Activation of the DNA damage checkpoint and genomic instability in human precancerous lesions

被引:0
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作者
Vassilis G. Gorgoulis
Leandros-Vassilios F. Vassiliou
Panagiotis Karakaidos
Panayotis Zacharatos
Athanassios Kotsinas
Triantafillos Liloglou
Monica Venere
Richard A. DiTullio
Nikolaos G. Kastrinakis
Brynn Levy
Dimitris Kletsas
Akihiro Yoneta
Meenhard Herlyn
Christos Kittas
Thanos D. Halazonetis
机构
[1] School of Medicine,Department of Histology and Embryology
[2] University of Athens,Roy Castle Lung Cancer Research Programme
[3] Cancer Research Center,Department of Pathology and Laboratory Medicine
[4] University of Liverpool,Department of Human Genetics
[5] The Wistar Institute,Institute of Biology
[6] Graduate Group in Biomedical Sciences,undefined
[7] University of Pennsylvania,undefined
[8] Mount Sinai School of Medicine,undefined
[9] National Centre of Scientific Research ‘Demokritos’,undefined
来源
Nature | 2005年 / 434卷
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摘要
Two groups this week report findings that could have a big impact on our view of cancer development. Both looked at tumours (bladder, breast and colorectal, and in lung and skin) in various stages of progression for signs of a DNA damage response. And both find that early stages of cancer development are associated with an active DNA damage response and p53-dependent cell death. This suggests that the induction of a DNA damage response by oncogenic events is a potent tumour suppression mechanism, and explains the selective pressure for p53 mutations in precancerous lesions. Importantly, activation of the DNA damage checkpoint occurs before chromosome instability and malignancy. On the cover, 53BP1 foci in lung hyperplasia (green indicates DNA damage checkpoint activation).
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页码:907 / 913
页数:6
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