Cancer in xeroderma pigmentosum and related disorders of DNA repair

被引:309
作者
Cleaver, JE [1 ]
机构
[1] Univ Calif San Francisco, Auerback Melanoma Lab, UCSF Canc Ctr, San Francisco, CA 94143 USA
关键词
D O I
10.1038/nrc1652
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Nucleotide- excision repair diseases exhibit cancer, complex developmental disorders and neurodegeneration. Cancer is the hallmark of xeroderma pigmentosum ( XP), and neurodegeneration and developmental disorders are the hallmarks of Cockayne syndrome and trichothiodystrophy. A distinguishing feature is that the DNA-repair or DNA- replication deficiencies of XP involve most of the genome, whereas the defects in CS are confined to actively transcribed genes. Many of the proteins involved in repair are also components of dynamic multiprotein complexes, transcription factors, ubiquitylation cofactors and signal- transduction networks. Complex clinical phenotypes might therefore result from unanticipated effects on other genes and proteins.
引用
收藏
页码:564 / 573
页数:11
相关论文
共 162 条
[1]   Centrosome protein centrin 2/caltractin 1 is part of the xeroderma pigmentosum group C complex that initiates global genome nucleotide excision repair [J].
Araki, M ;
Masutani, C ;
Takemura, M ;
Uchida, A ;
Sugasawa, K ;
Kondoh, J ;
Ohkuma, Y ;
Hanaoka, F .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (22) :18665-18672
[2]   Oxidative damage-induced PCNA complex formation is efficient in xeroderma pigmentosum group A but reduced in Cockayne syndrome group B cells [J].
Balajee, AS ;
Dianova, I ;
Bohr, VA .
NUCLEIC ACIDS RESEARCH, 1999, 27 (22) :4476-4482
[3]   EVIDENCE FOR DEFECTIVE REPAIR OF CYCLOBUTANE PYRIMIDINE DIMERS WITH NORMAL REPAIR OF OTHER DNA PHOTOPRODUCTS IN A TRANSCRIPTIONALLY ACTIVE GENE TRANSFECTED INTO COCKAYNE SYNDROME CELLS [J].
BARRETT, SF ;
ROBBINS, JH ;
TARONE, RE ;
KRAEMER, KH .
MUTATION RESEARCH, 1991, 255 (03) :281-291
[4]   Damage recognition in nucleotide excision repair of DNA [J].
Batty, DP ;
Wood, RD .
GENE, 2000, 241 (02) :193-204
[5]   The CSB protein actively wraps DNA [J].
Beerens, N ;
Hoeijmakers, JHJ ;
Kanaar, R ;
Vermeulen, W ;
Wyman, C .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (06) :4722-4729
[6]  
Berg RJW, 2000, CANCER RES, V60, P2858
[7]  
Berg RJW, 1997, CANCER RES, V57, P581
[8]   STRUCTURE AND FUNCTION OF TELOMERES [J].
BLACKBURN, EH .
NATURE, 1991, 350 (6319) :569-573
[9]   High levels of patched gene mutations in basal-cell carcinomas from patients with xeroderma pigmentosum [J].
Bodak, N ;
Queille, S ;
Avril, MF ;
Bouadjar, B ;
Drougard, C ;
Sarasin, A ;
Daya-Grosjean, L .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (09) :5117-5122
[10]   A comparative analysis of transcribed genes in the mouse hypothalamus and neocortex reveals chromosomal clustering [J].
Boon, WM ;
Beissbarth, T ;
Hyde, L ;
Smyth, G ;
Gunnersen, J ;
Denton, DA ;
Scott, H ;
Tan, SS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (41) :14972-14977