Identification of rare germline copy number variations over-represented in five human cancer types
Park, Richard W
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CitationPark, Richard W, Tae-Min Kim, Simon Kasif, and Peter J Park. 2015. “Identification of rare germline copy number variations over-represented in five human cancer types.” Molecular Cancer 14 (1): 25. doi:10.1186/s12943-015-0292-6. http://dx.doi.org/10.1186/s12943-015-0292-6.
AbstractBackground: Copy number variations (CNVs) are increasingly recognized as significant disease susceptibility markers in many complex disorders including cancer. The availability of a large number of chromosomal copy number profiles in both malignant and normal tissues in cancer patients presents an opportunity to characterize not only somatic alterations but also germline CNVs, which may confer increased risk for cancer. Results: We explored the germline CNVs in five cancer cohorts from the Cancer Genome Atlas (TCGA) consisting of 351 brain, 336 breast, 342 colorectal, 370 renal, and 314 ovarian cancers, genotyped on Affymetrix SNP6.0 arrays. Comparing these to ~3000 normal controls from another study, our case–control association study revealed 39 genomic loci (9 brain, 3 breast, 4 colorectal, 11 renal, and 12 ovarian cancers) as potential candidates of tumor susceptibility loci. Many of these loci are new and in some cases are associated with a substantial increase in disease risk. The majority of the observed loci do not overlap with coding sequences; however, several observed genomic loci overlap with known cancer genes including RET in brain cancers, ERBB2 in renal cell carcinomas, and DCC in ovarian cancers, all of which have not been previously associated with germline changes in cancer. Conclusions: This large-scale genome-wide association study for CNVs across multiple cancer types identified several novel rare germline CNVs as cancer predisposing genomic loci. These loci can potentially serve as clinically useful markers conferring increased cancer risk. Electronic supplementary material The online version of this article (doi:10.1186/s12943-015-0292-6) contains supplementary material, which is available to authorized users.
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