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Translation Potential and Challenges of In Vitro and Murine Models in Cancer Clinic

As one of the leading causes of death from disease, cancer continues to pose a serious threat to human health globally. Despite the development of novel therapeutic regimens and drugs, the long-term survival of cancer patients is still very low, especially for those whose diagnosis is not caught ear...

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Autores principales: Long, Yuan, Xie, Bin, Shen, Hong C., Wen, Danyi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9741314/
https://www.ncbi.nlm.nih.gov/pubmed/36497126
http://dx.doi.org/10.3390/cells11233868
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author Long, Yuan
Xie, Bin
Shen, Hong C.
Wen, Danyi
author_facet Long, Yuan
Xie, Bin
Shen, Hong C.
Wen, Danyi
author_sort Long, Yuan
collection PubMed
description As one of the leading causes of death from disease, cancer continues to pose a serious threat to human health globally. Despite the development of novel therapeutic regimens and drugs, the long-term survival of cancer patients is still very low, especially for those whose diagnosis is not caught early enough. Meanwhile, our understanding of tumorigenesis is still limited. Suitable research models are essential tools for exploring cancer mechanisms and treatments. Herein we review and compare several widely used in vitro and in vivo murine cancer models, including syngeneic tumor models, genetically engineered mouse models (GEMM), cell line-derived xenografts (CDX), patient-derived xenografts (PDX), conditionally reprogrammed (CR) cells, organoids, and MiniPDX. We will summarize the methodology and feasibility of various models in terms of their advantages and limitations in the application prospects for drug discovery and development and precision medicine.
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spelling pubmed-97413142022-12-11 Translation Potential and Challenges of In Vitro and Murine Models in Cancer Clinic Long, Yuan Xie, Bin Shen, Hong C. Wen, Danyi Cells Review As one of the leading causes of death from disease, cancer continues to pose a serious threat to human health globally. Despite the development of novel therapeutic regimens and drugs, the long-term survival of cancer patients is still very low, especially for those whose diagnosis is not caught early enough. Meanwhile, our understanding of tumorigenesis is still limited. Suitable research models are essential tools for exploring cancer mechanisms and treatments. Herein we review and compare several widely used in vitro and in vivo murine cancer models, including syngeneic tumor models, genetically engineered mouse models (GEMM), cell line-derived xenografts (CDX), patient-derived xenografts (PDX), conditionally reprogrammed (CR) cells, organoids, and MiniPDX. We will summarize the methodology and feasibility of various models in terms of their advantages and limitations in the application prospects for drug discovery and development and precision medicine. MDPI 2022-11-30 /pmc/articles/PMC9741314/ /pubmed/36497126 http://dx.doi.org/10.3390/cells11233868 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Long, Yuan
Xie, Bin
Shen, Hong C.
Wen, Danyi
Translation Potential and Challenges of In Vitro and Murine Models in Cancer Clinic
title Translation Potential and Challenges of In Vitro and Murine Models in Cancer Clinic
title_full Translation Potential and Challenges of In Vitro and Murine Models in Cancer Clinic
title_fullStr Translation Potential and Challenges of In Vitro and Murine Models in Cancer Clinic
title_full_unstemmed Translation Potential and Challenges of In Vitro and Murine Models in Cancer Clinic
title_short Translation Potential and Challenges of In Vitro and Murine Models in Cancer Clinic
title_sort translation potential and challenges of in vitro and murine models in cancer clinic
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9741314/
https://www.ncbi.nlm.nih.gov/pubmed/36497126
http://dx.doi.org/10.3390/cells11233868
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