The utility of genetically modified mouse assays for identifying human carcinogens: a basic understanding and path forward. The Alternatives to Carcinogenicity Testing Committee ILSI HESI
- PMID: 14657512
- DOI: 10.1093/toxsci/kfh037
The utility of genetically modified mouse assays for identifying human carcinogens: a basic understanding and path forward. The Alternatives to Carcinogenicity Testing Committee ILSI HESI
Abstract
The Alternatives to Carcinogenicity Testing Committee of the International Life Sciences Institute (ILSI) Health and Environmental Sciences Institute (HESI) conducted a large-scale, multinational collaborative research program to evaluate several genetically modified mouse assays for assessing the human carcinogenic potential of compounds. The data from this testing program have made an important contribution to the general understanding of how these models can be best applied in hazard identification; however, questions still exist regarding methodology and data interpretation. To address these issues, ILSI HESI hosted a February 2003 workshop on the Utility of Transgenic Assays for Risk Assessment. The purpose of this workshop was to reach an understanding of how data from genetically modified mouse models are viewed by different regulatory bodies in the pharmaceutical sector and, based on this understanding, to identify areas in which more experimental work may be needed to increase the utility of data derived from these assays. In the course of discussions, various data gaps related to model selection and protocol issues were identified. Based on the outcome of the workshop, various studies are proposed to provide data to improve the utility of currently available assays for cancer hazard identification and risk assessment purposes.
Similar articles
-
The in vivo rodent test systems for assessment of carcinogenic potential.Regul Toxicol Pharmacol. 2002 Feb;35(1):122-5. doi: 10.1006/rtph.2001.1505. Regul Toxicol Pharmacol. 2002. PMID: 11846641
-
Background and framework for ILSI's collaborative evaluation program on alternative models for carcinogenicity assessment. International Life Sciences Institute.Toxicol Pathol. 2001;29 Suppl:13-9. doi: 10.1080/019262301753178438. Toxicol Pathol. 2001. PMID: 11695549 Review.
-
The transgenic mouse assay as an alternative test method for regulatory carcinogenicity studies--implications for REACH.Regul Toxicol Pharmacol. 2009 Mar;53(2):150-5. doi: 10.1016/j.yrtph.2008.12.006. Epub 2008 Dec 25. Regul Toxicol Pharmacol. 2009. PMID: 19126422
-
Use of genetically modified mouse models for evaluation of carcinogenic risk: considerations for the laboratory animal scientist.Comp Med. 2001 Oct;51(5):399-405. Comp Med. 2001. PMID: 11924798 Review.
-
Issues in the design and interpretation of chronic toxicity and carcinogenicity studies in rodents: approaches to dose selection.Crit Rev Toxicol. 2007;37(9):729-837. doi: 10.1080/10408440701524949. Crit Rev Toxicol. 2007. PMID: 17957539 Review.
Cited by
-
Oncogenicity evaluation of resveratrol in p53(+/-) (p53 knockout) mice.Food Chem Toxicol. 2007 Jan;45(1):55-63. doi: 10.1016/j.fct.2006.07.015. Epub 2006 Aug 8. Food Chem Toxicol. 2007. PMID: 16965847 Free PMC article.
-
Progression process and safety assessment adaptation of endometrial lesions in ENU-induced 2-stage uterine carcinogenicity in a Tg-rasH2 mouse model.J Toxicol Pathol. 2018 Jan;31(1):35-41. doi: 10.1293/tox.2017-0035. Epub 2017 Sep 21. J Toxicol Pathol. 2018. PMID: 29479138 Free PMC article.
-
Creation and preliminary characterization of a Tp53 knockout rat.Dis Model Mech. 2013 Jan;6(1):269-78. doi: 10.1242/dmm.009704. Epub 2012 Aug 23. Dis Model Mech. 2013. PMID: 22917926 Free PMC article.
-
3S - Systematic, systemic, and systems biology and toxicology.ALTEX. 2018;35(2):139-162. doi: 10.14573/altex.1804051. ALTEX. 2018. PMID: 29677694 Free PMC article.
-
Detection of the onset of ischemia and carcinogenesis by hypoxia-inducible transcription factor-based in vivo bioluminescence imaging.PLoS One. 2011;6(11):e26640. doi: 10.1371/journal.pone.0026640. Epub 2011 Nov 10. PLoS One. 2011. PMID: 22102864 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources