Significant evidence for a heritable contribution to cancer predisposition: a review of cancer familiality by site

<p>Abstract</p> <p>Background/Aims</p> <p>Sound and rigorous well-established, and newly extended, methods for genetic epidemiological analysis were used to analyze population evidence for genetic contributions to risk for numerous common cancer sites in Utah. The Utah...

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Main Authors: Albright Frederick, Teerlink Craig, Werner Theresa L, Cannon-Albright Lisa A
Format: Article
Language:English
Published: BMC 2012-04-01
Series:BMC Cancer
Online Access:http://www.biomedcentral.com/1471-2407/12/138
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spelling doaj-b6aca7a43a8e42c69f9c922aa99b22ce2020-11-25T00:17:07ZengBMCBMC Cancer1471-24072012-04-0112113810.1186/1471-2407-12-138Significant evidence for a heritable contribution to cancer predisposition: a review of cancer familiality by siteAlbright FrederickTeerlink CraigWerner Theresa LCannon-Albright Lisa A<p>Abstract</p> <p>Background/Aims</p> <p>Sound and rigorous well-established, and newly extended, methods for genetic epidemiological analysis were used to analyze population evidence for genetic contributions to risk for numerous common cancer sites in Utah. The Utah Population Database (UPDB) has provided important illumination of the familial contribution to cancer risk by cancer site.</p> <p>Methods</p> <p>With over 15 years of new cancer data since the previous comprehensive familial cancer analysis, we tested for excess familial clustering using an expanded Genealogical Index of Familiality (dGIF) methodology that provides for a more informative, but conservative test for the existence of a genetic contribution to familial relatedness in cancer.</p> <p>Results</p> <p>Some new cancer sites have been analyzed for the first time, having achieved sufficiently large sample size with additions to the UPDB. This new analysis has identified 6 cancer sites with significant evidence for a heritable contribution to risk, including lip, chronic lymphocytic leukemia, thyroid, lung, prostate, and melanoma.</p> <p>Conclusions</p> <p>Both environmentally and genetically-based familial clustering have clinical significance, and these results support increased surveillance for cancer of the same sites among close relatives of affected individuals for many more cancers than are typically considered.</p> http://www.biomedcentral.com/1471-2407/12/138
collection DOAJ
language English
format Article
sources DOAJ
author Albright Frederick
Teerlink Craig
Werner Theresa L
Cannon-Albright Lisa A
spellingShingle Albright Frederick
Teerlink Craig
Werner Theresa L
Cannon-Albright Lisa A
Significant evidence for a heritable contribution to cancer predisposition: a review of cancer familiality by site
BMC Cancer
author_facet Albright Frederick
Teerlink Craig
Werner Theresa L
Cannon-Albright Lisa A
author_sort Albright Frederick
title Significant evidence for a heritable contribution to cancer predisposition: a review of cancer familiality by site
title_short Significant evidence for a heritable contribution to cancer predisposition: a review of cancer familiality by site
title_full Significant evidence for a heritable contribution to cancer predisposition: a review of cancer familiality by site
title_fullStr Significant evidence for a heritable contribution to cancer predisposition: a review of cancer familiality by site
title_full_unstemmed Significant evidence for a heritable contribution to cancer predisposition: a review of cancer familiality by site
title_sort significant evidence for a heritable contribution to cancer predisposition: a review of cancer familiality by site
publisher BMC
series BMC Cancer
issn 1471-2407
publishDate 2012-04-01
description <p>Abstract</p> <p>Background/Aims</p> <p>Sound and rigorous well-established, and newly extended, methods for genetic epidemiological analysis were used to analyze population evidence for genetic contributions to risk for numerous common cancer sites in Utah. The Utah Population Database (UPDB) has provided important illumination of the familial contribution to cancer risk by cancer site.</p> <p>Methods</p> <p>With over 15 years of new cancer data since the previous comprehensive familial cancer analysis, we tested for excess familial clustering using an expanded Genealogical Index of Familiality (dGIF) methodology that provides for a more informative, but conservative test for the existence of a genetic contribution to familial relatedness in cancer.</p> <p>Results</p> <p>Some new cancer sites have been analyzed for the first time, having achieved sufficiently large sample size with additions to the UPDB. This new analysis has identified 6 cancer sites with significant evidence for a heritable contribution to risk, including lip, chronic lymphocytic leukemia, thyroid, lung, prostate, and melanoma.</p> <p>Conclusions</p> <p>Both environmentally and genetically-based familial clustering have clinical significance, and these results support increased surveillance for cancer of the same sites among close relatives of affected individuals for many more cancers than are typically considered.</p>
url http://www.biomedcentral.com/1471-2407/12/138
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