Literature DB >> 18375840

The signatures of autozygosity among patients with colorectal cancer.

Manny D Bacolod1, Gunter S Schemmann, Shuang Wang, Richard Shattock, Sarah F Giardina, Zhaoshi Zeng, Jinru Shia, Robert F Stengel, Norman Gerry, Josephine Hoh, Tomas Kirchhoff, Bert Gold, Michael F Christman, Kenneth Offit, William L Gerald, Daniel A Notterman, Jurg Ott, Philip B Paty, Francis Barany.   

Abstract

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 (>or=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.

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Year:  2008        PMID: 18375840      PMCID: PMC4383032          DOI: 10.1158/0008-5472.CAN-07-5250

Source DB:  PubMed          Journal:  Cancer Res        ISSN: 0008-5472            Impact factor:   12.701


  47 in total

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Review 4.  The genetic epidemiology of cancer: interpreting family and twin studies and their implications for molecular genetic approaches.

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5.  Principal components analysis corrects for stratification in genome-wide association studies.

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  28 in total

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2.  Identification of novel candidate genes for Alzheimer's disease by autozygosity mapping using genome wide SNP data.

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3.  Array-based karyotyping for prognostic assessment in chronic lymphocytic leukemia: performance comparison of Affymetrix 10K2.0, 250K Nsp, and SNP6.0 arrays.

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Review 4.  Molecular profiling of colon tumors: the search for clinically relevant biomarkers of progression, prognosis, therapeutics, and predisposition.

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5.  Relationship between Deleterious Variation, Genomic Autozygosity, and Disease Risk: Insights from The 1000 Genomes Project.

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Review 6.  Genetic diversity, inbreeding and cancer.

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7.  Genome-wide autozygosity mapping in human populations.

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9.  An integrated Bayesian analysis of LOH and copy number data.

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10.  Association of survival and disease progression with chromosomal instability: a genomic exploration of colorectal cancer.

Authors:  Michal Sheffer; Manny D Bacolod; Or Zuk; Sarah F Giardina; Hanna Pincas; Francis Barany; Philip B Paty; William L Gerald; Daniel A Notterman; Eytan Domany
Journal:  Proc Natl Acad Sci U S A       Date:  2009-04-09       Impact factor: 11.205

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