Cargando…

The ratio of single- to double-strand DNA breaks and their absolute values determine cell death pathway

Bleomycin is a cytotoxic antibiotic that generates DNA double-strand breaks (DSB) and DNA single-strand breaks (SSB). It is possible to introduce known quantities of bleomycin molecules into cells. Low amounts kill the cells by a slow process termed mitotic cell death, while high amounts produce a f...

Descripción completa

Detalles Bibliográficos
Autores principales: Tounekti, O, Kenani, A, Foray, N, Orlowski, S, Mir, L M
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2001
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2363894/
https://www.ncbi.nlm.nih.gov/pubmed/11336481
http://dx.doi.org/10.1054/bjoc.2001.1786
_version_ 1782153818151059456
author Tounekti, O
Kenani, A
Foray, N
Orlowski, S
Mir, L M
author_facet Tounekti, O
Kenani, A
Foray, N
Orlowski, S
Mir, L M
author_sort Tounekti, O
collection PubMed
description Bleomycin is a cytotoxic antibiotic that generates DNA double-strand breaks (DSB) and DNA single-strand breaks (SSB). It is possible to introduce known quantities of bleomycin molecules into cells. Low amounts kill the cells by a slow process termed mitotic cell death, while high amounts produce a fast process that has been termed pseudoapoptosis. We previously showed that these types of cell death are a direct consequence of the DSB generated by bleomycin. Here, we use deglyco-bleomycin, a bleomycin derivative lacking the carbohydrate moiety. Although this molecule performs the same nucleophilic attacks on DNA as bleomycin, we show that deglyco-bleomycin is at least 100 times less toxic to Chinese hamster fibroblasts than bleomycin. In fact, deglyco-bleomycin treatment results in apoptosis induction. In contrast, however, deglyco-bleomycin was found to generate almost exclusively SSB. Our results suggest that more than 150 000 SSB per cell are required to trigger apoptosis in Chinese hamster fibroblasts and that SSB are 300 times less toxic than DSB. Taken together with previous studies on bleomycin, our data demonstrates that cells can die by apoptosis, mitotic cell death, or pseudoapoptosis, depending on the number of DNA breaks and on the ratio of SSB to DSB. © 2001 Cancer Research Campaign http://www.bjcancer.com
format Text
id pubmed-2363894
institution National Center for Biotechnology Information
language English
publishDate 2001
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-23638942009-09-10 The ratio of single- to double-strand DNA breaks and their absolute values determine cell death pathway Tounekti, O Kenani, A Foray, N Orlowski, S Mir, L M Br J Cancer Regular Article Bleomycin is a cytotoxic antibiotic that generates DNA double-strand breaks (DSB) and DNA single-strand breaks (SSB). It is possible to introduce known quantities of bleomycin molecules into cells. Low amounts kill the cells by a slow process termed mitotic cell death, while high amounts produce a fast process that has been termed pseudoapoptosis. We previously showed that these types of cell death are a direct consequence of the DSB generated by bleomycin. Here, we use deglyco-bleomycin, a bleomycin derivative lacking the carbohydrate moiety. Although this molecule performs the same nucleophilic attacks on DNA as bleomycin, we show that deglyco-bleomycin is at least 100 times less toxic to Chinese hamster fibroblasts than bleomycin. In fact, deglyco-bleomycin treatment results in apoptosis induction. In contrast, however, deglyco-bleomycin was found to generate almost exclusively SSB. Our results suggest that more than 150 000 SSB per cell are required to trigger apoptosis in Chinese hamster fibroblasts and that SSB are 300 times less toxic than DSB. Taken together with previous studies on bleomycin, our data demonstrates that cells can die by apoptosis, mitotic cell death, or pseudoapoptosis, depending on the number of DNA breaks and on the ratio of SSB to DSB. © 2001 Cancer Research Campaign http://www.bjcancer.com Nature Publishing Group 2001-05 /pmc/articles/PMC2363894/ /pubmed/11336481 http://dx.doi.org/10.1054/bjoc.2001.1786 Text en Copyright © 2001 Cancer Research Campaign 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 Regular Article
Tounekti, O
Kenani, A
Foray, N
Orlowski, S
Mir, L M
The ratio of single- to double-strand DNA breaks and their absolute values determine cell death pathway
title The ratio of single- to double-strand DNA breaks and their absolute values determine cell death pathway
title_full The ratio of single- to double-strand DNA breaks and their absolute values determine cell death pathway
title_fullStr The ratio of single- to double-strand DNA breaks and their absolute values determine cell death pathway
title_full_unstemmed The ratio of single- to double-strand DNA breaks and their absolute values determine cell death pathway
title_short The ratio of single- to double-strand DNA breaks and their absolute values determine cell death pathway
title_sort ratio of single- to double-strand dna breaks and their absolute values determine cell death pathway
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2363894/
https://www.ncbi.nlm.nih.gov/pubmed/11336481
http://dx.doi.org/10.1054/bjoc.2001.1786
work_keys_str_mv AT tounektio theratioofsingletodoublestranddnabreaksandtheirabsolutevaluesdeterminecelldeathpathway
AT kenania theratioofsingletodoublestranddnabreaksandtheirabsolutevaluesdeterminecelldeathpathway
AT forayn theratioofsingletodoublestranddnabreaksandtheirabsolutevaluesdeterminecelldeathpathway
AT orlowskis theratioofsingletodoublestranddnabreaksandtheirabsolutevaluesdeterminecelldeathpathway
AT mirlm theratioofsingletodoublestranddnabreaksandtheirabsolutevaluesdeterminecelldeathpathway
AT tounektio ratioofsingletodoublestranddnabreaksandtheirabsolutevaluesdeterminecelldeathpathway
AT kenania ratioofsingletodoublestranddnabreaksandtheirabsolutevaluesdeterminecelldeathpathway
AT forayn ratioofsingletodoublestranddnabreaksandtheirabsolutevaluesdeterminecelldeathpathway
AT orlowskis ratioofsingletodoublestranddnabreaksandtheirabsolutevaluesdeterminecelldeathpathway
AT mirlm ratioofsingletodoublestranddnabreaksandtheirabsolutevaluesdeterminecelldeathpathway