Tissues and Tumor Microenvironment (TME) in 3D: Models to Shed Light on Immunosuppression in Cancer

Immunosuppression in cancer has emerged as a major hurdle to immunotherapy efforts. Immunosuppression can arise from oncogene-induced signaling within the tumor as well as from tumor-associated immune cells. Understanding various mechanisms by which the tumor can undermine and evade therapy is criti...

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Main Authors: Teresa Ho, Rasha Msallam
Format: Article
Language:English
Published: MDPI AG 2021-04-01
Series:Cells
Subjects:
Online Access:https://www.mdpi.com/2073-4409/10/4/831
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spelling doaj-1b193ff66b674699ac29eca15955ec582021-04-07T23:02:28ZengMDPI AGCells2073-44092021-04-011083183110.3390/cells10040831Tissues and Tumor Microenvironment (TME) in 3D: Models to Shed Light on Immunosuppression in CancerTeresa Ho0Rasha Msallam1p53Lab, Agency for Science, Technology and Research (A*STAR), 8A Biomedical Grove, Neu-ros/Immunos, #06-04/05, Singapore 138648, SingaporeLaboratory for Translational and Molecular Imaging (LTMI), Cancer and Stem Cell Biology Pro-gramme, Duke-NUS Medical School, 8 College Road, Singapore 169857, SingaporeImmunosuppression in cancer has emerged as a major hurdle to immunotherapy efforts. Immunosuppression can arise from oncogene-induced signaling within the tumor as well as from tumor-associated immune cells. Understanding various mechanisms by which the tumor can undermine and evade therapy is critical in improving current cancer immunotherapies. While mouse models have allowed for the characterization of key immune cell types and their role in tumor development, extrapolating these mechanisms to patients has been challenging. There is need for better models to unravel the effects of genetic alterations inherent in tumor cells and immune cells isolated from tumors on tumor growth and to investigate the feasibility of immunotherapy. Three-dimensional (3D) organoid model systems have developed rapidly over the past few years and allow for incorporation of components of the tumor microenvironment such as immune cells and the stroma. This bears great promise for derivation of patient-specific models in a dish for understanding and determining the impact on personalized immunotherapy. In this review, we will highlight the significance of current experimental models employed in the study of tumor immunosuppression and evaluate current tumor organoid-immune cell co-culture systems and their potential impact in shedding light on cancer immunosuppression.https://www.mdpi.com/2073-4409/10/4/831organoidimmunosuppressiontumor microenvironmentMDSChumanized mouse models
collection DOAJ
language English
format Article
sources DOAJ
author Teresa Ho
Rasha Msallam
spellingShingle Teresa Ho
Rasha Msallam
Tissues and Tumor Microenvironment (TME) in 3D: Models to Shed Light on Immunosuppression in Cancer
Cells
organoid
immunosuppression
tumor microenvironment
MDSC
humanized mouse models
author_facet Teresa Ho
Rasha Msallam
author_sort Teresa Ho
title Tissues and Tumor Microenvironment (TME) in 3D: Models to Shed Light on Immunosuppression in Cancer
title_short Tissues and Tumor Microenvironment (TME) in 3D: Models to Shed Light on Immunosuppression in Cancer
title_full Tissues and Tumor Microenvironment (TME) in 3D: Models to Shed Light on Immunosuppression in Cancer
title_fullStr Tissues and Tumor Microenvironment (TME) in 3D: Models to Shed Light on Immunosuppression in Cancer
title_full_unstemmed Tissues and Tumor Microenvironment (TME) in 3D: Models to Shed Light on Immunosuppression in Cancer
title_sort tissues and tumor microenvironment (tme) in 3d: models to shed light on immunosuppression in cancer
publisher MDPI AG
series Cells
issn 2073-4409
publishDate 2021-04-01
description Immunosuppression in cancer has emerged as a major hurdle to immunotherapy efforts. Immunosuppression can arise from oncogene-induced signaling within the tumor as well as from tumor-associated immune cells. Understanding various mechanisms by which the tumor can undermine and evade therapy is critical in improving current cancer immunotherapies. While mouse models have allowed for the characterization of key immune cell types and their role in tumor development, extrapolating these mechanisms to patients has been challenging. There is need for better models to unravel the effects of genetic alterations inherent in tumor cells and immune cells isolated from tumors on tumor growth and to investigate the feasibility of immunotherapy. Three-dimensional (3D) organoid model systems have developed rapidly over the past few years and allow for incorporation of components of the tumor microenvironment such as immune cells and the stroma. This bears great promise for derivation of patient-specific models in a dish for understanding and determining the impact on personalized immunotherapy. In this review, we will highlight the significance of current experimental models employed in the study of tumor immunosuppression and evaluate current tumor organoid-immune cell co-culture systems and their potential impact in shedding light on cancer immunosuppression.
topic organoid
immunosuppression
tumor microenvironment
MDSC
humanized mouse models
url https://www.mdpi.com/2073-4409/10/4/831
work_keys_str_mv AT teresaho tissuesandtumormicroenvironmenttmein3dmodelstoshedlightonimmunosuppressionincancer
AT rashamsallam tissuesandtumormicroenvironmenttmein3dmodelstoshedlightonimmunosuppressionincancer
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