Toxicity and carcinogenicity of chromium compounds in humans

被引:700
作者
Costa, M [1 ]
Klein, CB [1 ]
机构
[1] NYU, Sch Med, Dept Environm Med, New York, NY 10016 USA
关键词
carcinogenesis risk assessment; chromium; drinking water; skin cancer; uptake;
D O I
10.1080/10408440500534032
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Chromium is a human carcinogen primarily by inhalation exposure in occupational settings. Although lung cancer has been established as a consequence of hexavalent chromium exposure in smokers and nonsmokers, some cancers of other tissues of the gastrointestinal and central nervous systems have also been noted. Except for a few reports from China, little is known about the health risks of environmental exposures to chromium. Likewise, there has been a lack of epidemiological studies of human exposure to hexavalent Cr by drinking water or ingestion, and it has been suggested that humans can perhaps tolerate hexavalent Cr at higher levels than the current drinking water standard of 50 ppb. This review highlights the most recent data on the induction of skin tumors in mice by chronic drinking-water exposure to hexavalent chromium in combination with solar ultraviolet light. This experimental system represents an important new animal model for chromate-induced cancers by ingestion of drinking water, and it suggests by extrapolation that chromate can likely be considered a human carcinogen by ingestion as well. The potential use of this animal model for future risk assessment is discussed.
引用
收藏
页码:155 / 163
页数:9
相关论文
共 67 条
[41]   Human health risk and exposure assessment of chromium (VI) in tap water [J].
Paustenbach, DJ ;
Finley, BL ;
Mowat, FS ;
Kerger, BD .
JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH-PART A-CURRENT ISSUES, 2003, 66 (14) :1295-1339
[42]   METABOLIC REDUCTION OF CHROMIUM AS A THRESHOLD MECHANISM LIMITING ITS INVIVO ACTIVITY [J].
PETRILLI, FL ;
DEFLORA, S .
SCIENCE OF THE TOTAL ENVIRONMENT, 1988, 71 (03) :357-364
[43]   Is hexavalent chromium carcinogenic via ingestion? A weight-of-evidence review [J].
Proctor, DM ;
Otani, JM ;
Finley, BL ;
Paustenbach, DJ ;
Bland, JA ;
Speizer, N ;
Sargent, EV .
JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH-PART A-CURRENT ISSUES, 2002, 65 (10) :701-746
[44]   Absence of toxic effects in F344/N rats and B6C3F1 mice following subchronic administration of chromium picolinate monohydrate [J].
Rhodes, MC ;
Hébert, CD ;
Herbert, RA ;
Morinello, EJ ;
Roycroft, JH ;
Travlos, GS ;
Abdo, KM .
FOOD AND CHEMICAL TOXICOLOGY, 2005, 43 (01) :21-29
[45]   ANALYSIS OF THE BINDING-SITES OF CHROMIUM TO DNA AND PROTEIN INVITRO AND IN INTACT-CELLS [J].
SALNIKOW, K ;
ZHITKOVICH, A ;
COSTA, M .
CARCINOGENESIS, 1992, 13 (12) :2341-2346
[46]   REACTION OF CR(VI) WITH ASCORBATE AND HYDROGEN-PEROXIDE GENERATES HYDROXYL RADICALS AND CAUSES DNA-DAMAGE - ROLE OF A CR(IV)-MEDIATED FENTON-LIKE REACTION [J].
SHI, XL ;
MAO, Y ;
KNAPTON, AD ;
DING, M ;
ROJANASAKUL, Y ;
GANNETT, PM ;
DALAL, N ;
LIU, KJ .
CARCINOGENESIS, 1994, 15 (11) :2475-2478
[47]   DEFEROXAMINE INHIBITION OF CR(V)-MEDIATED RADICAL GENERATION AND DEOXYGUANINE HYDROXYLATION - ESR AND HPLC EVIDENCE [J].
SHI, XL ;
SUN, XY ;
GANNETT, PM ;
DALAL, NS .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1992, 293 (02) :281-286
[48]   Lack of mutagenicity of chromium picolinate in the hypoxanthine phosphoribosyltransferase gene mutation assay in Chinese hamster ovary cells [J].
Slesinski, RS ;
Clarke, JJ ;
San, RHC ;
Gudi, R .
MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS, 2005, 585 (1-2) :86-95
[49]  
SUGIYAMA M, 1986, MOL PHARMACOL, V29, P606
[50]   ROLE OF PHYSIOLOGICAL ANTIOXIDANTS IN CHROMIUM(VI)-INDUCED CELLULAR INJURY [J].
SUGIYAMA, M .
FREE RADICAL BIOLOGY AND MEDICINE, 1992, 12 (05) :397-407