a Epigenetics Institute, Department of Biochemistry and Biophysics, Perelman School of Medicine , University of Pennsylvania , Philadelphia , PA , USA.
b Department of Pathology and Laboratory Medicine, Perelman School of Medicine , University of Pennsylvania , Philadelphia , PA , USA.
Expert Rev Proteomics. 2019 Jan;16(1):33-47. doi: 10.1080/14789450.2019.1550363. Epub 2018 Nov 27.
: Epigenetic dysregulation drives or supports numerous human cancers. The chromatin landscape in cancer cells is often marked by abnormal histone post-translational modification (PTM) patterns and by aberrant assembly and recruitment of protein complexes to specific genomic loci. Mass spectrometry-based proteomic analyses can support the discovery and characterization of both phenomena. : We broadly divide this literature into two parts: 'modification-centric' analyses that link histone PTMs to cancer biology; and 'complex-centric' analyses that examine protein-protein interactions that occur as a result of oncogenic mutations. We also discuss proteomic studies of oncohistones. We highlight relevant examples, discuss limitations, and speculate about forthcoming innovations regarding each application. : 'Modification-centric' analyses have been used to further understanding of cancer's histone code and to identify associated therapeutic vulnerabilities. 'Complex-centric' analyses have likewise revealed insights into mechanisms of oncogenesis and suggested potential therapeutic targets, particularly in MLL-associated leukemia. Proteomic experiments have also supported some of the pioneering studies of oncohistone-mediated tumorigenesis. Additional applications of proteomics that may benefit cancer epigenetics research include middle-down and top-down histone PTM analysis, chromatin reader profiling, and genomic locus-specific protein identification. In the coming years, proteomic approaches will remain powerful ways to interrogate the biology of cancer.
表观遗传失调驱动或支持着许多人类癌症。癌细胞中的染色质景观通常表现为异常的组蛋白翻译后修饰(PTM)模式,以及异常的蛋白复合物组装和募集到特定的基因组位点。基于质谱的蛋白质组学分析可以支持这两种现象的发现和特征描述。
“修饰为中心”的分析将组蛋白 PTM 与癌症生物学联系起来;“复合物为中心”的分析研究了由于致癌突变而发生的蛋白-蛋白相互作用。我们还讨论了癌蛋白组学的研究。我们突出了相关的例子,讨论了局限性,并对每种应用的未来创新进行了推测。
“修饰为中心”的分析已被用于进一步了解癌症的组蛋白密码,并确定相关的治疗弱点。“复合物为中心”的分析同样揭示了致癌机制的见解,并提出了潜在的治疗靶点,特别是在 MLL 相关的白血病中。蛋白质组学实验也支持了一些关于癌蛋白介导的肿瘤发生的开创性研究。蛋白质组学的其他应用可能有益于癌症表观遗传学研究,包括中肽和从头组蛋白 PTM 分析、染色质读取器分析和基因组特定位点的蛋白质鉴定。在未来几年,蛋白质组学方法将仍然是研究癌症生物学的有力工具。