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Development of humanized mouse with patient‐derived xenografts for cancer immunotherapy studies: A comprehensive review
Immunotherapy has revolutionized cancer treatment, however, not all tumor types and patients are completely responsive to this approach. Establishing predictive pre‐clinical models would allow for more accurate and practical immunotherapeutic drug development. Mouse models are extensively used as in...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8253285/ https://www.ncbi.nlm.nih.gov/pubmed/33938090 http://dx.doi.org/10.1111/cas.14934 |
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author | Jin, Ke‐Tao Du, Wen‐Lin Lan, Huan‐Rong Liu, Yu‐Yao Mao, Chun‐Sen Du, Jin‐Lin Mou, Xiao‐Zhou |
author_facet | Jin, Ke‐Tao Du, Wen‐Lin Lan, Huan‐Rong Liu, Yu‐Yao Mao, Chun‐Sen Du, Jin‐Lin Mou, Xiao‐Zhou |
author_sort | Jin, Ke‐Tao |
collection | PubMed |
description | Immunotherapy has revolutionized cancer treatment, however, not all tumor types and patients are completely responsive to this approach. Establishing predictive pre‐clinical models would allow for more accurate and practical immunotherapeutic drug development. Mouse models are extensively used as in vivo system for biomedical research. However, due to the significant differences between rodents and human, it is impossible to translate most of the findings from mouse models to human. Pharmacological development and advancing personalized medicine using patient‐derived xenografts relies on producing mouse models in which murine cells and genes are substituted with their human equivalent. Humanized mice (HM) provide a suitable platform to evaluate xenograft growth in the context of a human immune system. In this review, we discussed recent advances in the generation and application of HM models. We also reviewed new insights into the basic mechanisms, pre‐clinical evaluation of onco‐immunotherapies, current limitations in the application of these models as well as available improvement strategies. Finally, we pointed out some issues for future studies. |
format | Online Article Text |
id | pubmed-8253285 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-82532852021-07-13 Development of humanized mouse with patient‐derived xenografts for cancer immunotherapy studies: A comprehensive review Jin, Ke‐Tao Du, Wen‐Lin Lan, Huan‐Rong Liu, Yu‐Yao Mao, Chun‐Sen Du, Jin‐Lin Mou, Xiao‐Zhou Cancer Sci Review Articles Immunotherapy has revolutionized cancer treatment, however, not all tumor types and patients are completely responsive to this approach. Establishing predictive pre‐clinical models would allow for more accurate and practical immunotherapeutic drug development. Mouse models are extensively used as in vivo system for biomedical research. However, due to the significant differences between rodents and human, it is impossible to translate most of the findings from mouse models to human. Pharmacological development and advancing personalized medicine using patient‐derived xenografts relies on producing mouse models in which murine cells and genes are substituted with their human equivalent. Humanized mice (HM) provide a suitable platform to evaluate xenograft growth in the context of a human immune system. In this review, we discussed recent advances in the generation and application of HM models. We also reviewed new insights into the basic mechanisms, pre‐clinical evaluation of onco‐immunotherapies, current limitations in the application of these models as well as available improvement strategies. Finally, we pointed out some issues for future studies. John Wiley and Sons Inc. 2021-06-05 2021-07 /pmc/articles/PMC8253285/ /pubmed/33938090 http://dx.doi.org/10.1111/cas.14934 Text en © 2021 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Review Articles Jin, Ke‐Tao Du, Wen‐Lin Lan, Huan‐Rong Liu, Yu‐Yao Mao, Chun‐Sen Du, Jin‐Lin Mou, Xiao‐Zhou Development of humanized mouse with patient‐derived xenografts for cancer immunotherapy studies: A comprehensive review |
title | Development of humanized mouse with patient‐derived xenografts for cancer immunotherapy studies: A comprehensive review |
title_full | Development of humanized mouse with patient‐derived xenografts for cancer immunotherapy studies: A comprehensive review |
title_fullStr | Development of humanized mouse with patient‐derived xenografts for cancer immunotherapy studies: A comprehensive review |
title_full_unstemmed | Development of humanized mouse with patient‐derived xenografts for cancer immunotherapy studies: A comprehensive review |
title_short | Development of humanized mouse with patient‐derived xenografts for cancer immunotherapy studies: A comprehensive review |
title_sort | development of humanized mouse with patient‐derived xenografts for cancer immunotherapy studies: a comprehensive review |
topic | Review Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8253285/ https://www.ncbi.nlm.nih.gov/pubmed/33938090 http://dx.doi.org/10.1111/cas.14934 |
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