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A Tumor-admixture Model to Interrogate Immune Cell–dependent Tumorigenesis

A rigorous determination of effector contributions of tumor-infiltrating immune cells is critical for identifying targetable molecular mechanisms for the development of novel cancer immunotherapies. A tumor/immune cell–admixture model is an advantageous strategy to study tumor immunology as the fund...

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Autores principales: Noe, Jordan T., Ding, Chuanlin, Geller, Anne E., Rendon, Beatriz E., Yan, Jun, Mitchell, Robert A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bio-Protocol 202
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9993080/
https://www.ncbi.nlm.nih.gov/pubmed/36908637
http://dx.doi.org/ 10.21769/BioProtoc.4630
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author Noe, Jordan T.
Ding, Chuanlin
Geller, Anne E.
Rendon, Beatriz E.
Yan, Jun
Mitchell, Robert A.
author_facet Noe, Jordan T.
Ding, Chuanlin
Geller, Anne E.
Rendon, Beatriz E.
Yan, Jun
Mitchell, Robert A.
author_sort Noe, Jordan T.
collection PubMed
description A rigorous determination of effector contributions of tumor-infiltrating immune cells is critical for identifying targetable molecular mechanisms for the development of novel cancer immunotherapies. A tumor/immune cell–admixture model is an advantageous strategy to study tumor immunology as the fundamental methodology is relatively straightforward, while also being adaptable to scale to address increasingly complex research queries. Ultimately, this method can provide robust experimental information to complement more traditional murine models of tumor immunology. Here, we describe a tumor/macrophage-admixture model using bone marrow–derived macrophages to investigate macrophage-dependent tumorigenesis. Additionally, we provide commentary on potential branch points for optimization with other immune cells, experimental techniques, and cancer types.
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spelling pubmed-99930802023-03-09 A Tumor-admixture Model to Interrogate Immune Cell–dependent Tumorigenesis Noe, Jordan T. Ding, Chuanlin Geller, Anne E. Rendon, Beatriz E. Yan, Jun Mitchell, Robert A. Bio Protoc Methods Article A rigorous determination of effector contributions of tumor-infiltrating immune cells is critical for identifying targetable molecular mechanisms for the development of novel cancer immunotherapies. A tumor/immune cell–admixture model is an advantageous strategy to study tumor immunology as the fundamental methodology is relatively straightforward, while also being adaptable to scale to address increasingly complex research queries. Ultimately, this method can provide robust experimental information to complement more traditional murine models of tumor immunology. Here, we describe a tumor/macrophage-admixture model using bone marrow–derived macrophages to investigate macrophage-dependent tumorigenesis. Additionally, we provide commentary on potential branch points for optimization with other immune cells, experimental techniques, and cancer types. Bio-Protocol 2023 -03- 05 /pmc/articles/PMC9993080/ /pubmed/36908637 http://dx.doi.org/ 10.21769/BioProtoc.4630 Text en Copyright © 2023 The Authors; exclusive licensee Bio-protocol LLC. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the CC BY-NC license (https://creativecommons.org/licenses/by-nc/4.0/).
spellingShingle Methods Article
Noe, Jordan T.
Ding, Chuanlin
Geller, Anne E.
Rendon, Beatriz E.
Yan, Jun
Mitchell, Robert A.
A Tumor-admixture Model to Interrogate Immune Cell–dependent Tumorigenesis
title A Tumor-admixture Model to Interrogate Immune Cell–dependent Tumorigenesis
title_full A Tumor-admixture Model to Interrogate Immune Cell–dependent Tumorigenesis
title_fullStr A Tumor-admixture Model to Interrogate Immune Cell–dependent Tumorigenesis
title_full_unstemmed A Tumor-admixture Model to Interrogate Immune Cell–dependent Tumorigenesis
title_short A Tumor-admixture Model to Interrogate Immune Cell–dependent Tumorigenesis
title_sort tumor-admixture model to interrogate immune cell–dependent tumorigenesis
topic Methods Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9993080/
https://www.ncbi.nlm.nih.gov/pubmed/36908637
http://dx.doi.org/ 10.21769/BioProtoc.4630
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