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Cancer Stemness Meets Immunity: From Mechanism to Therapy
Cancer stem cells (CSCs) are self-renewing cells that facilitate tumor initiation, promote metastasis, and enhance cancer therapy resistance. Transcriptomic analyses across many cancer types have revealed a prominent association between stemness and immune signatures, potentially implying a biologic...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7839836/ https://www.ncbi.nlm.nih.gov/pubmed/33406434 http://dx.doi.org/10.1016/j.celrep.2020.108597 |
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author | Chen, Peiwen Hsu, Wen-Hao Han, Jincheng Xia, Yan DePinho, Ronald A. |
author_facet | Chen, Peiwen Hsu, Wen-Hao Han, Jincheng Xia, Yan DePinho, Ronald A. |
author_sort | Chen, Peiwen |
collection | PubMed |
description | Cancer stem cells (CSCs) are self-renewing cells that facilitate tumor initiation, promote metastasis, and enhance cancer therapy resistance. Transcriptomic analyses across many cancer types have revealed a prominent association between stemness and immune signatures, potentially implying a biological interaction between such hallmark features of cancer. Emerging experimental evidence has substantiated the influence of CSCs on immune cells, including tumor-associated macrophages, myeloid-derived suppressor cells, and T cells, in the tumor microenvironment and, reciprocally, the importance of such immune cells in sustaining CSC stemness and its survival niche. This review covers the cellular and molecular mechanisms underlying the symbiotic interactions between CSCs and immune cells and how such heterotypic signaling maintains a tumor-promoting ecosystem and informs therapeutic strategies intercepting this co-dependency. |
format | Online Article Text |
id | pubmed-7839836 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
record_format | MEDLINE/PubMed |
spelling | pubmed-78398362021-01-27 Cancer Stemness Meets Immunity: From Mechanism to Therapy Chen, Peiwen Hsu, Wen-Hao Han, Jincheng Xia, Yan DePinho, Ronald A. Cell Rep Article Cancer stem cells (CSCs) are self-renewing cells that facilitate tumor initiation, promote metastasis, and enhance cancer therapy resistance. Transcriptomic analyses across many cancer types have revealed a prominent association between stemness and immune signatures, potentially implying a biological interaction between such hallmark features of cancer. Emerging experimental evidence has substantiated the influence of CSCs on immune cells, including tumor-associated macrophages, myeloid-derived suppressor cells, and T cells, in the tumor microenvironment and, reciprocally, the importance of such immune cells in sustaining CSC stemness and its survival niche. This review covers the cellular and molecular mechanisms underlying the symbiotic interactions between CSCs and immune cells and how such heterotypic signaling maintains a tumor-promoting ecosystem and informs therapeutic strategies intercepting this co-dependency. 2021-01-05 /pmc/articles/PMC7839836/ /pubmed/33406434 http://dx.doi.org/10.1016/j.celrep.2020.108597 Text en This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Chen, Peiwen Hsu, Wen-Hao Han, Jincheng Xia, Yan DePinho, Ronald A. Cancer Stemness Meets Immunity: From Mechanism to Therapy |
title | Cancer Stemness Meets Immunity: From Mechanism to Therapy |
title_full | Cancer Stemness Meets Immunity: From Mechanism to Therapy |
title_fullStr | Cancer Stemness Meets Immunity: From Mechanism to Therapy |
title_full_unstemmed | Cancer Stemness Meets Immunity: From Mechanism to Therapy |
title_short | Cancer Stemness Meets Immunity: From Mechanism to Therapy |
title_sort | cancer stemness meets immunity: from mechanism to therapy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7839836/ https://www.ncbi.nlm.nih.gov/pubmed/33406434 http://dx.doi.org/10.1016/j.celrep.2020.108597 |
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