Evaluation of Diuron (3-[3,4-dichlorophenyl]-1,1-dimethyl urea) in a Two-stage Mouse Skin Carcinogenesis Assay

Detalhes bibliográficos
Autor(a) principal: Ferrucio, Bianca [UNESP]
Data de Publicação: 2010
Outros Autores: da Silva Franchi, Carla Adriene [UNESP], Boldrin, Natalia Ferreira [UNESP], Oliveira, Maria Luiza Cotrim Sartor de [UNESP], Camargo, João Lauro Viana de [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1177/0192623310375452
http://hdl.handle.net/11449/13004
Resumo: Diuron (3-[3,4-dichlorophenyl]-1,1-dimethyl urea) is an herbicide with carcinogenic activity in rats and mice, which have developed respectively urothelial and mammary gland tumors in long-term studies. Accordingly, diuron has been categorized as a "likely human carcinogen" by the U. S. Environmental Protection Agency. Although the carcinogenesis-initiating activity of diuron has been reported in an early initiation-promotion mouse skin study, its genotoxic potential has been disputed. It is necessary to clarify the mode of action through which it has caused rodent neoplasia and verify its relevance to humans. Herein, two experiments were developed to verify the initiating and promoting potentials of diuron in a twenty-three-and a twenty-one-week-long mouse skin carcinogenesis protocol. In one, dimethylsulfoxide (DMSO) was the solvent for the herbicide; in the other, acetone was the alternative solvent in order to verify whether DMSO had inhibitory influence on a potential cutaneous carcinogenic activity. The adopted schedule for the tumor-promoting agent 12-O-tetradecanoylphorbol 13-acetate (TPA) resulted in skin ulcers, which demonstrates the need for careful selection of TPA dose levels and frequency of application in this model. In both studies, diuron did not exert any influence on the skin carcinogenesis process, in contrast with results already reported in the literature.
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spelling Evaluation of Diuron (3-[3,4-dichlorophenyl]-1,1-dimethyl urea) in a Two-stage Mouse Skin Carcinogenesis Assaydiuron (3-[3; 4-dichlorophenyl]-; 1-dimethyl urea)skin carcinogenesisinitiation-promotionDMSOTPADiuron (3-[3,4-dichlorophenyl]-1,1-dimethyl urea) is an herbicide with carcinogenic activity in rats and mice, which have developed respectively urothelial and mammary gland tumors in long-term studies. Accordingly, diuron has been categorized as a "likely human carcinogen" by the U. S. Environmental Protection Agency. Although the carcinogenesis-initiating activity of diuron has been reported in an early initiation-promotion mouse skin study, its genotoxic potential has been disputed. It is necessary to clarify the mode of action through which it has caused rodent neoplasia and verify its relevance to humans. Herein, two experiments were developed to verify the initiating and promoting potentials of diuron in a twenty-three-and a twenty-one-week-long mouse skin carcinogenesis protocol. In one, dimethylsulfoxide (DMSO) was the solvent for the herbicide; in the other, acetone was the alternative solvent in order to verify whether DMSO had inhibitory influence on a potential cutaneous carcinogenic activity. The adopted schedule for the tumor-promoting agent 12-O-tetradecanoylphorbol 13-acetate (TPA) resulted in skin ulcers, which demonstrates the need for careful selection of TPA dose levels and frequency of application in this model. In both studies, diuron did not exert any influence on the skin carcinogenesis process, in contrast with results already reported in the literature.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)São Paulo State Univ, UNESP, Ctr Evaluat Environm Impact Human Hlth TOXICAM, Dept Pathol,Botucatu Med Sch, São Paulo, BrazilSão Paulo State Univ, UNESP, Ctr Evaluat Environm Impact Human Hlth TOXICAM, Dept Pathol,Botucatu Med Sch, São Paulo, BrazilFAPESP: 06/60506-1FAPESP: 06/04630-5FAPESP: 08/01809-0Sage Publications IncUniversidade Estadual Paulista (Unesp)Ferrucio, Bianca [UNESP]da Silva Franchi, Carla Adriene [UNESP]Boldrin, Natalia Ferreira [UNESP]Oliveira, Maria Luiza Cotrim Sartor de [UNESP]Camargo, João Lauro Viana de [UNESP]2014-05-20T13:37:32Z2014-05-20T13:37:32Z2010-08-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article756-764http://dx.doi.org/10.1177/0192623310375452Toxicologic Pathology. Thousand Oaks: Sage Publications Inc, v. 38, n. 5, p. 756-764, 2010.0192-6233http://hdl.handle.net/11449/1300410.1177/0192623310375452WOS:000286314800009Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengToxicologic Pathology1.9660,807info:eu-repo/semantics/openAccess2024-09-03T13:15:29Zoai:repositorio.unesp.br:11449/13004Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-09-03T13:15:29Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Evaluation of Diuron (3-[3,4-dichlorophenyl]-1,1-dimethyl urea) in a Two-stage Mouse Skin Carcinogenesis Assay
