Jump to main content
US EPA
United States Environmental Protection Agency
Search
Search
Main menu
Environmental Topics
Laws & Regulations
About EPA
Health & Environmental Research Online (HERO)
Contact Us
Print
Feedback
Export to File
Search:
This record has one attached file:
Add More Files
Attach File(s):
Display Name for File*:
Save
Citation
Tags
HERO ID
200497
Reference Type
Journal Article
Title
Carcinogenicity and chronic toxicity in rats and mice exposed by inhalation to 1,2-dichloroethane for two years
Author(s)
Nagano, K; Umeda, Y; Senoh, H; Gotoh, K; Arito, H; Yamamoto, S; Matsushima, T
Year
2006
Is Peer Reviewed?
Yes
Journal
Journal of Occupational Health
ISSN:
1341-9145
EISSN:
1348-9585
Volume
48
Issue
6
Page Numbers
424-436
Language
English
PMID
17179635
DOI
10.1539/joh.48.424
Web of Science Id
WOS:000242870100003
URL
https://www.proquest.com/scholarly-journals/carcinogenicity-chronic-toxicity-rats-mice/docview/68265978/se-2
Exit
Relationship(s)
uses data from
012636
Inhalation carcinogenesis studies of six halogenated hydrocarbons in rats and mice
Abstract
Carcinogenicity and chronic toxicity of 1,2-dichloroethane (DCE) were examined by inhalation exposure of groups of 50 F344 rats and 50 BDF1 mice of both sexes to DCE vapor or clean air as control for 6 h/d, 5 d/wk and 104 wk. The rats were exposed to 10, 40 or 160 ppm (v/v) DCE, while the mice were exposed to 10, 30 or 90 ppm. The 2-yr exposure to DCE produced a dose-dependent increase in incidences of benign and malignant tumors, including subcutaneous fibroma, mammary gland fibroadenoma and peritoneal mesothelioma in male rats; subcutaneous fibroma and mammary gland adenoma, fibroadenoma and adenocarcinoma in female rats; and bronchiolo-alveolar adenoma and carcinoma, endometrial stromal polyp, mammary gland adenocarcinoma and hepatocellular adenoma in female mice. No exposure-related change in the incidence of non-neoplastic lesions or in any hematological, blood biochemical or urinary parameter occurred in any DCE-exposed rat or mouse group. The types of tumors and their target organs found in this study were consistent with those observed in rats and mice administered DCE by gavage in a NCI study. Selection of the exposure concentrations was considered appropriate with reference to the maximum tolerated dose for the highest doses and an occupational exposure limit of DCE for the lowest dose. The present findings suggest that those carcinogenic responses be primarily considered for standard setting of occupational and environmental exposure to DCE
Keywords
Adenoma; blood; Environmental Exposure; Female; Incidence; Male; Mice; Occupational Exposure; Rats; toxicity
Tags
IRIS
•
Chloroform Combined (current)
•
Tetrachloroethylene (Perc) (Final, 2012)
•
OPPT_N-methylpyrrolidone (NMP)_F. Human Health
•
OPPT_Perchloroethylene (Perc)_C. Engineering
•
OPPT_Perchloroethylene (Perc)_D. Exposure
•
OPPT_Perchloroethylene (Perc)_E. Fate
•
OPPT_Perchloroethylene (Perc)_F. Human Health
Home
Learn about HERO
Using HERO
Search HERO
Projects in HERO
Risk Assessment
Transparency & Integrity