Telomere length shows no association with BRCA1 and BRCA2 mutation status

dc.contributor.authorKillick, Emma
dc.contributor.authorTymrakiewicz, Malgorzata
dc.contributor.authorCieza-Borrella, Clara
dc.contributor.authorSmith, Paula
dc.contributor.authorThompson, Deborah J.
dc.contributor.authorPooley, Karen A.
dc.contributor.authorEaston, Douglas F.
dc.contributor.authorBancroft, Elizabeth K.
dc.contributor.authorPage, Elizabeth
dc.contributor.authorLeongamornlert, Daniel
dc.contributor.authorIMPACT Study Collaborators
dc.contributor.authorKote-Jarai, Zsofia
dc.contributor.authorEeles, Rosalind A.
dc.contributor.authorBlanco Guillermo, Ignacio
dc.contributor.authorSalinas Masdeu, Mònica
dc.date.accessioned2018-01-29T11:55:15Z
dc.date.available2018-01-29T11:55:15Z
dc.date.issued2014-01-29
dc.date.updated2018-01-29T11:55:15Z
dc.description.abstractThis 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.extent6 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec642411
dc.identifier.issn1932-6203
dc.identifier.pmid24489760
dc.identifier.urihttps://hdl.handle.net/2445/119372
dc.language.isoeng
dc.publisherPublic Library of Science (PLoS)
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1371/journal.pone.0086659
dc.relation.ispartofPLoS One, 2014, vol. 9, num. 1, p. e86659
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/FP7/223175/EU//COGS
dc.relation.urihttps://doi.org/10.1371/journal.pone.0086659
dc.rightscc-by (c) Killick, Emma et al., 2014
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es
dc.sourceArticles publicats en revistes (Patologia i Terapèutica Experimental)
dc.subject.classificationTelòmer
dc.subject.classificationProteïnes supressores de tumors
dc.subject.classificationMutació (Biologia)
dc.subject.classificationTumors
dc.subject.classificationCàncer de mama
dc.subject.classificationCàncer de pròstata
dc.subject.otherTelomere
dc.subject.otherTumor suppressor protein
dc.subject.otherMutation (Biology)
dc.subject.otherTumors
dc.subject.otherBreast cancer
dc.subject.otherProstate cancer
dc.titleTelomere length shows no association with BRCA1 and BRCA2 mutation status
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

Fitxers

Paquet original

Mostrant 1 - 1 de 1
Carregant...
Miniatura
Nom:
642411.pdf
Mida:
229.04 KB
Format:
Adobe Portable Document Format