Rabbitts T H
MRC Laboratory of Molecular Biology, Cambridge, UK.
Nature. 1994 Nov 10;372(6502):143-9. doi: 10.1038/372143a0.
Chromosomal abnormalities in tumours were recognized at the end of the last century but their significance has only recently become clear. Distinct translocations in leukaemias and in solid tumours lead to the activation of proto-oncogene products or, more commonly, creation of tumour-specific fusion proteins. The proteins in both categories are often transcription factors and thus disruption of transcriptional control plays a major role in the aetiology of cancer. Fusion proteins formed after chromosomal translocations are common in a range of tumour types; these are unique tumour antigens and are therefore potential targets for therapy design.
肿瘤中的染色体异常在19世纪末就已被发现,但直到最近其重要性才变得清晰。白血病和实体瘤中不同的易位会导致原癌基因产物的激活,或者更常见的是产生肿瘤特异性融合蛋白。这两类蛋白质通常都是转录因子,因此转录控制的破坏在癌症病因学中起着主要作用。染色体易位后形成的融合蛋白在一系列肿瘤类型中都很常见;这些是独特的肿瘤抗原,因此是治疗设计的潜在靶点。