Metals and Breast Cancer

被引:166
作者
Byrne, Celia [1 ]
Divekar, Shailaja D. [2 ,3 ,4 ]
Storchan, Geoffrey B. [2 ,3 ,4 ]
Parodi, Daniela A. [2 ,3 ,4 ]
Martin, Mary Beth [5 ,6 ,7 ]
机构
[1] Uniformed Serv Univ Hlth Sci, Bethesda, MD 20814 USA
[2] Georgetown Univ, Dept Oncol, Lombardi Comprehens Canc Ctr, Washington, DC 20007 USA
[3] Georgetown Univ, Dept Biochem, Lombardi Comprehens Canc Ctr, Washington, DC 20007 USA
[4] Georgetown Univ, Dept Mol & Cellular Biol, Lombardi Comprehens Canc Ctr, Washington, DC 20007 USA
[5] Dept Oncol, Washington, DC USA
[6] Dept Biochem, Washington, DC USA
[7] Dept Mol & Cellular Biol, Washington, DC USA
关键词
Estrogens; Estrogen receptor; Metalloestrogens; Metals; Endocrine disruptors; Breast cancer; ESTROGEN-RECEPTOR-ALPHA; LIGAND-BINDING DOMAIN; TOTAL DIET SAMPLES; ER-ALPHA; CADMIUM EXPOSURE; CELL-PROLIFERATION; SIGNALING PATHWAYS; STEROID-RECEPTORS; CRYSTAL-STRUCTURE; IN-VIVO;
D O I
10.1007/s10911-013-9273-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Metalloestrogens are metals that activate the estrogen receptor in the absence of estradiol. The metalloestrogens fall into two subclasses: metal/metalloid anions and bivalent cationic metals. The metal/metalloid anions include compounds such as arsenite, nitrite, selenite, and vanadate while the bivalent cations include metals such as cadmium, calcium, cobalt, copper, nickel, chromium, lead, mercury, and tin. The best studied metalloestrogen is cadmium. It is a heavy metal and a prevalent environmental contaminant with no known physiological function. This review addresses our current understanding of the mechanism by which cadmium and the bivalent cationic metals activate estrogen receptor-alpha. The review also summarizes the in vitro and in vivo evidence that cadmium functions as an estrogen and the potential role of cadmium in breast cancer.
引用
收藏
页码:63 / 73
页数:11
相关论文
共 116 条
[1]   Long-term dietary cadmium intake and postmenopausal endometrial cancer incidence:: A population-based prospective cohort study [J].
Akesson, Agneta ;
Julin, Bettina ;
Wolk, Alicja .
CANCER RESEARCH, 2008, 68 (15) :6435-6441
[2]   SOLUTION STRUCTURE OF (CD2+)(1)-CALBINDIN D-9K REVEALS DETAILS OF THE STEPWISE STRUCTURAL-CHANGES ALONG THE APO-](CA2+)(1)(II)-](CA2+)(2)(I,II) BINDING PATHWAY [J].
AKKE, M ;
FORSEN, S ;
CHAZIN, WJ .
JOURNAL OF MOLECULAR BIOLOGY, 1995, 252 (01) :102-121
[3]   Cadmium-Induced Effects on Cellular Signaling Pathways in the Liver of Transgenic Estrogen Reporter Mice [J].
Ali, Imran ;
Damdimopoulou, Pauliina ;
Stenius, Ulla ;
Adamsson, Annika ;
Makela, Sari I. ;
Akesson, Agneta ;
Berglund, Marika ;
Hakansson, Helen ;
Halldin, Krister .
TOXICOLOGICAL SCIENCES, 2012, 127 (01) :66-75
[4]   Estrogen-Like Effects of Cadmium in Vivo Do Not Appear to be Mediated via the Classical Estrogen Receptor Transcriptional Pathway [J].
Ali, Imran ;
Penttinen-Damdimopoulou, Pauliina E. ;
Makela, Sari I. ;
Berglund, Marika ;
Stenius, Ulla ;
Akesson, Agneta ;
Hakansson, Helen ;
Halldin, Krister .
ENVIRONMENTAL HEALTH PERSPECTIVES, 2010, 118 (10) :1389-1394
[5]   MODULATION OF TRANSCRIPTIONAL ACTIVATION BY LIGAND-DEPENDENT PHOSPHORYLATION OF THE HUMAN ESTROGEN RECEPTOR-A/B REGION [J].
ALI, S ;
METZGER, D ;
BORNERT, JM ;
CHAMBON, P .
EMBO JOURNAL, 1993, 12 (03) :1153-1160
[6]   Melatonin prevents the estrogenic effects of sub-chronic administration of cadmium on mice mammary glands and uterus [J].
Alonso-Gonzalez, C. ;
Gonzalez, A. ;
Mazarrasa, O. ;
Guezmes, A. ;
Sanchez-Mateos, S. ;
Martinez-Campa, C. ;
Cos, S. ;
Sanchez-Barcelo, E. J. ;
Mediavilla, M. D. .
JOURNAL OF PINEAL RESEARCH, 2007, 42 (04) :403-410
[7]  
[Anonymous], 1980, IARC MON EV CARC RIS, V23
[8]  
[Anonymous], 1976, CADM NICK SOM EXP MI
[9]  
[Anonymous], 1984, HLTH ASS DOC CHROM
[10]  
[Anonymous], 1995, NICK