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Patient-derived xenograft mouse models: A high fidelity tool for individualized medicine

Patient-derived xenograft (PDX) mouse models involve the direct transfer of fresh human tumor samples into immunodeficient mice following surgical resection or other medical operations. Gene expression in tumors may be maintained by serial passages of tumors from mouse to mouse. These models aid res...

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Detalles Bibliográficos
Autores principales: Xu, Cong, Li, Xuelu, Liu, Pixu, Li, Man, Luo, Fuwen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6313209/
https://www.ncbi.nlm.nih.gov/pubmed/30655732
http://dx.doi.org/10.3892/ol.2018.9583
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author Xu, Cong
Li, Xuelu
Liu, Pixu
Li, Man
Luo, Fuwen
author_facet Xu, Cong
Li, Xuelu
Liu, Pixu
Li, Man
Luo, Fuwen
author_sort Xu, Cong
collection PubMed
description Patient-derived xenograft (PDX) mouse models involve the direct transfer of fresh human tumor samples into immunodeficient mice following surgical resection or other medical operations. Gene expression in tumors may be maintained by serial passages of tumors from mouse to mouse. These models aid research into tumor biology and pharmacology without manual manipulation of cell cultures in vitro. and are widely used in individualized cancer therapy/translational medicine, drug development and coclinical trials. PDX models exhibit higher predictive values for clinical outcomes than cell line-derived xenograft models and genetically engineered mouse models. However, PDX models are associated with certain challenges in clinical application. The present study reviewed current collections of PDX models and assessed the challenges and future directions of this field.
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spelling pubmed-63132092019-01-17 Patient-derived xenograft mouse models: A high fidelity tool for individualized medicine Xu, Cong Li, Xuelu Liu, Pixu Li, Man Luo, Fuwen Oncol Lett Review Patient-derived xenograft (PDX) mouse models involve the direct transfer of fresh human tumor samples into immunodeficient mice following surgical resection or other medical operations. Gene expression in tumors may be maintained by serial passages of tumors from mouse to mouse. These models aid research into tumor biology and pharmacology without manual manipulation of cell cultures in vitro. and are widely used in individualized cancer therapy/translational medicine, drug development and coclinical trials. PDX models exhibit higher predictive values for clinical outcomes than cell line-derived xenograft models and genetically engineered mouse models. However, PDX models are associated with certain challenges in clinical application. The present study reviewed current collections of PDX models and assessed the challenges and future directions of this field. D.A. Spandidos 2019-01 2018-10-16 /pmc/articles/PMC6313209/ /pubmed/30655732 http://dx.doi.org/10.3892/ol.2018.9583 Text en Copyright: © Xu et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Review
Xu, Cong
Li, Xuelu
Liu, Pixu
Li, Man
Luo, Fuwen
Patient-derived xenograft mouse models: A high fidelity tool for individualized medicine
title Patient-derived xenograft mouse models: A high fidelity tool for individualized medicine
title_full Patient-derived xenograft mouse models: A high fidelity tool for individualized medicine
title_fullStr Patient-derived xenograft mouse models: A high fidelity tool for individualized medicine
title_full_unstemmed Patient-derived xenograft mouse models: A high fidelity tool for individualized medicine
title_short Patient-derived xenograft mouse models: A high fidelity tool for individualized medicine
title_sort patient-derived xenograft mouse models: a high fidelity tool for individualized medicine
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6313209/
https://www.ncbi.nlm.nih.gov/pubmed/30655732
http://dx.doi.org/10.3892/ol.2018.9583
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