Cargando…

Nonlinearity of dose-response functions for carcinogenicity.

Carcinogenesis data for 315 chemicals were obtained from the National Cancer Institute-National Toxicology Program (NCI-NTP) bioassay programs and were analyzed to examine the shape of carcinogenesis dose-response curves. Tumor site data were more often consistent with a quadratic response than with...

Descripción completa

Detalles Bibliográficos
Autores principales: Hoel, D G, Portier, C J
Formato: Texto
Lenguaje:English
Publicado: 1994
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1566901/
https://www.ncbi.nlm.nih.gov/pubmed/8187698
_version_ 1782129716183957504
author Hoel, D G
Portier, C J
author_facet Hoel, D G
Portier, C J
author_sort Hoel, D G
collection PubMed
description Carcinogenesis data for 315 chemicals were obtained from the National Cancer Institute-National Toxicology Program (NCI-NTP) bioassay programs and were analyzed to examine the shape of carcinogenesis dose-response curves. Tumor site data were more often consistent with a quadratic response than with a linear response, suggesting that the routine use of linear dose-response models will often overestimate risk. Information from in vivo short-term mutagenicity and genotoxicity assays was also obtained for most of these rodent bioassays. It was found that there were no clear relationships between the shape of the carcinogenesis dose-response curve and the result of the short-term test. These observations argue against the concept that carcinogens that are positive in a short-term assay be regulated using a linear dose-response curve and those that are negative be regulated using a sublinear dose-response curve or a safety factor approach.
format Text
id pubmed-1566901
institution National Center for Biotechnology Information
language English
publishDate 1994
record_format MEDLINE/PubMed
spelling pubmed-15669012006-09-19 Nonlinearity of dose-response functions for carcinogenicity. Hoel, D G Portier, C J Environ Health Perspect Research Article Carcinogenesis data for 315 chemicals were obtained from the National Cancer Institute-National Toxicology Program (NCI-NTP) bioassay programs and were analyzed to examine the shape of carcinogenesis dose-response curves. Tumor site data were more often consistent with a quadratic response than with a linear response, suggesting that the routine use of linear dose-response models will often overestimate risk. Information from in vivo short-term mutagenicity and genotoxicity assays was also obtained for most of these rodent bioassays. It was found that there were no clear relationships between the shape of the carcinogenesis dose-response curve and the result of the short-term test. These observations argue against the concept that carcinogens that are positive in a short-term assay be regulated using a linear dose-response curve and those that are negative be regulated using a sublinear dose-response curve or a safety factor approach. 1994-01 /pmc/articles/PMC1566901/ /pubmed/8187698 Text en
spellingShingle Research Article
Hoel, D G
Portier, C J
Nonlinearity of dose-response functions for carcinogenicity.
title Nonlinearity of dose-response functions for carcinogenicity.
title_full Nonlinearity of dose-response functions for carcinogenicity.
title_fullStr Nonlinearity of dose-response functions for carcinogenicity.
title_full_unstemmed Nonlinearity of dose-response functions for carcinogenicity.
title_short Nonlinearity of dose-response functions for carcinogenicity.
title_sort nonlinearity of dose-response functions for carcinogenicity.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1566901/
https://www.ncbi.nlm.nih.gov/pubmed/8187698
work_keys_str_mv AT hoeldg nonlinearityofdoseresponsefunctionsforcarcinogenicity
AT portiercj nonlinearityofdoseresponsefunctionsforcarcinogenicity