Balaji A K, Saha Santam, Deshpande Shruti, Poola Darshini, Sengupta Kundan
Chromosome Biology Lab (CBL), Indian Institute of Science Education and Research, Pune, Maharashtra, India.
Front Cell Dev Biol. 2022 Dec 16;10:1068347. doi: 10.3389/fcell.2022.1068347. eCollection 2022.
In eukaryotic cells, the genome is organized in the form of chromatin composed of DNA and histones that organize and regulate gene expression. The dysregulation of chromatin remodeling, including the aberrant incorporation of histone variants and their consequent post-translational modifications, is prevalent across cancers. Additionally, nuclear envelope proteins are often deregulated in cancers, which impacts the 3D organization of the genome. Altered nuclear morphology, genome organization, and gene expression are defining features of cancers. With advances in single-cell sequencing, imaging technologies, and high-end data mining approaches, we are now at the forefront of designing appropriate small molecules to selectively inhibit the growth and proliferation of cancer cells in a genome- and epigenome-specific manner. Here, we review recent advances and the emerging significance of aberrations in nuclear envelope proteins, histone variants, and oncohistones in deregulating chromatin organization and gene expression in oncogenesis.
在真核细胞中,基因组以染色质的形式存在,染色质由DNA和组蛋白组成,它们组织并调节基因表达。染色质重塑的失调,包括组蛋白变体的异常掺入及其随后的翻译后修饰,在各种癌症中都很普遍。此外,核膜蛋白在癌症中常常失调,这会影响基因组的三维组织。核形态、基因组组织和基因表达的改变是癌症的决定性特征。随着单细胞测序、成像技术和高端数据挖掘方法的进步,我们现在处于设计合适的小分子以基因组和表观基因组特异性方式选择性抑制癌细胞生长和增殖的前沿。在这里,我们综述了核膜蛋白、组蛋白变体和癌组蛋白的异常在肿瘤发生过程中调节染色质组织和基因表达方面的最新进展及其新出现的重要性。