癌症多重宇宙中的组蛋白 H3 变异

Iva Simeonova, Geneviève Almouzni
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摘要

我们对癌症基因组的了解使我们能够将分子数据整合到组织病理学分类中,对患者进行常规分层。在过去的 10-15 年中,得益于大规模测序的系统实施,组蛋白基因中热点体细胞突变的鉴定进入了人们的视线,凸显了oncohistones 的概念。作为小儿脑肿瘤和其他几种癌症的驱动因素,组蛋白基因突变为癌症的多重宇宙带来了 "新的奇异维度",用惊奇公司的话说就是 "新的奇异维度"。癌症的复杂性是一个多维投影,迫切需要一种综合方法来考虑所有相关的病因、发育和进化因素。在此,我们将讨论组蛋白变异和伴侣、它们在癌症中的调控和改变、可用的体内模型以及当前的治疗策略等方面的最新进展。更具体地说,我们将从组织特异性差异以及基因组表达和完整性维护手段的角度进行分析。
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Histone H3 Variants in the Multiverse of Cancer
Our understanding of cancer genomes has allowed for the integration of molecular data into histopathological classifications for routine stratification of patients. In the last 10–15 years, thanks to this systematic implementation of large-scale sequencing, the identification of hotspot somatic mutations in histone genes came into the limelight, underscoring the concept of oncohistones. As drivers in pediatric brain tumors, and in several other types of cancers, oncohistones brought a “new dimension of Strange” into the cancer multiverse, to paraphrase Marvel. An integrative approach to cancer complexity as a multidimensional projection is urgently needed to consider all relevant etiological, developmental, and evolutionary components. Here, we discuss recent progress on histone variants and chaperones, their regulation and alterations in cancers, the available in vivo models, and current treatment strategies. More specifically, we adopt a view through the lens of tissue-specific differences and means for genome expression and integrity maintenance.
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