptosis.脂质过氧化作用和铁代谢:铁死亡体内平衡调控的两个基石。
Int J Mol Sci. 2022 Dec 27;24(1):449. doi: 10.3390/ijms24010449.
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Hepatocellular Carcinoma: New Developments.肝细胞癌:新进展。
Clin Liver Dis. 2023 Feb;27(1):85-102. doi: 10.1016/j.cld.2022.08.004. Epub 2022 Oct 18.