Cargando…
Not so WEE: Targeting G(2)/M to kill mesothelioma cells
It has been known for many years that manipulation of cell cycle checkpoint function represents one approach by which the toxicity of chemotherapy and of ionizing radiation can be increased in tumor cells.(1)(-)(3) In particular, abrogation of the G(2)/M checkpoint has been shown to enhance the leth...
Autor principal: | |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Landes Bioscience
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3979810/ https://www.ncbi.nlm.nih.gov/pubmed/24496096 http://dx.doi.org/10.4161/cbt.27851 |
_version_ | 1782310770419171328 |
---|---|
author | Dent, Paul |
author_facet | Dent, Paul |
author_sort | Dent, Paul |
collection | PubMed |
description | It has been known for many years that manipulation of cell cycle checkpoint function represents one approach by which the toxicity of chemotherapy and of ionizing radiation can be increased in tumor cells.(1)(-)(3) In particular, abrogation of the G(2)/M checkpoint has been shown to enhance the lethality of a wide range of toxic stresses.(1)(-)(3) Inhibition of the G(2)/M checkpoint after chemotherapy/irradiation would result in tumor cells entering mitosis with damaged DNA, which would in turn result in loss of clonogenic survival (i.e., a lethal mitosis). |
format | Online Article Text |
id | pubmed-3979810 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Landes Bioscience |
record_format | MEDLINE/PubMed |
spelling | pubmed-39798102015-04-01 Not so WEE: Targeting G(2)/M to kill mesothelioma cells Dent, Paul Cancer Biol Ther Commentary It has been known for many years that manipulation of cell cycle checkpoint function represents one approach by which the toxicity of chemotherapy and of ionizing radiation can be increased in tumor cells.(1)(-)(3) In particular, abrogation of the G(2)/M checkpoint has been shown to enhance the lethality of a wide range of toxic stresses.(1)(-)(3) Inhibition of the G(2)/M checkpoint after chemotherapy/irradiation would result in tumor cells entering mitosis with damaged DNA, which would in turn result in loss of clonogenic survival (i.e., a lethal mitosis). Landes Bioscience 2014-04-01 2014-02-04 /pmc/articles/PMC3979810/ /pubmed/24496096 http://dx.doi.org/10.4161/cbt.27851 Text en Copyright © 2014 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited. |
spellingShingle | Commentary Dent, Paul Not so WEE: Targeting G(2)/M to kill mesothelioma cells |
title | Not so WEE: Targeting G(2)/M to kill mesothelioma cells |
title_full | Not so WEE: Targeting G(2)/M to kill mesothelioma cells |
title_fullStr | Not so WEE: Targeting G(2)/M to kill mesothelioma cells |
title_full_unstemmed | Not so WEE: Targeting G(2)/M to kill mesothelioma cells |
title_short | Not so WEE: Targeting G(2)/M to kill mesothelioma cells |
title_sort | not so wee: targeting g(2)/m to kill mesothelioma cells |
topic | Commentary |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3979810/ https://www.ncbi.nlm.nih.gov/pubmed/24496096 http://dx.doi.org/10.4161/cbt.27851 |
work_keys_str_mv | AT dentpaul notsoweetargetingg2mtokillmesotheliomacells |