Inactivation of hCDC4 can cause chromosomal instability

被引:460
作者
Rajagopalan, H
Jallepalli, PV
Rago, C
Velculescu, VE
Kinzler, KW
Vogelstein, B
Lengauer, C [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Sidney Kimmel Comprehens Canc Ctr, Baltimore, MD 21231 USA
[2] Mem Sloan Kettering Canc Ctr, Program Mol Biol, New York, NY 10021 USA
[3] Johns Hopkins Univ, Inst Med, Howard Hughes Med Inst, Baltimore, MD 21231 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1038/nature02313
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Aneuploidy, an abnormal chromosome number, has been recognized as a hallmark of human cancer for nearly a century(1); however, the mechanisms responsible for this abnormality have remained elusive. Here we report the identification of mutations in hCDC4 (also known as Fbw7 or Archipelago) in both human colorectal cancers and their precursor lesions. We show that genetic inactivation of hCDC4, by means of targeted disruption of the gene in karyotypically stable colorectal cancer cells, results in a striking phenotype associated with micronuclei and chromosomal instability. This phenotype can be traced to a defect in the execution of metaphase and subsequent transmission of chromosomes, and is dependent on cyclin E-a protein that is regulated by hCDC4 (refs 2-4). Our data suggest that chromosomal instability is caused by specific genetic alterations in a large fraction of human cancers and can occur before malignant conversion.
引用
收藏
页码:77 / 81
页数:5
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