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A synthetic metastatic niche reveals antitumor neutrophils drive breast cancer metastatic dormancy in the lungs

Biomaterial scaffolds mimicking the environment in metastatic organs can deconstruct complex signals and facilitate the study of cancer progression and metastasis. Here we report that a subcutaneous scaffold implant in mouse models of metastatic breast cancer in female mice recruits lung-tropic circ...

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Autores principales: Wang, Jing, Ocadiz-Ruiz, Ramon, Hall, Matthew S., Bushnell, Grace G., Orbach, Sophia M., Decker, Joseph T., Raghani, Ravi M., Zhang, Yining, Morris, Aaron H., Jeruss, Jacqueline S., Shea, Lonnie D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10409732/
https://www.ncbi.nlm.nih.gov/pubmed/37553342
http://dx.doi.org/10.1038/s41467-023-40478-5
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author Wang, Jing
Ocadiz-Ruiz, Ramon
Hall, Matthew S.
Bushnell, Grace G.
Orbach, Sophia M.
Decker, Joseph T.
Raghani, Ravi M.
Zhang, Yining
Morris, Aaron H.
Jeruss, Jacqueline S.
Shea, Lonnie D.
author_facet Wang, Jing
Ocadiz-Ruiz, Ramon
Hall, Matthew S.
Bushnell, Grace G.
Orbach, Sophia M.
Decker, Joseph T.
Raghani, Ravi M.
Zhang, Yining
Morris, Aaron H.
Jeruss, Jacqueline S.
Shea, Lonnie D.
author_sort Wang, Jing
collection PubMed
description Biomaterial scaffolds mimicking the environment in metastatic organs can deconstruct complex signals and facilitate the study of cancer progression and metastasis. Here we report that a subcutaneous scaffold implant in mouse models of metastatic breast cancer in female mice recruits lung-tropic circulating tumor cells yet suppresses their growth through potent in situ antitumor immunity. In contrast, the lung, the endogenous metastatic organ for these models, develops lethal metastases in aggressive breast cancer, with less aggressive tumor models developing dormant lungs suppressing tumor growth. Our study reveals multifaceted roles of neutrophils in regulating metastasis. Breast cancer-educated neutrophils infiltrate the scaffold implants and lungs, secreting the same signal to attract lung-tropic circulating tumor cells. Second, antitumor and pro-tumor neutrophils are selectively recruited to the dormant scaffolds and lungs, respectively, responding to distinct groups of chemoattractants to establish activated or suppressive immune environments that direct different fates of cancer cells.
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spelling pubmed-104097322023-08-10 A synthetic metastatic niche reveals antitumor neutrophils drive breast cancer metastatic dormancy in the lungs Wang, Jing Ocadiz-Ruiz, Ramon Hall, Matthew S. Bushnell, Grace G. Orbach, Sophia M. Decker, Joseph T. Raghani, Ravi M. Zhang, Yining Morris, Aaron H. Jeruss, Jacqueline S. Shea, Lonnie D. Nat Commun Article Biomaterial scaffolds mimicking the environment in metastatic organs can deconstruct complex signals and facilitate the study of cancer progression and metastasis. Here we report that a subcutaneous scaffold implant in mouse models of metastatic breast cancer in female mice recruits lung-tropic circulating tumor cells yet suppresses their growth through potent in situ antitumor immunity. In contrast, the lung, the endogenous metastatic organ for these models, develops lethal metastases in aggressive breast cancer, with less aggressive tumor models developing dormant lungs suppressing tumor growth. Our study reveals multifaceted roles of neutrophils in regulating metastasis. Breast cancer-educated neutrophils infiltrate the scaffold implants and lungs, secreting the same signal to attract lung-tropic circulating tumor cells. Second, antitumor and pro-tumor neutrophils are selectively recruited to the dormant scaffolds and lungs, respectively, responding to distinct groups of chemoattractants to establish activated or suppressive immune environments that direct different fates of cancer cells. Nature Publishing Group UK 2023-08-08 /pmc/articles/PMC10409732/ /pubmed/37553342 http://dx.doi.org/10.1038/s41467-023-40478-5 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Wang, Jing
Ocadiz-Ruiz, Ramon
Hall, Matthew S.
Bushnell, Grace G.
Orbach, Sophia M.
Decker, Joseph T.
Raghani, Ravi M.
Zhang, Yining
Morris, Aaron H.
Jeruss, Jacqueline S.
Shea, Lonnie D.
A synthetic metastatic niche reveals antitumor neutrophils drive breast cancer metastatic dormancy in the lungs
title A synthetic metastatic niche reveals antitumor neutrophils drive breast cancer metastatic dormancy in the lungs
title_full A synthetic metastatic niche reveals antitumor neutrophils drive breast cancer metastatic dormancy in the lungs
title_fullStr A synthetic metastatic niche reveals antitumor neutrophils drive breast cancer metastatic dormancy in the lungs
title_full_unstemmed A synthetic metastatic niche reveals antitumor neutrophils drive breast cancer metastatic dormancy in the lungs
title_short A synthetic metastatic niche reveals antitumor neutrophils drive breast cancer metastatic dormancy in the lungs
title_sort synthetic metastatic niche reveals antitumor neutrophils drive breast cancer metastatic dormancy in the lungs
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10409732/
https://www.ncbi.nlm.nih.gov/pubmed/37553342
http://dx.doi.org/10.1038/s41467-023-40478-5
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