Runs of homozygosity and a cluster of vulvar cancer in young Australian Aboriginal women

被引:13
作者
McWhirter, Rebekah E. [1 ,2 ]
Thomson, Russell J. [2 ]
Marthick, James R. [2 ]
Rumbold, Alice R. [3 ]
Brown, Matthew A. [4 ]
Taylor-Thomson, Debbie [1 ]
Maypilama, Elaine L. [1 ]
Condon, John R. [1 ]
Dickinson, Joanne L. [1 ,2 ]
机构
[1] Charles Darwin Univ, Menzies Sch Hlth Res, Casuarina, NT 0811, Australia
[2] Univ Tasmania, Menzies Res Inst Tasmania, Hobart, Tas 7000, Australia
[3] Univ Adelaide, Adelaide, SA 5005, Australia
[4] Univ Queensland, Princess Alexandra Hosp, Translat Res Inst, Diamantina Inst, Woolloongabba, Qld 4102, Australia
基金
澳大利亚研究理事会; 英国医学研究理事会;
关键词
Vulvar cancer; Vulvar intraepithelial neoplasia; Homozygosity; Human papillomavirus; Genetic risk factors; Aboriginal and Torres Strait Islander peoples; HUMAN-PAPILLOMAVIRUS; INTRAEPITHELIAL NEOPLASIA; RISK; AUTOZYGOSITY; ASSOCIATION; COMMUNITIES; LESIONS; TRENDS;
D O I
10.1016/j.ygyno.2014.03.566
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective. A cluster of vulvar cancer exists in young Aboriginal women living in remote communities in Arnhem Land, Australia. A genetic case-control study was undertaken involving 30 cases of invasive vulvar cancer and its precursor lesion, high-grade vulvar intraepithelial neoplasia (VIN), and 61 controls, matched for age and community of residence. It was hypothesized that this small, isolated population may exhibit increased autozygosity, implicating recessive effects as a possible mechanism for increased susceptibility to vulvar cancer. Methods. Genotyping data from saliva samples were used to identify runs of homozygosity (ROH) in order to calculate estimates of genome-wide homozygosity. Results. No evidence of an effect of genome-wide homozygosity on vulvar cancer and VIN in East Arnhem women was found, nor was any individual ROH found to be significantly associated with case status. This study found further evidence supporting an association between previous diagnosis of CIN and diagnosis of vulvar cancer or VIN, but found no association with any other medical history variable. Conclusions. These findings do not eliminate the possibility of genetic risk factors being involved in this cancer cluster, but rather suggest that alternative analytical strategies and genetic models should be explored. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:421 / 426
页数:6
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