TY - JOUR
T1 - Telomere length shows no association with BRCA1 and BRCA2 mutation status
AU - Evans, Gareth
AU - Killick, Emma
AU - Tymrakiewicz, Malgorzata
AU - Cieza-Borrella, Clara
AU - Smith, Paula
AU - Thompson, Deborah J.
AU - Pooley, Karen A.
AU - Easton, Doug F.
AU - Bancroft, Elizabeth
AU - Page, Elizabeth
AU - Leongamornlert, Daniel
AU - Kote-Jarai, Zsofia
AU - Eeles, Rosalind A.
N1 - 13232, Cancer Research UK, United Kingdom15007, Cancer Research UK, United KingdomP30 CA016520, NCI NIH HHS, United States
PY - 2014/1/29
Y1 - 2014/1/29
N2 - 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. © 2014 Killick et al.
AB - 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. © 2014 Killick et al.
UR - https://www.scopus.com/pages/publications/84900422907
U2 - 10.1371/journal.pone.0086659
DO - 10.1371/journal.pone.0086659
M3 - Article
C2 - 24489760
VL - 9
JO - PLoS ONE
JF - PLoS ONE
IS - 1
M1 - e86659
ER -