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Oncogenic senescence: a multi-functional perspective
Cellular senescence is defined as an irreversible growth arrest with the acquisition of a distinctive secretome. The growth arrest is a potent anticancer mechanism whereas the secretome facilitates wound healing, tissue repair, and development. The senescence response has also become increasingly re...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5432366/ https://www.ncbi.nlm.nih.gov/pubmed/28416761 http://dx.doi.org/10.18632/oncotarget.15742 |
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author | Baker, Darren J. Alimirah, Fatouma van Deursen, Jan M. Campisi, Judith Hildesheim, Jeffrey |
author_facet | Baker, Darren J. Alimirah, Fatouma van Deursen, Jan M. Campisi, Judith Hildesheim, Jeffrey |
author_sort | Baker, Darren J. |
collection | PubMed |
description | Cellular senescence is defined as an irreversible growth arrest with the acquisition of a distinctive secretome. The growth arrest is a potent anticancer mechanism whereas the secretome facilitates wound healing, tissue repair, and development. The senescence response has also become increasingly recognized as an important contributor to aging and age-related diseases, including cancer. Although oncogenic mutations are capable of inducing a beneficial senescence response that prevents the growth of premalignant cells and promotes cancer immune-surveillance, the secretome of senescent cells also includes factors with pro-tumorigenic properties. On June 23(rd) and 24(th), 2016, the Division of Cancer Biology of the National Cancer Institute sponsored a workshop to discuss the complex role of cellular senescence in tumorigenesis with the goal to define the major challenges and opportunities within this important field of cancer research. Additionally, it was noted how the development of novel tools and technologies are required to accelerate research into a mechanistic understanding of senescent cells in carcinogenesis in order to overcome the current limitations in this exciting, yet ill-defined area. |
format | Online Article Text |
id | pubmed-5432366 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-54323662017-05-17 Oncogenic senescence: a multi-functional perspective Baker, Darren J. Alimirah, Fatouma van Deursen, Jan M. Campisi, Judith Hildesheim, Jeffrey Oncotarget Meeting Report Cellular senescence is defined as an irreversible growth arrest with the acquisition of a distinctive secretome. The growth arrest is a potent anticancer mechanism whereas the secretome facilitates wound healing, tissue repair, and development. The senescence response has also become increasingly recognized as an important contributor to aging and age-related diseases, including cancer. Although oncogenic mutations are capable of inducing a beneficial senescence response that prevents the growth of premalignant cells and promotes cancer immune-surveillance, the secretome of senescent cells also includes factors with pro-tumorigenic properties. On June 23(rd) and 24(th), 2016, the Division of Cancer Biology of the National Cancer Institute sponsored a workshop to discuss the complex role of cellular senescence in tumorigenesis with the goal to define the major challenges and opportunities within this important field of cancer research. Additionally, it was noted how the development of novel tools and technologies are required to accelerate research into a mechanistic understanding of senescent cells in carcinogenesis in order to overcome the current limitations in this exciting, yet ill-defined area. Impact Journals LLC 2017-02-25 /pmc/articles/PMC5432366/ /pubmed/28416761 http://dx.doi.org/10.18632/oncotarget.15742 Text en Copyright: © 2017 Baker et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Meeting Report Baker, Darren J. Alimirah, Fatouma van Deursen, Jan M. Campisi, Judith Hildesheim, Jeffrey Oncogenic senescence: a multi-functional perspective |
title | Oncogenic senescence: a multi-functional perspective |
title_full | Oncogenic senescence: a multi-functional perspective |
title_fullStr | Oncogenic senescence: a multi-functional perspective |
title_full_unstemmed | Oncogenic senescence: a multi-functional perspective |
title_short | Oncogenic senescence: a multi-functional perspective |
title_sort | oncogenic senescence: a multi-functional perspective |
topic | Meeting Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5432366/ https://www.ncbi.nlm.nih.gov/pubmed/28416761 http://dx.doi.org/10.18632/oncotarget.15742 |
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