The signatures of autozygosity among patients with colorectal cancer

Manny D. Bacolod, 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

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43 Scopus citations


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.

Original languageEnglish (US)
Pages (from-to)2610-2621
Number of pages12
JournalCancer Research
Issue number8
StatePublished - Apr 15 2008

All Science Journal Classification (ASJC) codes

  • Oncology
  • Cancer Research


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