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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2018
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.
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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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