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Locally sourced: site-specific immune barriers to metastasis

Tumour cells migrate very early from primary sites to distant sites, and yet metastases often take years to manifest themselves clinically or never even surface within a patient’s lifetime. This pause in cancer progression emphasizes the existence of barriers that constrain the growth of disseminate...

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Autor principal: Correia, Ana Luísa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9904275/
https://www.ncbi.nlm.nih.gov/pubmed/36750616
http://dx.doi.org/10.1038/s41577-023-00836-2
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author Correia, Ana Luísa
author_facet Correia, Ana Luísa
author_sort Correia, Ana Luísa
collection PubMed
description Tumour cells migrate very early from primary sites to distant sites, and yet metastases often take years to manifest themselves clinically or never even surface within a patient’s lifetime. This pause in cancer progression emphasizes the existence of barriers that constrain the growth of disseminated tumour cells (DTCs) at distant sites. Although the nature of these barriers to metastasis might include DTC-intrinsic traits, recent studies have established that the local microenvironment also controls the formation of metastases. In this Perspective, I discuss how site-specific differences of the immune system might be a major selective growth restraint on DTCs, and argue that harnessing tissue immunity will be essential for the next stage in immunotherapy development that reliably prevents the establishment of metastases.
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spelling pubmed-99042752023-02-07 Locally sourced: site-specific immune barriers to metastasis Correia, Ana Luísa Nat Rev Immunol Perspective Tumour cells migrate very early from primary sites to distant sites, and yet metastases often take years to manifest themselves clinically or never even surface within a patient’s lifetime. This pause in cancer progression emphasizes the existence of barriers that constrain the growth of disseminated tumour cells (DTCs) at distant sites. Although the nature of these barriers to metastasis might include DTC-intrinsic traits, recent studies have established that the local microenvironment also controls the formation of metastases. In this Perspective, I discuss how site-specific differences of the immune system might be a major selective growth restraint on DTCs, and argue that harnessing tissue immunity will be essential for the next stage in immunotherapy development that reliably prevents the establishment of metastases. Nature Publishing Group UK 2023-02-07 /pmc/articles/PMC9904275/ /pubmed/36750616 http://dx.doi.org/10.1038/s41577-023-00836-2 Text en © Springer Nature Limited 2023, Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Perspective
Correia, Ana Luísa
Locally sourced: site-specific immune barriers to metastasis
title Locally sourced: site-specific immune barriers to metastasis
title_full Locally sourced: site-specific immune barriers to metastasis
title_fullStr Locally sourced: site-specific immune barriers to metastasis
title_full_unstemmed Locally sourced: site-specific immune barriers to metastasis
title_short Locally sourced: site-specific immune barriers to metastasis
title_sort locally sourced: site-specific immune barriers to metastasis
topic Perspective
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9904275/
https://www.ncbi.nlm.nih.gov/pubmed/36750616
http://dx.doi.org/10.1038/s41577-023-00836-2
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