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Cell transformation assays for prediction of carcinogenic potential: state of the science and future research needs

Cell transformation assays (CTAs) have long been proposed as in vitro methods for the identification of potential chemical carcinogens. Despite showing good correlation with rodent bioassay data, concerns over the subjective nature of using morphological criteria for identifying transformed cells an...

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Autores principales: Creton, Stuart, Aardema, Marilyn J., Carmichael, Paul L., Harvey, James S., Martin, Francis L., Newbold, Robert F., O’Donovan, Michael R., Pant, Kamala, Poth, Albrecht, Sakai, Ayako, Sasaki, Kiyoshi, Scott, Andrew D., Schechtman, Leonard M., Shen, Rhine R., Tanaka, Noriho, Yasaei, Hemad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3241940/
https://www.ncbi.nlm.nih.gov/pubmed/21852270
http://dx.doi.org/10.1093/mutage/ger053
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author Creton, Stuart
Aardema, Marilyn J.
Carmichael, Paul L.
Harvey, James S.
Martin, Francis L.
Newbold, Robert F.
O’Donovan, Michael R.
Pant, Kamala
Poth, Albrecht
Sakai, Ayako
Sasaki, Kiyoshi
Scott, Andrew D.
Schechtman, Leonard M.
Shen, Rhine R.
Tanaka, Noriho
Yasaei, Hemad
author_facet Creton, Stuart
Aardema, Marilyn J.
Carmichael, Paul L.
Harvey, James S.
Martin, Francis L.
Newbold, Robert F.
O’Donovan, Michael R.
Pant, Kamala
Poth, Albrecht
Sakai, Ayako
Sasaki, Kiyoshi
Scott, Andrew D.
Schechtman, Leonard M.
Shen, Rhine R.
Tanaka, Noriho
Yasaei, Hemad
author_sort Creton, Stuart
collection PubMed
description Cell transformation assays (CTAs) have long been proposed as in vitro methods for the identification of potential chemical carcinogens. Despite showing good correlation with rodent bioassay data, concerns over the subjective nature of using morphological criteria for identifying transformed cells and a lack of understanding of the mechanistic basis of the assays has limited their acceptance for regulatory purposes. However, recent drivers to find alternative carcinogenicity assessment methodologies, such as the Seventh Amendment to the EU Cosmetics Directive, have fuelled renewed interest in CTAs. Research is currently ongoing to improve the objectivity of the assays, reveal the underlying molecular changes leading to transformation and explore the use of novel cell types. The UK NC3Rs held an international workshop in November 2010 to review the current state of the art in this field and provide directions for future research. This paper outlines the key points highlighted at this meeting.
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spelling pubmed-32419402011-12-19 Cell transformation assays for prediction of carcinogenic potential: state of the science and future research needs Creton, Stuart Aardema, Marilyn J. Carmichael, Paul L. Harvey, James S. Martin, Francis L. Newbold, Robert F. O’Donovan, Michael R. Pant, Kamala Poth, Albrecht Sakai, Ayako Sasaki, Kiyoshi Scott, Andrew D. Schechtman, Leonard M. Shen, Rhine R. Tanaka, Noriho Yasaei, Hemad Mutagenesis Meeting Report Cell transformation assays (CTAs) have long been proposed as in vitro methods for the identification of potential chemical carcinogens. Despite showing good correlation with rodent bioassay data, concerns over the subjective nature of using morphological criteria for identifying transformed cells and a lack of understanding of the mechanistic basis of the assays has limited their acceptance for regulatory purposes. However, recent drivers to find alternative carcinogenicity assessment methodologies, such as the Seventh Amendment to the EU Cosmetics Directive, have fuelled renewed interest in CTAs. Research is currently ongoing to improve the objectivity of the assays, reveal the underlying molecular changes leading to transformation and explore the use of novel cell types. The UK NC3Rs held an international workshop in November 2010 to review the current state of the art in this field and provide directions for future research. This paper outlines the key points highlighted at this meeting. Oxford University Press 2012-01 2011-08-17 /pmc/articles/PMC3241940/ /pubmed/21852270 http://dx.doi.org/10.1093/mutage/ger053 Text en © 2011 The Authors. Published by Oxford University Press on behalf of the UK Environmental Mutagen Society. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Meeting Report
Creton, Stuart
Aardema, Marilyn J.
Carmichael, Paul L.
Harvey, James S.
Martin, Francis L.
Newbold, Robert F.
O’Donovan, Michael R.
Pant, Kamala
Poth, Albrecht
Sakai, Ayako
Sasaki, Kiyoshi
Scott, Andrew D.
Schechtman, Leonard M.
Shen, Rhine R.
Tanaka, Noriho
Yasaei, Hemad
Cell transformation assays for prediction of carcinogenic potential: state of the science and future research needs
title Cell transformation assays for prediction of carcinogenic potential: state of the science and future research needs
title_full Cell transformation assays for prediction of carcinogenic potential: state of the science and future research needs
title_fullStr Cell transformation assays for prediction of carcinogenic potential: state of the science and future research needs
title_full_unstemmed Cell transformation assays for prediction of carcinogenic potential: state of the science and future research needs
title_short Cell transformation assays for prediction of carcinogenic potential: state of the science and future research needs
title_sort cell transformation assays for prediction of carcinogenic potential: state of the science and future research needs
topic Meeting Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3241940/
https://www.ncbi.nlm.nih.gov/pubmed/21852270
http://dx.doi.org/10.1093/mutage/ger053
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