Hanks Sandra, Rahman Nazneen
Section of Cancer Genetics, Institute of Cancer Research, Sutton, Surrey, UK.
Cell Cycle. 2005 Feb;4(2):225-7. Epub 2005 Feb 3.
Genetic cancer predisposition syndromes have been crucial to the identification of genes and pathways involved in carcinogenesis. Constitutional gene mutations segregating with distinctive cancer phenotypes provide unequivocal evidence of a gene's causal role in cancer. This type of evidence has been central in proving that oncogenes and tumor suppressor genes can cause human cancers, but has been lacking for genes implicated in generating aneuploidy. However, recently we identified mutations in the mitotic checkpoint gene BUB1B in an autosomal recessive condition characterized by mosaic aneuploidies and childhood cancers. This finding strongly suggests that aneuploidy is causally related to cancer development.
遗传性癌症易感性综合征对于识别参与致癌作用的基因和信号通路至关重要。与独特癌症表型共分离的先天性基因突变提供了基因在癌症中因果作用的确凿证据。这类证据在证明癌基因和肿瘤抑制基因可导致人类癌症方面一直起着核心作用,但对于与非整倍体产生相关的基因却一直缺乏此类证据。然而,最近我们在一种以镶嵌性非整倍体和儿童癌症为特征的常染色体隐性疾病中,发现了有丝分裂检查点基因BUB1B的突变。这一发现有力地表明,非整倍体与癌症发展存在因果关系。