Ethnic Background and Genetic Variation in the Evaluation of Cancer Risk: A Systematic Review

被引:60
|
作者
Jing, Lijun [1 ]
Su, Li [2 ]
Ring, Brian Z. [1 ]
机构
[1] Huazhong Univ Sci & Technol, Coll Life Sci & Technol, Inst Genom & Personalized Med, Wuhan 430074, Hubei, Peoples R China
[2] Huazhong Univ Sci & Technol, Coll Life Sci & Technol, Minist Educ, Key Lab Mol Biophys, Wuhan 430074, Hubei, Peoples R China
来源
PLOS ONE | 2014年 / 9卷 / 06期
关键词
GENOME-WIDE ASSOCIATION; BREAST-CANCER; PROSTATE-CANCER; LUNG-CANCER; COLORECTAL-CANCER; POPULATION STRATIFICATION; HEPATOCELLULAR-CARCINOMA; RACIAL-DIFFERENCES; GASTRIC-CANCER; POLYMORPHISM;
D O I
10.1371/journal.pone.0097522
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
The clinical use of genetic variation in the evaluation of cancer risk is expanding, and thus understanding how determinants of cancer susceptibility identified in one population can be applied to another is of growing importance. However there is considerable debate on the relevance of ethnic background in clinical genetics, reflecting both the significance and complexity of genetic heritage. We address this via a systematic review of reported associations with cancer risk for 82 markers in 68 studies across six different cancer types, comparing association results between ethnic groups and examining linkage disequilibrium between risk alleles and nearby genetic loci. We find that the relevance of ethnic background depends on the question. If asked whether the association of variants with disease risk is conserved across ethnic boundaries, we find that the answer is yes, the majority of markers show insignificant variability in association with cancer risk across ethnic groups. However if the question is whether a significant association between a variant and cancer risk is likely to reproduce, the answer is no, most markers do not validate in an ethnic group other than the discovery cohort's ancestry. This lack of reproducibility is not attributable to studies being inadequately populated due to low allele frequency in other ethnic groups. Instead, differences in local genomic structure between ethnic groups are associated with the strength of association with cancer risk and therefore confound interpretation of the implied physiologic association tracked by the disease allele. This suggest that a biological association for cancer risk alleles may be broadly consistent across ethnic boundaries, but reproduction of a clinical study in another ethnic group is uncommon, in part due to confounding genomic architecture. As clinical studies are increasingly performed globally this has important implications for how cancer risk stratifiers should be studied and employed.
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页数:11
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