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Molecular Biology, Pathobiology, and Genetics |
1 Department of Microbiology, Weill Medical College of Cornell University; 2 Department of Biostatistics, Mailman School of Public Health, Columbia University; Departments of 3 Surgery, 4 Pathology, and 5 Medicine, Memorial Sloan-Kettering Cancer Center; 6 Laboratory of Statistical Genetics, Rockefeller University, New York, New York; 7 School of Engineering and Applied Science and 8 Department of Molecular Biology, Princeton University, Princeton, New Jersey; 9 Laboratory of Genomic Diversity, National Cancer Institute at Frederick, Frederick, Maryland; 10 Department of Genetics and Genomics, Boston University, Boston, Massachusetts; and 11 School of Public Health, Yale University, New Haven, Connecticut
Requests for reprints: Francis Barany, Department of Microbiology and Immunology, Cornell University Weill Medical College, New York, NY 10021. Phone: 212-746-6509; Fax: 212-746-7983; E-mail: barany{at}med.cornell.edu.
Key Words: Colorectal cancer • Identity by Descent • Autozygosity • SNP Array • Jewish • Ashkenazi
Previous studies have shown that among populations with a high rate of consanguinity, there is a significant increase in the prevalence of cancer. Single nucleotide polymorphism (SNP) array data (Affymetrix, 50K XbaI) analysis revealed long regions of homozygosity in genomic DNAs taken from tumor and matched normal tissues of colorectal cancer (CRC) patients. The presence of these regions in the genome may indicate levels of consanguinity in the individual's family lineage. We refer to these autozygous regions as identity-by-descent (IBD) segments. In this study, we compared IBD segments in 74 mostly Caucasian CRC patients (mean age of 66 years) to two control data sets: (a) 146 Caucasian individuals (mean age of 80 years) who participated in an age-related macular degeneration (AMD) study and (b) 118 cancer-free Caucasian individuals from the Framingham Heart Study (mean age of 67 years). Our results show that the percentage of CRC patients with IBD segments (
4 Mb length and 50 SNPs probed) in the genome is at least twice as high as the AMD or Framingham control groups. Also, the average length of these IBD regions in the CRC patients is more than twice the length of the two control data sets. Compared with control groups, IBD segments are found to be more common among individuals of Jewish background. We believe that these IBD segments within CRC patients are likely to harbor important CRC-related genes with low-penetrance SNPs and/or mutations, and, indeed, two recently identified CRC predisposition SNPs in the 8q24 region were confirmed to be homozygous in one particular patient carrying an IBD segment covering the region. [Cancer Res 2008;68(8):2610–21]
This article has been cited by other articles:
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  M. Sheffer, M. D. Bacolod, O. Zuk, S. F. Giardina, H. Pincas, F. Barany, P. B. Paty, W. L. Gerald, D. A. Notterman, and E. Domany Association of survival and disease progression with chromosomal instability: A genomic exploration of colorectal cancer PNAS, April 28, 2009; 106(17): 7131 - 7136. [Abstract] [Full Text] [PDF]
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 M. D. Bacolod, G. S. Schemmann, S. F. Giardina, P. Paty, D. A. Notterman, and F. Barany Emerging Paradigms in Cancer Genetics: Some Important Findings from High-Density Single Nucleotide Polymorphism Array Studies Cancer Res., February 1, 2009; 69(3): 723 - 727. [Abstract] [Full Text] [PDF]
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 C. Eng, G. Assie, and T. LaFramboise Germline Genomic Homozygosity and Cancer Risk--Reply JAMA, July 9, 2008; 300(2): 170 - 170. [Full Text] [PDF]
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