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Complex Segregation Analysis of Pedigrees from the Gilda Radner Familial Ovarian Cancer Registry Reveals Evidence for Mendelian Dominant Inheritance

BACKGROUND: Familial component is estimated to account for about 10% of ovarian cancer. However, the mode of inheritance of ovarian cancer remains poorly understood. The goal of this study was to investigate the inheritance model that best fits the observed transmission pattern of ovarian cancer amo...

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Autores principales: Tayo, Bamidele O., DiCioccio, Richard A., Liang, Yulan, Trevisan, Maurizio, Cooper, Richard S., Lele, Shashikant, Sucheston, Lara, Piver, Steven M., Odunsi, Kunle
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2694280/
https://www.ncbi.nlm.nih.gov/pubmed/19536330
http://dx.doi.org/10.1371/journal.pone.0005939
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author Tayo, Bamidele O.
DiCioccio, Richard A.
Liang, Yulan
Trevisan, Maurizio
Cooper, Richard S.
Lele, Shashikant
Sucheston, Lara
Piver, Steven M.
Odunsi, Kunle
author_facet Tayo, Bamidele O.
DiCioccio, Richard A.
Liang, Yulan
Trevisan, Maurizio
Cooper, Richard S.
Lele, Shashikant
Sucheston, Lara
Piver, Steven M.
Odunsi, Kunle
author_sort Tayo, Bamidele O.
collection PubMed
description BACKGROUND: Familial component is estimated to account for about 10% of ovarian cancer. However, the mode of inheritance of ovarian cancer remains poorly understood. The goal of this study was to investigate the inheritance model that best fits the observed transmission pattern of ovarian cancer among 7669 members of 1919 pedigrees ascertained through probands from the Gilda Radner Familial Ovarian Cancer Registry at Roswell Park Cancer Institute, Buffalo, New York. METHODOLOGY/PRINCIPAL FINDINGS: Using the Statistical Analysis for Genetic Epidemiology program, we carried out complex segregation analyses of ovarian cancer affection status by fitting different genetic hypothesis-based regressive multivariate logistic models. We evaluated the likelihood of sporadic, major gene, environmental, general, and six types of Mendelian models. Under each hypothesized model, we also estimated the susceptibility allele frequency, transmission probabilities for the susceptibility allele, baseline susceptibility and estimates of familial association. Comparisons between models were carried out using either maximum likelihood ratio test in the case of hierarchical models, or Akaike information criterion for non-nested models. When assessed against sporadic model without familial association, the model with both parent-offspring and sib-sib residual association could not be rejected. Likewise, the Mendelian dominant model that included familial residual association provided the best-fitting for the inheritance of ovarian cancer. The estimated disease allele frequency in the dominant model was 0.21. CONCLUSIONS/SIGNIFICANCE: This report provides support for a genetic role in susceptibility to ovarian cancer with a major autosomal dominant component. This model does not preclude the possibility of polygenic inheritance of combined effects of multiple low penetrance susceptibility alleles segregating dominantly.
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spelling pubmed-26942802009-06-16 Complex Segregation Analysis of Pedigrees from the Gilda Radner Familial Ovarian Cancer Registry Reveals Evidence for Mendelian Dominant Inheritance Tayo, Bamidele O. DiCioccio, Richard A. Liang, Yulan Trevisan, Maurizio Cooper, Richard S. Lele, Shashikant Sucheston, Lara Piver, Steven M. Odunsi, Kunle PLoS One Research Article BACKGROUND: Familial component is estimated to account for about 10% of ovarian cancer. However, the mode of inheritance of ovarian cancer remains poorly understood. The goal of this study was to investigate the inheritance model that best fits the observed transmission pattern of ovarian cancer among 7669 members of 1919 pedigrees ascertained through probands from the Gilda Radner Familial Ovarian Cancer Registry at Roswell Park Cancer Institute, Buffalo, New York. METHODOLOGY/PRINCIPAL FINDINGS: Using the Statistical Analysis for Genetic Epidemiology program, we carried out complex segregation analyses of ovarian cancer affection status by fitting different genetic hypothesis-based regressive multivariate logistic models. We evaluated the likelihood of sporadic, major gene, environmental, general, and six types of Mendelian models. Under each hypothesized model, we also estimated the susceptibility allele frequency, transmission probabilities for the susceptibility allele, baseline susceptibility and estimates of familial association. Comparisons between models were carried out using either maximum likelihood ratio test in the case of hierarchical models, or Akaike information criterion for non-nested models. When assessed against sporadic model without familial association, the model with both parent-offspring and sib-sib residual association could not be rejected. Likewise, the Mendelian dominant model that included familial residual association provided the best-fitting for the inheritance of ovarian cancer. The estimated disease allele frequency in the dominant model was 0.21. CONCLUSIONS/SIGNIFICANCE: This report provides support for a genetic role in susceptibility to ovarian cancer with a major autosomal dominant component. This model does not preclude the possibility of polygenic inheritance of combined effects of multiple low penetrance susceptibility alleles segregating dominantly. Public Library of Science 2009-06-17 /pmc/articles/PMC2694280/ /pubmed/19536330 http://dx.doi.org/10.1371/journal.pone.0005939 Text en Tayo et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Tayo, Bamidele O.
DiCioccio, Richard A.
Liang, Yulan
Trevisan, Maurizio
Cooper, Richard S.
Lele, Shashikant
Sucheston, Lara
Piver, Steven M.
Odunsi, Kunle
Complex Segregation Analysis of Pedigrees from the Gilda Radner Familial Ovarian Cancer Registry Reveals Evidence for Mendelian Dominant Inheritance
title Complex Segregation Analysis of Pedigrees from the Gilda Radner Familial Ovarian Cancer Registry Reveals Evidence for Mendelian Dominant Inheritance
title_full Complex Segregation Analysis of Pedigrees from the Gilda Radner Familial Ovarian Cancer Registry Reveals Evidence for Mendelian Dominant Inheritance
title_fullStr Complex Segregation Analysis of Pedigrees from the Gilda Radner Familial Ovarian Cancer Registry Reveals Evidence for Mendelian Dominant Inheritance
title_full_unstemmed Complex Segregation Analysis of Pedigrees from the Gilda Radner Familial Ovarian Cancer Registry Reveals Evidence for Mendelian Dominant Inheritance
title_short Complex Segregation Analysis of Pedigrees from the Gilda Radner Familial Ovarian Cancer Registry Reveals Evidence for Mendelian Dominant Inheritance
title_sort complex segregation analysis of pedigrees from the gilda radner familial ovarian cancer registry reveals evidence for mendelian dominant inheritance
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2694280/
https://www.ncbi.nlm.nih.gov/pubmed/19536330
http://dx.doi.org/10.1371/journal.pone.0005939
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