Cargando…
Organoid Models for Precision Cancer Immunotherapy
Cancer immunotherapy is exploited for the treatment of disease by modulating the immune system. Since the conventional in vivo animal and 2D in vitro models insufficiently recapitulate the complex tumor immune microenvironment (TIME) of the original tumor. In addition, due to the involvement of the...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9016193/ https://www.ncbi.nlm.nih.gov/pubmed/35450073 http://dx.doi.org/10.3389/fimmu.2022.770465 |
_version_ | 1784688476894003200 |
---|---|
author | Sun, Cai-Ping Lan, Huan-Rong Fang, Xing-Liang Yang, Xiao-Yun Jin, Ke-Tao |
author_facet | Sun, Cai-Ping Lan, Huan-Rong Fang, Xing-Liang Yang, Xiao-Yun Jin, Ke-Tao |
author_sort | Sun, Cai-Ping |
collection | PubMed |
description | Cancer immunotherapy is exploited for the treatment of disease by modulating the immune system. Since the conventional in vivo animal and 2D in vitro models insufficiently recapitulate the complex tumor immune microenvironment (TIME) of the original tumor. In addition, due to the involvement of the immune system in cancer immunotherapy, more physiomimetic cancer models, such as patient-derived organoids (PDOs), are required to evaluate the efficacy of immunotherapy agents. On the other hand, the dynamic interactions between the neoplastic cells and non-neoplastic host components in the TIME can promote carcinogenesis, tumor metastasis, cancer progression, and drug resistance of cancer cells. Indeed, tumor organoid models can properly recapitulate the TIME by preserving endogenous stromal components including various immune cells, or by adding exogenous immune cells, cancer-associated fibroblasts (CAFs), vasculature, and other components. Therefore, organoid culture platforms could model immunotherapy responses and facilitate the immunotherapy preclinical testing. Here, we discuss the various organoid culture approaches for the modeling of TIME and the applications of complex tumor organoids in testing cancer immunotherapeutics and personalized cancer immunotherapy. |
format | Online Article Text |
id | pubmed-9016193 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-90161932022-04-20 Organoid Models for Precision Cancer Immunotherapy Sun, Cai-Ping Lan, Huan-Rong Fang, Xing-Liang Yang, Xiao-Yun Jin, Ke-Tao Front Immunol Immunology Cancer immunotherapy is exploited for the treatment of disease by modulating the immune system. Since the conventional in vivo animal and 2D in vitro models insufficiently recapitulate the complex tumor immune microenvironment (TIME) of the original tumor. In addition, due to the involvement of the immune system in cancer immunotherapy, more physiomimetic cancer models, such as patient-derived organoids (PDOs), are required to evaluate the efficacy of immunotherapy agents. On the other hand, the dynamic interactions between the neoplastic cells and non-neoplastic host components in the TIME can promote carcinogenesis, tumor metastasis, cancer progression, and drug resistance of cancer cells. Indeed, tumor organoid models can properly recapitulate the TIME by preserving endogenous stromal components including various immune cells, or by adding exogenous immune cells, cancer-associated fibroblasts (CAFs), vasculature, and other components. Therefore, organoid culture platforms could model immunotherapy responses and facilitate the immunotherapy preclinical testing. Here, we discuss the various organoid culture approaches for the modeling of TIME and the applications of complex tumor organoids in testing cancer immunotherapeutics and personalized cancer immunotherapy. Frontiers Media S.A. 2022-04-05 /pmc/articles/PMC9016193/ /pubmed/35450073 http://dx.doi.org/10.3389/fimmu.2022.770465 Text en Copyright © 2022 Sun, Lan, Fang, Yang and Jin https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Sun, Cai-Ping Lan, Huan-Rong Fang, Xing-Liang Yang, Xiao-Yun Jin, Ke-Tao Organoid Models for Precision Cancer Immunotherapy |
title | Organoid Models for Precision Cancer Immunotherapy |
title_full | Organoid Models for Precision Cancer Immunotherapy |
title_fullStr | Organoid Models for Precision Cancer Immunotherapy |
title_full_unstemmed | Organoid Models for Precision Cancer Immunotherapy |
title_short | Organoid Models for Precision Cancer Immunotherapy |
title_sort | organoid models for precision cancer immunotherapy |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9016193/ https://www.ncbi.nlm.nih.gov/pubmed/35450073 http://dx.doi.org/10.3389/fimmu.2022.770465 |
work_keys_str_mv | AT suncaiping organoidmodelsforprecisioncancerimmunotherapy AT lanhuanrong organoidmodelsforprecisioncancerimmunotherapy AT fangxingliang organoidmodelsforprecisioncancerimmunotherapy AT yangxiaoyun organoidmodelsforprecisioncancerimmunotherapy AT jinketao organoidmodelsforprecisioncancerimmunotherapy |