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Human Tumor Xenograft Models for Preclinical Assessment of Anticancer Drug Development

Xenograft models of human cancer play an important role in the screening and evaluation of candidates for new anticancer agents. The models, which are derived from human tumor cell lines and are classified according to the transplant site, such as ectopic xenograft and orthotopic xenograft, are stil...

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Autor principal: Jung, Joohee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society Of Toxicology 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4007037/
https://www.ncbi.nlm.nih.gov/pubmed/24795792
http://dx.doi.org/10.5487/TR.2014.30.1.001
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author Jung, Joohee
author_facet Jung, Joohee
author_sort Jung, Joohee
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description Xenograft models of human cancer play an important role in the screening and evaluation of candidates for new anticancer agents. The models, which are derived from human tumor cell lines and are classified according to the transplant site, such as ectopic xenograft and orthotopic xenograft, are still utilized to evaluate therapeutic efficacy and toxicity. The metastasis model is modified for the evaluation and prediction of cancer progression. Recently, animal models are made from patient-derived tumor tissue. The patient-derived tumor xenograft models with physiological characters similar to those of patients have been established for personalized medicine. In the discovery of anticancer drugs, standard animal models save time and money and provide evidence to support clinical trials. The current strategy for using xenograft models as an informative tool is introduced.
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spelling pubmed-40070372014-05-02 Human Tumor Xenograft Models for Preclinical Assessment of Anticancer Drug Development Jung, Joohee Toxicol Res Articles Xenograft models of human cancer play an important role in the screening and evaluation of candidates for new anticancer agents. The models, which are derived from human tumor cell lines and are classified according to the transplant site, such as ectopic xenograft and orthotopic xenograft, are still utilized to evaluate therapeutic efficacy and toxicity. The metastasis model is modified for the evaluation and prediction of cancer progression. Recently, animal models are made from patient-derived tumor tissue. The patient-derived tumor xenograft models with physiological characters similar to those of patients have been established for personalized medicine. In the discovery of anticancer drugs, standard animal models save time and money and provide evidence to support clinical trials. The current strategy for using xenograft models as an informative tool is introduced. The Korean Society Of Toxicology 2014-03 /pmc/articles/PMC4007037/ /pubmed/24795792 http://dx.doi.org/10.5487/TR.2014.30.1.001 Text en Copyright © 2014, The Korean Society Of Toxicology 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 Articles
Jung, Joohee
Human Tumor Xenograft Models for Preclinical Assessment of Anticancer Drug Development
title Human Tumor Xenograft Models for Preclinical Assessment of Anticancer Drug Development
title_full Human Tumor Xenograft Models for Preclinical Assessment of Anticancer Drug Development
title_fullStr Human Tumor Xenograft Models for Preclinical Assessment of Anticancer Drug Development
title_full_unstemmed Human Tumor Xenograft Models for Preclinical Assessment of Anticancer Drug Development
title_short Human Tumor Xenograft Models for Preclinical Assessment of Anticancer Drug Development
title_sort human tumor xenograft models for preclinical assessment of anticancer drug development
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4007037/
https://www.ncbi.nlm.nih.gov/pubmed/24795792
http://dx.doi.org/10.5487/TR.2014.30.1.001
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