title Evaluation of Diuron (3-[3,4-dichlorophenyl]-1,1-dimethyl urea) in a Two-stage Mouse Skin Carcinogenesis Assay
spellingShingle Evaluation of Diuron (3-[3,4-dichlorophenyl]-1,1-dimethyl urea) in a Two-stage Mouse Skin Carcinogenesis Assay
Ferrucio, Bianca [UNESP]
diuron (3-[3; 4-dichlorophenyl]-; 1-dimethyl urea)
skin carcinogenesis
initiation-promotion
DMSO
TPA
title_short Evaluation of Diuron (3-[3,4-dichlorophenyl]-1,1-dimethyl urea) in a Two-stage Mouse Skin Carcinogenesis Assay
title_full Evaluation of Diuron (3-[3,4-dichlorophenyl]-1,1-dimethyl urea) in a Two-stage Mouse Skin Carcinogenesis Assay
title_fullStr Evaluation of Diuron (3-[3,4-dichlorophenyl]-1,1-dimethyl urea) in a Two-stage Mouse Skin Carcinogenesis Assay
title_full_unstemmed Evaluation of Diuron (3-[3,4-dichlorophenyl]-1,1-dimethyl urea) in a Two-stage Mouse Skin Carcinogenesis Assay
title_sort Evaluation of Diuron (3-[3,4-dichlorophenyl]-1,1-dimethyl urea) in a Two-stage Mouse Skin Carcinogenesis Assay
author Ferrucio, Bianca [UNESP]
author_facet Ferrucio, Bianca [UNESP]
da Silva Franchi, Carla Adriene [UNESP]
Boldrin, Natalia Ferreira [UNESP]
Oliveira, Maria Luiza Cotrim Sartor de [UNESP]
Camargo, João Lauro Viana de [UNESP]
author_role author
author2 da Silva Franchi, Carla Adriene [UNESP]
Boldrin, Natalia Ferreira [UNESP]
Oliveira, Maria Luiza Cotrim Sartor de [UNESP]
Camargo, João Lauro Viana de [UNESP]
author2_role author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Ferrucio, Bianca [UNESP]
da Silva Franchi, Carla Adriene [UNESP]
Boldrin, Natalia Ferreira [UNESP]
Oliveira, Maria Luiza Cotrim Sartor de [UNESP]
Camargo, João Lauro Viana de [UNESP]
dc.subject.por.fl_str_mv diuron (3-[3; 4-dichlorophenyl]-; 1-dimethyl urea)
skin carcinogenesis
initiation-promotion
DMSO
TPA
topic diuron (3-[3; 4-dichlorophenyl]-; 1-dimethyl urea)
skin carcinogenesis
initiation-promotion
DMSO
TPA
description Diuron (3-[3,4-dichlorophenyl]-1,1-dimethyl urea) is an herbicide with carcinogenic activity in rats and mice, which have developed respectively urothelial and mammary gland tumors in long-term studies. Accordingly, diuron has been categorized as a "likely human carcinogen" by the U. S. Environmental Protection Agency. Although the carcinogenesis-initiating activity of diuron has been reported in an early initiation-promotion mouse skin study, its genotoxic potential has been disputed. It is necessary to clarify the mode of action through which it has caused rodent neoplasia and verify its relevance to humans. Herein, two experiments were developed to verify the initiating and promoting potentials of diuron in a twenty-three-and a twenty-one-week-long mouse skin carcinogenesis protocol. In one, dimethylsulfoxide (DMSO) was the solvent for the herbicide; in the other, acetone was the alternative solvent in order to verify whether DMSO had inhibitory influence on a potential cutaneous carcinogenic activity. The adopted schedule for the tumor-promoting agent 12-O-tetradecanoylphorbol 13-acetate (TPA) resulted in skin ulcers, which demonstrates the need for careful selection of TPA dose levels and frequency of application in this model. In both studies, diuron did not exert any influence on the skin carcinogenesis process, in contrast with results already reported in the literature.
publishDate 2010
dc.date.none.fl_str_mv 2010-08-01
2014-05-20T13:37:32Z
2014-05-20T13:37:32Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1177/0192623310375452
Toxicologic Pathology. Thousand Oaks: Sage Publications Inc, v. 38, n. 5, p. 756-764, 2010.
0192-6233
http://hdl.handle.net/11449/13004
10.1177/0192623310375452
WOS:000286314800009
url http://dx.doi.org/10.1177/0192623310375452
http://hdl.handle.net/11449/13004
identifier_str_mv Toxicologic Pathology. Thousand Oaks: Sage Publications Inc, v. 38, n. 5, p. 756-764, 2010.
0192-6233
10.1177/0192623310375452
WOS:000286314800009
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Toxicologic Pathology
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dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 756-764
dc.publisher.none.fl_str_mv Sage Publications Inc
publisher.none.fl_str_mv Sage Publications Inc
dc.source.none.fl_str_mv Web of Science
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv repositoriounesp@unesp.br
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