Influence of arsenate and arsenite on signal transduction pathways: an update

被引:90
作者
Druwe, Ingrid L. [1 ]
Vaillancourt, Richard R. [1 ]
机构
[1] Univ Arizona, Coll Pharm, Dept Pharmacol & Toxicol, Tucson, AZ 85721 USA
关键词
Arsenic; Arsenite; Arsenate; Signal transduction; INDUCED MALIGNANT-TRANSFORMATION; HUMAN BLADDER CELLS; PROSTATE EPITHELIAL-CELLS; KAPPA-B ACTIVATION; PROTEIN-KINASE-B; MONOMETHYLARSONOUS ACID; OXIDATIVE STRESS; DRINKING-WATER; INDUCED APOPTOSIS; DNA METHYLATION;
D O I
10.1007/s00204-010-0554-4
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Arsenic has been a recognized contaminant and toxicant, as well as a medicinal compound throughout human history. Populations throughout the world are exposed to arsenic and these exposures have been associated with a number of human cancers. Not much is known about the role of arsenic as a human carcinogen and more recently its role in non-cancerous diseases, such as cardiovascular disease, hypertension and diabetes mellitus have been uncovered. The health effects associated with arsenic are numerous and the association between arsenic exposure and human disease has intensified the search for molecular mechanisms that describe the biological activity of arsenic in humans and leads to the aforementioned disease states. Arsenic poses a human health risk due in part to the regulation of cellular signal transduction pathways and over the last few decades, some cellular mechanisms that account for arsenic toxicity, as well as, signal transduction pathways have been discovered. However, given the ubiquitous nature of arsenic in the environment, making sense of all the data remains a challenge. This review will focus on our knowledge of signal transduction pathways that are regulated by arsenic.
引用
收藏
页码:585 / 596
页数:12
相关论文
共 91 条
[1]   Inorganic arsenite-induced malignant transformation of human prostate epithelial cells [J].
Achanzar, WE ;
Brambila, EM ;
Diwan, BA ;
Webber, MM ;
Waalkes, MP .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2002, 94 (24) :1888-1891
[2]   Characterization of a 3-phosphoinositide-dependent protein kinase which phosphorylates and activates protein kinase B alpha [J].
Alessi, DR ;
James, SR ;
Downes, CP ;
Holmes, AB ;
Gaffney, PRJ ;
Reese, CB ;
Cohen, P .
CURRENT BIOLOGY, 1997, 7 (04) :261-269
[3]  
[Anonymous], EPIDEMIOLOGY
[4]   Molecular events associated with arsenic-induced malignant transformation of human prostatic epithelial cells: aberrant genomic DNA methylation and K-ras oncogene activation [J].
Benbrahim-Tallaa, L ;
Waterland, RA ;
Styblo, M ;
Achanzar, WE ;
Webber, MM ;
Waalkes, MP .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2005, 206 (03) :288-298
[5]   Mechanisms of acquired androgen independence during arsenic-induced malignant transformation of human prostate epithelial cells [J].
Benbrahim-Tallaa, Lamia ;
Webber, Mukta M. ;
Waalkes, Michael P. .
ENVIRONMENTAL HEALTH PERSPECTIVES, 2007, 115 (02) :243-247
[6]   ARSENATE RESISTANT MUTANTS OF ESCHERICHIA-COLI AND PHOSPHATE TRANSPORT [J].
BENNETT, RL ;
MALAMY, MH .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1970, 40 (02) :496-&
[7]   Differences in malignant melanoma between children and adolescents - A 35-year epidemiological study [J].
Berg, P ;
Lindelof, B .
ARCHIVES OF DERMATOLOGY, 1997, 133 (03) :295-297
[8]   DNA methylation patterns and epigenetic memory [J].
Bird, A .
GENES & DEVELOPMENT, 2002, 16 (01) :6-21
[9]   Monomethylarsonous acid induces transformation of human bladder cells [J].
Bredfeldt, Tiffany G. ;
Jagadish, Bhumasamudram ;
Eblin, Kylee E. ;
Mash, Eugene A. ;
Gandolfi, A. Jay .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2006, 216 (01) :69-79
[10]   Two new genes, PHO86 and PHO87, involved in inorganic phosphate uptake in Saccharomyces cerevisiae [J].
BunYa, M ;
Shikata, K ;
Nakade, S ;
Yompakdee, C ;
Harashima, S ;
Oshima, Y .
CURRENT GENETICS, 1996, 29 (04) :344-351