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癌症转移中的表观遗传修饰物。

Epigenetic Modifiers in Cancer Metastasis.

机构信息

Key Laboratory of Molecular Genetics between Kangda College of Nanjing Medical University and Suzhou Medical College of Soochow University, Suzhou 215123, China.

Department of Basic Medicine, Kangda College of Nanjing Medical University, Lianyungang 222000, China.

出版信息

Biomolecules. 2024 Jul 27;14(8):916. doi: 10.3390/biom14080916.

DOI:10.3390/biom14080916
PMID:39199304
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11352731/
Abstract

Metastasis is the primary cause of cancer-related death, with the dissemination and colonization of primary tumor cells at the metastatic site facilitated by various molecules and complex pathways. Understanding the biological mechanisms underlying the metastatic process is critical for the development of effective interventions. Several epigenetic modifications have been identified that play critical roles in regulating cancer metastasis. This review aims to provide a comprehensive summary of recent advances in understanding the role of epigenetic modifiers, including histone modifications, DNA methylation, non-coding RNAs, enhancer reprogramming, chromatin accessibility, and N6-methyladenosine, in metastasis-associated processes, such as epithelial-mesenchymal transition (EMT), cancer cell migration, and invasion. In particular, this review provides a detailed and in-depth description of the role of crosstalk between epigenetic regulators in tumor metastasis. Additionally, we explored the potential and limitations of epigenetics-related target molecules in the diagnosis, treatment, and prognosis of cancer metastasis.

摘要

转移是癌症相关死亡的主要原因,主要肿瘤细胞通过各种分子和复杂途径在转移部位的扩散和定植。了解转移过程中的生物学机制对于开发有效的干预措施至关重要。已经确定了几种表观遗传修饰,它们在调节癌症转移中起着关键作用。本综述旨在全面总结近年来对表观遗传修饰物(包括组蛋白修饰、DNA 甲基化、非编码 RNA、增强子重编程、染色质可及性和 N6-甲基腺苷)在转移相关过程(如上皮-间充质转化(EMT)、癌细胞迁移和侵袭)中的作用的理解的最新进展。特别是,本综述详细深入地描述了表观遗传调节剂在肿瘤转移中的相互作用。此外,我们还探讨了与癌症转移的诊断、治疗和预后相关的表观遗传相关靶分子的潜力和局限性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81cf/11352731/14b2cdafdd05/biomolecules-14-00916-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81cf/11352731/1603685c5e79/biomolecules-14-00916-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81cf/11352731/76e267b16a9f/biomolecules-14-00916-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81cf/11352731/14b2cdafdd05/biomolecules-14-00916-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81cf/11352731/1603685c5e79/biomolecules-14-00916-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81cf/11352731/76e267b16a9f/biomolecules-14-00916-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81cf/11352731/14b2cdafdd05/biomolecules-14-00916-g003.jpg

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本文引用的文献

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Front Cell Dev Biol. 2023 Dec 21;11:1291179. doi: 10.3389/fcell.2023.1291179. eCollection 2023.
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DNA methylation-activated full-length EMX1 facilitates metastasis through EMX1-EGFR-ERK axis in hepatocellular carcinoma.DNA 甲基化激活全长 EMX1 通过 EMX1-EGFR-ERK 轴促进肝癌转移。
Cell Death Dis. 2023 Nov 25;14(11):769. doi: 10.1038/s41419-023-06293-y.
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Targeting DNA methylation and B7-H3 in RB1-deficient and neuroendocrine prostate cancer.
靶向 RB1 缺陷和神经内分泌前列腺癌中的 DNA 甲基化和 B7-H3。
Sci Transl Med. 2023 Nov 15;15(722):eadf6732. doi: 10.1126/scitranslmed.adf6732.
4
Histone acetyltransferase CSRP2BP promotes the epithelial-mesenchymal transition and metastasis of cervical cancer cells by activating N-cadherin.组蛋白乙酰转移酶 CSRP2BP 通过激活 N-钙黏蛋白促进宫颈癌上皮间质转化和转移。
J Exp Clin Cancer Res. 2023 Oct 17;42(1):268. doi: 10.1186/s13046-023-02839-2.
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Methylated Nucleotide-Based Proteolysis-Targeting Chimera Enables Targeted Degradation of Methyl-CpG-Binding Protein 2.基于甲基化核苷酸的蛋白水解靶向嵌合体可实现甲基化 CpG 结合蛋白 2 的靶向降解。
J Am Chem Soc. 2023 Oct 11;145(40):21871-21878. doi: 10.1021/jacs.3c06023. Epub 2023 Sep 29.
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Super Enhancer-Regulated LncRNA LINC01089 Induces Alternative Splicing of DIAPH3 to Drive Hepatocellular Carcinoma Metastasis.超级增强子调控的长链非编码 RNA LINC01089 诱导 DIAPH3 的可变剪接从而驱动肝癌转移。
Cancer Res. 2023 Dec 15;83(24):4080-4094. doi: 10.1158/0008-5472.CAN-23-0544.
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Epigenomic analysis reveals a unique DNA methylation program of metastasis-competent circulating tumor cells in colorectal cancer.表观基因组分析揭示了结直肠癌中具有转移能力的循环肿瘤细胞独特的 DNA 甲基化程序。
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