Telomere length shows no association with BRCA1 and BRCA2 mutation status

dc.contributor.author
Killick, Emma
dc.contributor.author
Tymrakiewicz, Malgorzata
dc.contributor.author
Cieza-Borrella, Clara
dc.contributor.author
Smith, Paula
dc.contributor.author
Thompson, Deborah J.
dc.contributor.author
Pooley, Karen A.
dc.contributor.author
Easton, Douglas F.
dc.contributor.author
Bancroft, Elizabeth K.
dc.contributor.author
Page, Elizabeth
dc.contributor.author
Leongamornlert, Daniel
dc.contributor.author
IMPACT Study Collaborators
dc.contributor.author
Kote-Jarai, Zsofia
dc.contributor.author
Eeles, Rosalind A.
dc.contributor.author
Blanco Guillermo, Ignacio
dc.contributor.author
Salinas Masdeu, Mònica
dc.date.issued
2018-01-29T11:55:15Z
dc.date.issued
2018-01-29T11:55:15Z
dc.date.issued
2014-01-29
dc.date.issued
2018-01-29T11:55:15Z
dc.identifier
1932-6203
dc.identifier
https://hdl.handle.net/2445/119372
dc.identifier
642411
dc.identifier
24489760
dc.description.abstract
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.
dc.format
6 p.
dc.format
application/pdf
dc.language
eng
dc.publisher
Public Library of Science (PLoS)
dc.relation
Reproducció del document publicat a: https://doi.org/10.1371/journal.pone.0086659
dc.relation
PLoS One, 2014, vol. 9, num. 1, p. e86659
dc.relation
https://doi.org/10.1371/journal.pone.0086659
dc.relation
info:eu-repo/grantAgreement/EC/FP7/223175/EU//COGS
dc.rights
cc-by (c) Killick, Emma et al., 2014
dc.rights
http://creativecommons.org/licenses/by/3.0/es
dc.rights
info:eu-repo/semantics/openAccess
dc.source
Articles publicats en revistes (Patologia i Terapèutica Experimental)
dc.subject
Telòmer
dc.subject
Proteïnes supressores de tumors
dc.subject
Mutació (Biologia)
dc.subject
Tumors
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Càncer de mama
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Càncer de pròstata
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Telomere
dc.subject
Tumor suppressor protein
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Mutation (Biology)
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Tumors
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Breast cancer
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Prostate cancer
dc.title
Telomere length shows no association with BRCA1 and BRCA2 mutation status
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/publishedVersion


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