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Apoptosis, ageing and cancer susceptibility
We have previously shown that peripheral blood lymphocytes (PBL) from individuals carrying a germline TP53 mutation show a dramatically reduced apoptotic response to radiation. As part of a study of this phenomenon, we also investigated apoptotic response in a series of breast cancer patients lackin...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2003
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2377171/ https://www.ncbi.nlm.nih.gov/pubmed/12592359 http://dx.doi.org/10.1038/sj.bjc.6600767 |
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author | Camplejohn, R S Gilchrist, R Easton, D McKenzie-Edwards, E Barnes, D M Eccles, D M Ardern-Jones, A Hodgson, S V Duddy, P M Eeles, R A |
author_facet | Camplejohn, R S Gilchrist, R Easton, D McKenzie-Edwards, E Barnes, D M Eccles, D M Ardern-Jones, A Hodgson, S V Duddy, P M Eeles, R A |
author_sort | Camplejohn, R S |
collection | PubMed |
description | We have previously shown that peripheral blood lymphocytes (PBL) from individuals carrying a germline TP53 mutation show a dramatically reduced apoptotic response to radiation. As part of a study of this phenomenon, we also investigated apoptotic response in a series of breast cancer patients lacking TP53 mutations and in a control group of individuals without cancer. There was a significant reduction in mean apoptotic response with increasing age in all groups. These findings are consistent with a number of studies in rodents, which have demonstrated a reduction in DNA damage-induced apoptosis with increasing age. In addition, after adjusting for age, breast cancer patients showed significantly reduced apoptotic responses compared with normal controls (P=0.002). The odds ratio for breast cancer in women with an apoptotic response of <35%, compared with women with a response of >49%, was 6.42 (95% CI 1.68–24.6). The data further support the hypothesis that a reduction in apoptotic response to DNA damage with increasing age may play a significant role in the age-related increase in cancer. |
format | Text |
id | pubmed-2377171 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2003 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23771712009-09-10 Apoptosis, ageing and cancer susceptibility Camplejohn, R S Gilchrist, R Easton, D McKenzie-Edwards, E Barnes, D M Eccles, D M Ardern-Jones, A Hodgson, S V Duddy, P M Eeles, R A Br J Cancer Clinical We have previously shown that peripheral blood lymphocytes (PBL) from individuals carrying a germline TP53 mutation show a dramatically reduced apoptotic response to radiation. As part of a study of this phenomenon, we also investigated apoptotic response in a series of breast cancer patients lacking TP53 mutations and in a control group of individuals without cancer. There was a significant reduction in mean apoptotic response with increasing age in all groups. These findings are consistent with a number of studies in rodents, which have demonstrated a reduction in DNA damage-induced apoptosis with increasing age. In addition, after adjusting for age, breast cancer patients showed significantly reduced apoptotic responses compared with normal controls (P=0.002). The odds ratio for breast cancer in women with an apoptotic response of <35%, compared with women with a response of >49%, was 6.42 (95% CI 1.68–24.6). The data further support the hypothesis that a reduction in apoptotic response to DNA damage with increasing age may play a significant role in the age-related increase in cancer. Nature Publishing Group 2003-02-24 2003-02-18 /pmc/articles/PMC2377171/ /pubmed/12592359 http://dx.doi.org/10.1038/sj.bjc.6600767 Text en Copyright © 2003 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Clinical Camplejohn, R S Gilchrist, R Easton, D McKenzie-Edwards, E Barnes, D M Eccles, D M Ardern-Jones, A Hodgson, S V Duddy, P M Eeles, R A Apoptosis, ageing and cancer susceptibility |
title | Apoptosis, ageing and cancer susceptibility |
title_full | Apoptosis, ageing and cancer susceptibility |
title_fullStr | Apoptosis, ageing and cancer susceptibility |
title_full_unstemmed | Apoptosis, ageing and cancer susceptibility |
title_short | Apoptosis, ageing and cancer susceptibility |
title_sort | apoptosis, ageing and cancer susceptibility |
topic | Clinical |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2377171/ https://www.ncbi.nlm.nih.gov/pubmed/12592359 http://dx.doi.org/10.1038/sj.bjc.6600767 |
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