Genetic ancestry is associated with colorectal adenomas and adenocarcinomas in Latino populations

被引:17
作者
Hernandez-Suarez, Gustavo [1 ,2 ]
Carolina Sanabria, Maria [1 ,3 ]
Serrano, Marta [1 ,3 ]
Herran, Oscar F. [4 ]
Perez, Jesus [5 ]
Plata, Jose L. [6 ]
Zabaleta, Jovanny [7 ,8 ]
Tenesa, Albert [2 ,9 ]
机构
[1] Inst Nacl Cancerol Colombia, Grp Invest Epidemiol, Bogota, Colombia
[2] Univ Edinburgh, Roslin Inst, Edinburgh, Midlothian, Scotland
[3] Univ Nacl Colombia, Dept Quim, Cundinamarca, Colombia
[4] Univ Ind Santander, Fac Med, Bucaramanga, Colombia
[5] Univ Libre, Fac Med, Barranquilla, Colombia
[6] Fdn Oftalmol Santander, Bucaramanga, Colombia
[7] Louisiana State Univ, Hlth Sci Ctr, Dept Pediat, New Orleans, LA USA
[8] Louisiana State Univ, Hlth Sci Ctr, Stanley S Scott Canc Ctr, New Orleans, LA USA
[9] Univ Edinburgh, MRC Human Genet Unit MRC IGMM, Edinburgh, Midlothian, Scotland
基金
英国生物技术与生命科学研究理事会;
关键词
colorectal neoplasm; pedigree; polymorphism; genetic; Latin America; Colombia; CANCER; RISK; ADMIXTURE; INFERENCE; MARKERS; POLYPS; COLON; DIET;
D O I
10.1038/ejhg.2013.310
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Colorectal cancer rates in Latin American countries are less than half of those observed in the United States. Latin Americans are the resultant of generations of an admixture of Native American, European, and African individuals. The potential role of genetic admixture in colorectal carcinogenesis has not been examined. We evaluate the association of genetic ancestry with colorectal neoplasms in 190 adenocarcinomas, 113 sporadic adenomas and 243 age- and sex-matched controls enrolled in a multicentric case control study in Colombia. Individual ancestral genetic fractions were estimated using the STRUCTURE software, based on allele frequencies and assuming three distinct population origins. We used the Illumina Cancer Panel to genotype 1,421 sparse single-nucleotide polymorphisms (SNPs), and Northern and Western European ancestry, LWJ and Han Chinese in Beijing, China populations from the HapMap project as references. A total of 678 autosomal SNPs overlapped with the HapMap data set SNPs and were used for ancestry estimations. African mean ancestry fraction was higher in adenomas (0.13, 95% confidence interval (95% CI)=0.11-0.15) and cancer cases (0.14, 95% CI =0.12-0.16) compared with controls (0.11, 95% CI =0.10-0.12). Conditional logistic regression analysis, controlling for known risk factors, showed a positive association of African ancestry per 10% increase with both colorectal adenoma (odds ratio (OR)=1.12, 95% CI =0.97-1.30) and adenocarcinoma (OR =1.19, 95% CI =1.05-1.35). In conclusion, increased African ancestry (or variants linked to it) contributes to the increased susceptibility of colorectal cancer in admixed Latin American population.
引用
收藏
页码:1208 / 1216
页数:9
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