Importance of xeroderma pigmentosum group D polymorphisms in susceptibility to ovarian cancer

被引:17
作者
Costa, Sandra [1 ]
Pinto, Daniela
Pereira, Deolinda
Vasconcelos, Andre
Afonso-Lopes, Carlos
Osorio, Teresa
Lopes, Carlos
Medeiros, Rui
机构
[1] Univ Minho, ICVS, Life & Hlth Sci Res Inst, Hlth Sci Sch, P-4710057 Braga, Portugal
[2] Inst Portugues Oncol Francisco Gentil, Mol Oncol Dept Pathol, P-4200072 Oporto, Portugal
[3] Inst Portugues Oncol Francisco Gentil, Dept Med Oncol, P-4200072 Oporto, Portugal
[4] Inst Portugues Oncol Francisco Gentil, Dept Gynecol, P-4200072 Oporto, Portugal
[5] Abel Salazar Inst Biomed Sci, ICBAS, P-4099003 Oporto, Portugal
关键词
XPD; NER; DNA repair; ovarian cancer; polymorphisms;
D O I
10.1016/j.canlet.2006.03.014
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The purpose of this study was to evaluate the role of XPD genotypes as genetic indicator of susceptibility to ovarian cancer. We have used a case-control study. We analysed DNA samples from 141 ovarian cancer patients and 202 control subjects, for three XPD polymorphisms using PCR-RFLP. We observed that Asn312Asn XPD genotype carriers have increased susceptibility of ovarian cancer (OR = 2.46 95% CI 1.20-5.06; P = 0.015). Furthermore, we found that carriers of Gln751Gln XPD genotype have an increased susceptibility of ovarian cancer (OR = 3.40 95% CI 1.61-7.15; P = 0.001). Asn312Asn and Gln751Gln are particularly associated with an early-stage of disease. Our results suggest an important role for Asn312Asn and Gln751Gln XPD polymorphisms in the susceptibility to ovarian cancer. (c) 2006 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:324 / 330
页数:7
相关论文
共 49 条
[1]   Functional characterization of Polymorphisms in DNA repair genes using cytogenetic challenge assays [J].
Au, WW ;
Salama, SA ;
Sierra-Torres, CH .
ENVIRONMENTAL HEALTH PERSPECTIVES, 2003, 111 (15) :1843-1850
[2]   XPD gene polymorphism and host characteristics in the association with cutaneous malignant melanoma risk [J].
Baccarelli, A ;
Calista, D ;
Minghetti, P ;
Marinelli, B ;
Albetti, B ;
Tseng, T ;
Hedayati, M ;
Grossman, L ;
Landi, G ;
Struewing, JP ;
Landi, MT .
BRITISH JOURNAL OF CANCER, 2004, 90 (02) :497-502
[3]   Variability in nucleotide excision repair and cancer risk: a review [J].
Benhamou, S ;
Sarasin, A .
MUTATION RESEARCH-REVIEWS IN MUTATION RESEARCH, 2000, 462 (2-3) :149-158
[4]   Loss of heterozygosity in human ovarian cancer on chromosome 19q [J].
Bicher, A ;
Ault, K ;
Kimmelman, A ;
Gershenson, D ;
Reed, E ;
Liang, B .
GYNECOLOGIC ONCOLOGY, 1997, 66 (01) :36-40
[5]   Genetic polymorphisms in DNA repair genes and risk of lung cancer [J].
Butkiewicz, D ;
Rusin, M ;
Enewold, L ;
Shields, PG ;
Chorazy, M ;
Harris, CC .
CARCINOGENESIS, 2001, 22 (04) :593-597
[6]   Catechol ortho-quinones: the electrophilic compounds that form depurinating DNA adducts and could initiate cancer and other diseases [J].
Cavalieri, EL ;
Li, KM ;
Balu, N ;
Saeed, M ;
Devanesan, P ;
Higginbotham, S ;
Zhao, J ;
Gross, ML ;
Rogan, EG .
CARCINOGENESIS, 2002, 23 (06) :1071-1077
[7]   DNA repair gene XRCC1 and XPD polymorphisms and risk of lung cancer in a Chinese population [J].
Chen, SQ ;
Tang, DL ;
Xue, KX ;
Xu, L ;
Ma, GJ ;
Hsu, YZ ;
Cho, SS .
CARCINOGENESIS, 2002, 23 (08) :1321-1325
[8]   Mutations in the XPD helicase gene result in XP and TTD phenotypes, preventing interaction between XPD and the p44 subunit of TFIIH [J].
Coin, F ;
Marinoni, JC ;
Rodolfo, C ;
Fribourg, S ;
Pedrini, AM ;
Egly, JM .
NATURE GENETICS, 1998, 20 (02) :184-188
[9]   ERCC1 AND ERCC2 EXPRESSION IN MALIGNANT-TISSUES FROM OVARIAN-CANCER PATIENTS [J].
DABHOLKAR, M ;
BOSTICKBRUTON, F ;
WEBER, C ;
BOHR, VA ;
EGWUAGU, C ;
REED, E .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1992, 84 (19) :1512-1517
[10]  
GALLI MC, 1981, CANCER-AM CANCER SOC, V47, P1297, DOI 10.1002/1097-0142(19810315)47:6<1297::AID-CNCR2820470611>3.0.CO