TY - JOUR
T1 - Telomere length in blood cells and breast cancer risk
T2 - Investigations in two case-control studies
AU - Zheng, Yun Ling
AU - Ambrosone, Christine
AU - Byrne, Celia
AU - Davis, Warren
AU - Nesline, Mary
AU - McCann, Susan E.
N1 - Funding Information:
Acknowledgments We thank Katherine Meeker, Kenshata Wat-kins, Whitney Mcleod, and Christine Nagel for their assistance in study subject recruitment; Dingfeng Han for performing TQ-PCR for telomere length measurement; and Lenka Goldman for data preparation. We are indebted to the physicians of the Betty Lou Ourisman Breast Center of the LCCC and the physicians in the department of surgical oncology of the RPCI for their strong support of patient recruitment. We thank Dr. Alan Meeker of Johns Hopkins University for providing Telometer software and Dr. Richard Cawthon of University of Utah for sharing their latest real-time telomere PCR protocol. The Clinical Molecular Epidemiology Shared Resource at the LCCC provided services for questionnaire data entry for the LCCC study. This work was supported by Susan G. Komen for the Cure (BCTR 0600562 to Y.L.Z); the National Institutes of Health cancer center support grant (P30 CA51008 to LCCC and P30 CA016056 to RPCI) and DOD grant (DAMD17-03-1-0446) supports the control recruitment for the LCCC study.
PY - 2010/4
Y1 - 2010/4
N2 - Telomere dysfunction, which leads to genomic instability, is hypothesized to play a causal role in the development of breast cancer. However, the few epidemiologic studies that assessed the relationship between telomere length in blood cells and breast cancer risk have been inconsistent. We conducted two case-control studies to further understand the role of telomere length and breast cancer risk. Overall telomere lengths were measured by telomere quantitative fluorescent in situ hybridization (TQFISH) and telomere quantitative real-time PCR (TQ-PCR). The associations between telomere length in blood leukocytes and risk of breast cancer were examined in two breast cancer case-control studies that were conducted at Roswell Park Cancer Institute (RPCI) and Lombardi Comprehensive Cancer Center (LCCC). Using the 50th percentile value in controls as a cut point, women who had shorter telomere length were not at significantly increased risk of breast cancer compared with women who had longer telomere length in the RPCI study (odds ratio [OR] = 1.34, 95% confidence interval [CI] = 0.84-2.12), in the LCCC study (OR = 1.18, 95% CI = 0.73-1.91), or in the combined RPCI and LCCC studies (OR = 1.23, 95% CI = 0.89-1.71). There was no significant dose-response relationship across quartiles of telomere length and no significant difference when comparing women in the lowest to highest quartile of telomere length. Overall telomere length in blood leukocytes was not significantly associated with the risk of breast cancer.
AB - Telomere dysfunction, which leads to genomic instability, is hypothesized to play a causal role in the development of breast cancer. However, the few epidemiologic studies that assessed the relationship between telomere length in blood cells and breast cancer risk have been inconsistent. We conducted two case-control studies to further understand the role of telomere length and breast cancer risk. Overall telomere lengths were measured by telomere quantitative fluorescent in situ hybridization (TQFISH) and telomere quantitative real-time PCR (TQ-PCR). The associations between telomere length in blood leukocytes and risk of breast cancer were examined in two breast cancer case-control studies that were conducted at Roswell Park Cancer Institute (RPCI) and Lombardi Comprehensive Cancer Center (LCCC). Using the 50th percentile value in controls as a cut point, women who had shorter telomere length were not at significantly increased risk of breast cancer compared with women who had longer telomere length in the RPCI study (odds ratio [OR] = 1.34, 95% confidence interval [CI] = 0.84-2.12), in the LCCC study (OR = 1.18, 95% CI = 0.73-1.91), or in the combined RPCI and LCCC studies (OR = 1.23, 95% CI = 0.89-1.71). There was no significant dose-response relationship across quartiles of telomere length and no significant difference when comparing women in the lowest to highest quartile of telomere length. Overall telomere length in blood leukocytes was not significantly associated with the risk of breast cancer.
KW - Biomarkers
KW - Blood leukocytes
KW - Breast cancer
KW - Genetic susceptibility
KW - Telomere length
UR - http://www.scopus.com/inward/record.url?scp=77950858257&partnerID=8YFLogxK
U2 - 10.1007/s10549-009-0440-z
DO - 10.1007/s10549-009-0440-z
M3 - Article
C2 - 19543829
AN - SCOPUS:77950858257
SN - 0167-6806
VL - 120
SP - 769
EP - 775
JO - Breast Cancer Research and Treatment
JF - Breast Cancer Research and Treatment
IS - 3
ER -