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癌症与减数分裂基因表达:同一枚硬币的两面?

Cancer and meiotic gene expression: Two sides of the same coin?

机构信息

Institute of Systems, Molecular and Integrative Biology, University of Liverpool, Liverpool, United Kingdom; Chromatin Dynamics and Disease Epigenetics Group, Institute of Molecular and Cell Biology, Agency for Science, Technology and Research (A*STAR), Singapore, Singapore.

Center for Reproductive Medicine, Reproductive Biology Laboratory, Amsterdam Reproduction and Development Research Institute, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.

出版信息

Curr Top Dev Biol. 2023;151:43-68. doi: 10.1016/bs.ctdb.2022.06.002. Epub 2022 Jul 29.

Abstract

Meiosis increases genetic diversity in offspring by generating genetically unique haploid gametes with reshuffled chromosomes. This process requires a specialized set of meiotic proteins, which facilitate chromosome recombination and segregation. However, re-expression of meiotic proteins in mitosis can have catastrophic oncogenic consequences and aberrant expression of meiotic proteins is a common occurrence in human tumors. Mechanistically, re-activation of meiotic genes in cancer promotes oncogenesis likely because cancers-conversely to healthy mitosis-are fueled by genetic instability which promotes tumor evolution, and evasion of immune response and treatment pressure. In this review, we explore similarities between meiotic and cancer cells with a particular focus on the oncogenic activation of meiotic genes in cancer. We emphasize the role of histones and their modifications, DNA methylation, genome organization, R-loops and the availability of distal enhancers.

摘要

减数分裂通过生成染色体重排的遗传独特的单倍体配子来增加后代的遗传多样性。这个过程需要一组专门的减数分裂蛋白,它们促进染色体重组和分离。然而,减数分裂蛋白在有丝分裂中的重新表达可能会产生灾难性的致癌后果,减数分裂蛋白的异常表达在人类肿瘤中很常见。从机制上讲,减数分裂基因在癌症中的重新激活可能促进了肿瘤的发生,因为癌症与健康的有丝分裂相反,是由遗传不稳定性推动的,这种不稳定性促进了肿瘤的进化,以及逃避免疫反应和治疗压力。在这篇综述中,我们探讨了减数分裂细胞和癌细胞之间的相似之处,特别关注了减数分裂基因在癌症中的致癌激活。我们强调了组蛋白及其修饰、DNA 甲基化、基因组组织、R-环和远端增强子的可用性的作用。

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