Plasma Protein Carbonyls and Breast Cancer Risk in Sisters Discordant for Breast Cancer from the New York Site of the Breast Cancer Family Registry

被引:26
作者
Zipprich, Jennifer [1 ]
Terry, Mary Beth [2 ]
Liao, Yuyan [2 ]
Agrawal, Meenakshi [1 ]
Gurvich, Irina [1 ]
Senie, Ruby [2 ]
Santella, Regina M. [1 ]
机构
[1] Columbia Univ, Mailman Sch Publ Hlth, Dept Environm Hlth Sci, New York, NY 10032 USA
[2] Columbia Univ, Mailman Sch Publ Hlth, Dept Epidemiol, New York, NY 10032 USA
基金
美国国家环境保护局;
关键词
HORMONE REPLACEMENT THERAPY; TOTAL ANTIOXIDANT STATUS; OXIDATIVE DNA-DAMAGE; LIPID-PEROXIDATION; POSTMENOPAUSAL WOMEN; STRESS; ESTROGEN; DISEASE; MALONDIALDEHYDE; CARCINOGENESIS;
D O I
10.1158/0008-5472.CAN-08-3418
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Reactive oxygen species are important in the pathogenesis of many diseases, including breast cancer. Several population-based case-control studies have shown that various biomarkers of oxidative stress are associated with an increase in breast cancer risk. We selected sisters discordant for breast cancer (n = 645) from the New York site of the Breast Cancer Family Registry to explore factors that contribute to variation in plasma protein carbonyls, and to determine whether this biomarker is associated with an increase in breast cancer risk among those with a family history. Late age at menarche, hormone replacement therapy use, and Hispanic race were significantly associated with lower plasma protein carbonyl levels in unaffected sisters. Plasma protein carbonyls were associated with an increase in breast cancer risk [Q2 odds ratio (OR), 1.4; 95% confidence interval (0), 0.8-2.7; Q3 OR, 2.4; 95% CI, 1.1-4.9; Q4 OR, 1.9; 95% CI, 0.8-4.2], although not in a dose-dependent manner. These data suggest that oxidative damage is a risk factor for breast cancer in high-risk women. [Cancer Res 2009;69(7):2966-72]
引用
收藏
页码:2966 / 2972
页数:7
相关论文
共 45 条
[1]  
Apter D, 1996, EUR J CANCER PREV, V5, P476
[2]   The genetics and genomics of cancer [J].
Balmain, A ;
Gray, J ;
Ponder, B .
NATURE GENETICS, 2003, 33 (Suppl 3) :238-244
[3]   Serum lipid peroxides and total antioxidant status in postmenopausal women on hormone replacement therapy [J].
Bednarek-Tupikowska, G ;
Tupikowski, K ;
Bidzinska, B ;
Bohdanowicz-Pawlak, A ;
Antonowicz-Juchniewicz, J ;
Kosowska, B ;
Milewicz, A .
GYNECOLOGICAL ENDOCRINOLOGY, 2004, 19 (02) :57-63
[4]   Familial breast cancer: collaborative reanalysis of individual data from 52 epidemiological studies including 58 209 women with breast cancer and 101 986 women without the disease [J].
Beral, V ;
Bull, D ;
Doll, R ;
Peto, R ;
Reeves, G .
LANCET, 2001, 358 (9291) :1389-1399
[5]   Potential mechanisms of estrogen quinone carcinogenesis [J].
Bolton, Judy L. ;
Thatcher, Gregory R. J. .
CHEMICAL RESEARCH IN TOXICOLOGY, 2008, 21 (01) :93-101
[6]   Diet and genetic factors associated with iron status in middle-aged women [J].
Cade, JE ;
Moreton, JA ;
O'Hara, B ;
Greenwood, DC ;
Moor, J ;
Burley, VJ ;
Kukalizch, K ;
Bishop, DT ;
Worwood, M .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 2005, 82 (04) :813-820
[7]   Fat overload aggravates oxidative stress in patients with the metabolic syndrome [J].
Cardona, F. ;
Tunez, I. ;
Tasset, I. ;
Montilla, P. ;
Collantes, E. ;
Tinahones, F. J. .
EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 2008, 38 (07) :510-515
[8]   Mechanisms of disease - Estrogen and the risk of breast cancer [J].
Clemons, M ;
Goss, P .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (04) :276-285
[9]   Protein carbonyl groups as biomarkers of oxidative stress [J].
Dalle-Donne, I ;
Rossi, R ;
Giustarini, D ;
Milzani, A ;
Colombo, R .
CLINICA CHIMICA ACTA, 2003, 329 (1-2) :23-38
[10]   Degradation of oxidized proteins by the 20S proteasome [J].
Davies, KJA .
BIOCHIMIE, 2001, 83 (3-4) :301-310