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Applications of Genetically Modified Tools to Safety Assessment in Drug Development

The process of new drug development consists of several stages; after identifying potential candidate compounds, preclinical studies using animal models link the laboratory and human clinical trials. Among many steps in preclinical studies, toxicology and safety assessments contribute to identify po...

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Detalles Bibliográficos
Autores principales: Kay, Hee Yeon, Wu, Hongmin, Lee, Seo In, Kim, Sang Geon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Toxicology 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3834461/
https://www.ncbi.nlm.nih.gov/pubmed/24278499
http://dx.doi.org/10.5487/TR.2010.26.1.001
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author Kay, Hee Yeon
Wu, Hongmin
Lee, Seo In
Kim, Sang Geon
author_facet Kay, Hee Yeon
Wu, Hongmin
Lee, Seo In
Kim, Sang Geon
author_sort Kay, Hee Yeon
collection PubMed
description The process of new drug development consists of several stages; after identifying potential candidate compounds, preclinical studies using animal models link the laboratory and human clinical trials. Among many steps in preclinical studies, toxicology and safety assessments contribute to identify potential adverse events and provide rationale for setting the initial doses in clinical trials. Gene modulation is one of the important tools of modern biology, and is commonly employed to examine the function of genes of interest. Advances in new drug development have been achieved by exploding information on target selection and validation using genetically modified animal models as well as those of cells. In this review, a recent trend of genetically modified methods is discussed with reference to safety assessments, and the exemplary applications of gene-modulating tools to the tests in new drug development were summarized.
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spelling pubmed-38344612013-11-25 Applications of Genetically Modified Tools to Safety Assessment in Drug Development Kay, Hee Yeon Wu, Hongmin Lee, Seo In Kim, Sang Geon Toxicol Res Article The process of new drug development consists of several stages; after identifying potential candidate compounds, preclinical studies using animal models link the laboratory and human clinical trials. Among many steps in preclinical studies, toxicology and safety assessments contribute to identify potential adverse events and provide rationale for setting the initial doses in clinical trials. Gene modulation is one of the important tools of modern biology, and is commonly employed to examine the function of genes of interest. Advances in new drug development have been achieved by exploding information on target selection and validation using genetically modified animal models as well as those of cells. In this review, a recent trend of genetically modified methods is discussed with reference to safety assessments, and the exemplary applications of gene-modulating tools to the tests in new drug development were summarized. The Korean Society of Toxicology 2010-03 /pmc/articles/PMC3834461/ /pubmed/24278499 http://dx.doi.org/10.5487/TR.2010.26.1.001 Text en Copyright ©2010, The Korean Society of Toxicology
spellingShingle Article
Kay, Hee Yeon
Wu, Hongmin
Lee, Seo In
Kim, Sang Geon
Applications of Genetically Modified Tools to Safety Assessment in Drug Development
title Applications of Genetically Modified Tools to Safety Assessment in Drug Development
title_full Applications of Genetically Modified Tools to Safety Assessment in Drug Development
title_fullStr Applications of Genetically Modified Tools to Safety Assessment in Drug Development
title_full_unstemmed Applications of Genetically Modified Tools to Safety Assessment in Drug Development
title_short Applications of Genetically Modified Tools to Safety Assessment in Drug Development
title_sort applications of genetically modified tools to safety assessment in drug development
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3834461/
https://www.ncbi.nlm.nih.gov/pubmed/24278499
http://dx.doi.org/10.5487/TR.2010.26.1.001
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