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      Prevalence and Penetrance of Major Genes and Polygenes for Colorectal Cancer

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          Abstract

          <div class="section"> <a class="named-anchor" id="S1"> <!-- named anchor --> </a> <h5 class="section-title" id="d6845513e355">Background</h5> <p id="P1">While high-risk mutations in identified major susceptibility genes (DNA mismatch repair genes and <i>MUTYH</i>) account for some familial aggregation of colorectal cancer, their population prevalence and the causes of the remaining familial aggregation are not known. </p> </div><div class="section"> <a class="named-anchor" id="S2"> <!-- named anchor --> </a> <h5 class="section-title" id="d6845513e363">Methods</h5> <p id="P2">We studied the families of 5,744 colorectal cancer cases (probands) recruited from population cancer registries in the USA, Canada and Australia and screened probands for mutations in mismatch repair genes and <i>MUTYH</i>. We conducted modified segregation analyses using the cancer history of first-degree relatives, conditional on the proband’s age at diagnosis. We estimated the prevalence of mutations in the identified genes, the prevalence of and hazard ratio for unidentified major gene mutations, and the variance of the residual polygenic component. </p> </div><div class="section"> <a class="named-anchor" id="S3"> <!-- named anchor --> </a> <h5 class="section-title" id="d6845513e371">Results</h5> <p id="P3">We estimated that 1 in 279 of the population carry mutations in mismatch repair genes ( <i>MLH1</i>= 1 in 1946, <i>MSH2</i>= 1 in 2841, <i>MSH6</i>= 1 in 758, <i>PMS2</i>= 1 in 714), 1 in 45 carry mutations in <i>MUTYH</i>, and 1 in 504 carry mutations associated with an average 31-fold increased risk of colorectal cancer in unidentified major genes. The estimated polygenic variance was reduced by 30–50% after allowing for unidentified major genes and decreased from 3.3 for age &lt;40 years to 0.5 for age ≥70 years (equivalent to sibling relative risks of 5.1 to 1.3, respectively). </p> </div><div class="section"> <a class="named-anchor" id="S4"> <!-- named anchor --> </a> <h5 class="section-title" id="d6845513e391">Conclusion</h5> <p id="P4">Unidentified major genes might explain one-third to one-half of the missing heritability of colorectal cancer. </p> </div><div class="section"> <a class="named-anchor" id="S5"> <!-- named anchor --> </a> <h5 class="section-title" id="d6845513e396">Impact</h5> <p id="P5">Our findings could aid gene discovery and development of better colorectal cancer risk prediction models. </p> </div>

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          Author and article information

          Journal
          Cancer Epidemiology Biomarkers & Prevention
          Cancer Epidemiol Biomarkers Prev
          American Association for Cancer Research (AACR)
          1055-9965
          1538-7755
          March 01 2017
          March 2017
          October 31 2016
          : 26
          : 3
          : 404-412
          Article
          10.1158/1055-9965.EPI-16-0693
          5336409
          27799157
          233f59bd-7e3d-4897-a952-9d1e8ccdaeb4
          © 2016
          History

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