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Efficacy of a new cancer treatment strategy based on eradication of tumor-initiating stem cells in a mouse model of Krebs-2 solid adenocarcinoma
Krebs-2 solid carcinoma was cured using a new “3+1” strategy for eradication of Krebs-2 tumor-initiating stem cells. This strategy was based on synchronization of these cells in a treatment-sensitive phase of the cell cycle. The synchronization mechanism, subsequent destruction of Krebs-2 tumor-init...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6033367/ https://www.ncbi.nlm.nih.gov/pubmed/29983875 http://dx.doi.org/10.18632/oncotarget.25503 |
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author | Potter, Ekaterina A. Proskurina, Anastasia S. Ritter, Genrikh S. Dolgova, Evgenia V. Nikolin, Valeriy P. Popova, Nelly A. Taranov, Oleg S. Efremov, Yaroslav R. Bayborodin, Sergey I. Ostanin, Aleksandr A. Chernykh, Elena R. Kolchanov, Nikolay A. Bogachev, Sergey S. |
author_facet | Potter, Ekaterina A. Proskurina, Anastasia S. Ritter, Genrikh S. Dolgova, Evgenia V. Nikolin, Valeriy P. Popova, Nelly A. Taranov, Oleg S. Efremov, Yaroslav R. Bayborodin, Sergey I. Ostanin, Aleksandr A. Chernykh, Elena R. Kolchanov, Nikolay A. Bogachev, Sergey S. |
author_sort | Potter, Ekaterina A. |
collection | PubMed |
description | Krebs-2 solid carcinoma was cured using a new “3+1” strategy for eradication of Krebs-2 tumor-initiating stem cells. This strategy was based on synchronization of these cells in a treatment-sensitive phase of the cell cycle. The synchronization mechanism, subsequent destruction of Krebs-2 tumor-initiating stem cells, and cure of mice from a solid graft were found to depend on the temporal profile of the interstrand cross-link repair cycle. Also, the temporal profile of the Krebs-2 interstrand repair cycle was found to have a pronounced seasonal cyclicity at the place of experiments (Novosibirsk, Russia). As a result, the therapeutic effect that is based on application of the described strategy, originally developed for the “winter repair cycle” (November−April), is completely eliminated in the summer period (June−September). We conclude that оne of the possible and the likeliest reasons for our failure to observe the therapeutic effects was the seasonal cyclicity in the duration of the interstrand repair cycle, the parameter that is central to our strategy. |
format | Online Article Text |
id | pubmed-6033367 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-60333672018-07-08 Efficacy of a new cancer treatment strategy based on eradication of tumor-initiating stem cells in a mouse model of Krebs-2 solid adenocarcinoma Potter, Ekaterina A. Proskurina, Anastasia S. Ritter, Genrikh S. Dolgova, Evgenia V. Nikolin, Valeriy P. Popova, Nelly A. Taranov, Oleg S. Efremov, Yaroslav R. Bayborodin, Sergey I. Ostanin, Aleksandr A. Chernykh, Elena R. Kolchanov, Nikolay A. Bogachev, Sergey S. Oncotarget Research Paper Krebs-2 solid carcinoma was cured using a new “3+1” strategy for eradication of Krebs-2 tumor-initiating stem cells. This strategy was based on synchronization of these cells in a treatment-sensitive phase of the cell cycle. The synchronization mechanism, subsequent destruction of Krebs-2 tumor-initiating stem cells, and cure of mice from a solid graft were found to depend on the temporal profile of the interstrand cross-link repair cycle. Also, the temporal profile of the Krebs-2 interstrand repair cycle was found to have a pronounced seasonal cyclicity at the place of experiments (Novosibirsk, Russia). As a result, the therapeutic effect that is based on application of the described strategy, originally developed for the “winter repair cycle” (November−April), is completely eliminated in the summer period (June−September). We conclude that оne of the possible and the likeliest reasons for our failure to observe the therapeutic effects was the seasonal cyclicity in the duration of the interstrand repair cycle, the parameter that is central to our strategy. Impact Journals LLC 2018-06-19 /pmc/articles/PMC6033367/ /pubmed/29983875 http://dx.doi.org/10.18632/oncotarget.25503 Text en Copyright: © 2018 Potter et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Potter, Ekaterina A. Proskurina, Anastasia S. Ritter, Genrikh S. Dolgova, Evgenia V. Nikolin, Valeriy P. Popova, Nelly A. Taranov, Oleg S. Efremov, Yaroslav R. Bayborodin, Sergey I. Ostanin, Aleksandr A. Chernykh, Elena R. Kolchanov, Nikolay A. Bogachev, Sergey S. Efficacy of a new cancer treatment strategy based on eradication of tumor-initiating stem cells in a mouse model of Krebs-2 solid adenocarcinoma |
title | Efficacy of a new cancer treatment strategy based on eradication of tumor-initiating stem cells in a mouse model of Krebs-2 solid adenocarcinoma |
title_full | Efficacy of a new cancer treatment strategy based on eradication of tumor-initiating stem cells in a mouse model of Krebs-2 solid adenocarcinoma |
title_fullStr | Efficacy of a new cancer treatment strategy based on eradication of tumor-initiating stem cells in a mouse model of Krebs-2 solid adenocarcinoma |
title_full_unstemmed | Efficacy of a new cancer treatment strategy based on eradication of tumor-initiating stem cells in a mouse model of Krebs-2 solid adenocarcinoma |
title_short | Efficacy of a new cancer treatment strategy based on eradication of tumor-initiating stem cells in a mouse model of Krebs-2 solid adenocarcinoma |
title_sort | efficacy of a new cancer treatment strategy based on eradication of tumor-initiating stem cells in a mouse model of krebs-2 solid adenocarcinoma |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6033367/ https://www.ncbi.nlm.nih.gov/pubmed/29983875 http://dx.doi.org/10.18632/oncotarget.25503 |
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