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Damage-associated molecular patterns in cancer: A double-edged sword
Damage-associated molecular patterns (DAMPs) are released in response to cell death and stress, and are potent triggers of sterile inflammation. Recent evidence suggests that DAMPs may also have a key role in the development of cancer as well as in the host response to cytotoxic anti-tumor therapy....
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5119456/ https://www.ncbi.nlm.nih.gov/pubmed/27086930 http://dx.doi.org/10.1038/onc.2016.104 |
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author | Hernandez, Celine Huebener, Peter Schwabe, Robert F. |
author_facet | Hernandez, Celine Huebener, Peter Schwabe, Robert F. |
author_sort | Hernandez, Celine |
collection | PubMed |
description | Damage-associated molecular patterns (DAMPs) are released in response to cell death and stress, and are potent triggers of sterile inflammation. Recent evidence suggests that DAMPs may also have a key role in the development of cancer as well as in the host response to cytotoxic anti-tumor therapy. As such, DAMPs may exert protective functions by alerting the immune system to the presence of dying tumor cells, thereby triggering immunogenic tumor cell death. On the other hand, cell death and release of DAMPs may also trigger chronic inflammation and thereby promote the development or progression of tumors. Here, we will review the contribution of candidate DAMPs and their receptors and discuss the evidence for DAMPs as tumor-promoting and anti-tumor effectors as well as unsolved questions such as DAMP release from non-tumor cells as well as the existence of tumor-specific DAMPs. |
format | Online Article Text |
id | pubmed-5119456 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
record_format | MEDLINE/PubMed |
spelling | pubmed-51194562016-11-23 Damage-associated molecular patterns in cancer: A double-edged sword Hernandez, Celine Huebener, Peter Schwabe, Robert F. Oncogene Article Damage-associated molecular patterns (DAMPs) are released in response to cell death and stress, and are potent triggers of sterile inflammation. Recent evidence suggests that DAMPs may also have a key role in the development of cancer as well as in the host response to cytotoxic anti-tumor therapy. As such, DAMPs may exert protective functions by alerting the immune system to the presence of dying tumor cells, thereby triggering immunogenic tumor cell death. On the other hand, cell death and release of DAMPs may also trigger chronic inflammation and thereby promote the development or progression of tumors. Here, we will review the contribution of candidate DAMPs and their receptors and discuss the evidence for DAMPs as tumor-promoting and anti-tumor effectors as well as unsolved questions such as DAMP release from non-tumor cells as well as the existence of tumor-specific DAMPs. 2016-04-18 2016-11-17 /pmc/articles/PMC5119456/ /pubmed/27086930 http://dx.doi.org/10.1038/onc.2016.104 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Hernandez, Celine Huebener, Peter Schwabe, Robert F. Damage-associated molecular patterns in cancer: A double-edged sword |
title | Damage-associated molecular patterns in cancer: A double-edged
sword |
title_full | Damage-associated molecular patterns in cancer: A double-edged
sword |
title_fullStr | Damage-associated molecular patterns in cancer: A double-edged
sword |
title_full_unstemmed | Damage-associated molecular patterns in cancer: A double-edged
sword |
title_short | Damage-associated molecular patterns in cancer: A double-edged
sword |
title_sort | damage-associated molecular patterns in cancer: a double-edged
sword |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5119456/ https://www.ncbi.nlm.nih.gov/pubmed/27086930 http://dx.doi.org/10.1038/onc.2016.104 |
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