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Telomere Length Shows No Association with BRCA1 and BRCA2 Mutation Status

This study aimed to determine whether telomere length (TL) is a marker of cancer risk or genetic status amongst two cohorts of BRCA1 and BRCA2 mutation carriers and controls. The first group was a prospective set of 665 male BRCA1/2 mutation carriers and controls (mean age 53 years), all healthy at...

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Autores principales: Killick, Emma, Tymrakiewicz, Malgorzata, Cieza-Borrella, Clara, Smith, Paula, Thompson, Deborah J., Pooley, Karen A., Easton, Doug F., Bancroft, Elizabeth, Page, Elizabeth, Leongamornlert, Daniel, Kote-Jarai, Zsofia, Eeles, Rosalind A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3906069/
https://www.ncbi.nlm.nih.gov/pubmed/24489760
http://dx.doi.org/10.1371/journal.pone.0086659
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author Killick, Emma
Tymrakiewicz, Malgorzata
Cieza-Borrella, Clara
Smith, Paula
Thompson, Deborah J.
Pooley, Karen A.
Easton, Doug F.
Bancroft, Elizabeth
Page, Elizabeth
Leongamornlert, Daniel
Kote-Jarai, Zsofia
Eeles, Rosalind A.
author_facet Killick, Emma
Tymrakiewicz, Malgorzata
Cieza-Borrella, Clara
Smith, Paula
Thompson, Deborah J.
Pooley, Karen A.
Easton, Doug F.
Bancroft, Elizabeth
Page, Elizabeth
Leongamornlert, Daniel
Kote-Jarai, Zsofia
Eeles, Rosalind A.
author_sort Killick, Emma
collection PubMed
description This study aimed to determine whether telomere length (TL) is a marker of cancer risk or genetic status amongst two cohorts of BRCA1 and BRCA2 mutation carriers and controls. The first group was a prospective set of 665 male BRCA1/2 mutation carriers and controls (mean age 53 years), all healthy at time of enrolment and blood donation, 21 of whom have developed prostate cancer whilst on study. The second group consisted of 283 female BRCA1/2 mutation carriers and controls (mean age 48 years), half of whom had been diagnosed with breast cancer prior to enrolment. TL was quantified by qPCR from DNA extracted from peripheral blood lymphocytes. Weighted and unweighted Cox regressions and linear regression analyses were used to assess whether TL was associated with BRCA1/2 mutation status or cancer risk. We found no evidence for association between developing cancer or being a BRCA1 or BRCA2 mutation carrier and telomere length. It is the first study investigating TL in a cohort of genetically predisposed males and although TL and BRCA status was previously studied in females our results don't support the previous finding of association between hereditary breast cancer and shorter TL.
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spelling pubmed-39060692014-01-31 Telomere Length Shows No Association with BRCA1 and BRCA2 Mutation Status Killick, Emma Tymrakiewicz, Malgorzata Cieza-Borrella, Clara Smith, Paula Thompson, Deborah J. Pooley, Karen A. Easton, Doug F. Bancroft, Elizabeth Page, Elizabeth Leongamornlert, Daniel Kote-Jarai, Zsofia Eeles, Rosalind A. PLoS One Research Article This study aimed to determine whether telomere length (TL) is a marker of cancer risk or genetic status amongst two cohorts of BRCA1 and BRCA2 mutation carriers and controls. The first group was a prospective set of 665 male BRCA1/2 mutation carriers and controls (mean age 53 years), all healthy at time of enrolment and blood donation, 21 of whom have developed prostate cancer whilst on study. The second group consisted of 283 female BRCA1/2 mutation carriers and controls (mean age 48 years), half of whom had been diagnosed with breast cancer prior to enrolment. TL was quantified by qPCR from DNA extracted from peripheral blood lymphocytes. Weighted and unweighted Cox regressions and linear regression analyses were used to assess whether TL was associated with BRCA1/2 mutation status or cancer risk. We found no evidence for association between developing cancer or being a BRCA1 or BRCA2 mutation carrier and telomere length. It is the first study investigating TL in a cohort of genetically predisposed males and although TL and BRCA status was previously studied in females our results don't support the previous finding of association between hereditary breast cancer and shorter TL. Public Library of Science 2014-01-29 /pmc/articles/PMC3906069/ /pubmed/24489760 http://dx.doi.org/10.1371/journal.pone.0086659 Text en © 2014 Killick 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
Killick, Emma
Tymrakiewicz, Malgorzata
Cieza-Borrella, Clara
Smith, Paula
Thompson, Deborah J.
Pooley, Karen A.
Easton, Doug F.
Bancroft, Elizabeth
Page, Elizabeth
Leongamornlert, Daniel
Kote-Jarai, Zsofia
Eeles, Rosalind A.
Telomere Length Shows No Association with BRCA1 and BRCA2 Mutation Status
title Telomere Length Shows No Association with BRCA1 and BRCA2 Mutation Status
title_full Telomere Length Shows No Association with BRCA1 and BRCA2 Mutation Status
title_fullStr Telomere Length Shows No Association with BRCA1 and BRCA2 Mutation Status
title_full_unstemmed Telomere Length Shows No Association with BRCA1 and BRCA2 Mutation Status
title_short Telomere Length Shows No Association with BRCA1 and BRCA2 Mutation Status
title_sort telomere length shows no association with brca1 and brca2 mutation status
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3906069/
https://www.ncbi.nlm.nih.gov/pubmed/24489760
http://dx.doi.org/10.1371/journal.pone.0086659
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