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Cancer Stem Cells: Emergent Nature of Tumor Emergency

A functional analysis of 167 genes overexpressed in Krebs-2 tumor initiating cells was performed. In the first part of the study, the genes were analyzed for their belonging to one or more of the three groups, which represent the three major phenotypic manifestation of malignancy of cancer cells, na...

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Autores principales: Efremov, Yaroslav R., Proskurina, Anastasia S., Potter, Ekaterina A., Dolgova, Evgenia V., Efremova, Oksana V., Taranov, Oleg S., Ostanin, Aleksandr A., Chernykh, Elena R., Kolchanov, Nikolay A., Bogachev, Sergey S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6250818/
https://www.ncbi.nlm.nih.gov/pubmed/30505319
http://dx.doi.org/10.3389/fgene.2018.00544
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author Efremov, Yaroslav R.
Proskurina, Anastasia S.
Potter, Ekaterina A.
Dolgova, Evgenia V.
Efremova, Oksana V.
Taranov, Oleg S.
Ostanin, Aleksandr A.
Chernykh, Elena R.
Kolchanov, Nikolay A.
Bogachev, Sergey S.
author_facet Efremov, Yaroslav R.
Proskurina, Anastasia S.
Potter, Ekaterina A.
Dolgova, Evgenia V.
Efremova, Oksana V.
Taranov, Oleg S.
Ostanin, Aleksandr A.
Chernykh, Elena R.
Kolchanov, Nikolay A.
Bogachev, Sergey S.
author_sort Efremov, Yaroslav R.
collection PubMed
description A functional analysis of 167 genes overexpressed in Krebs-2 tumor initiating cells was performed. In the first part of the study, the genes were analyzed for their belonging to one or more of the three groups, which represent the three major phenotypic manifestation of malignancy of cancer cells, namely (1) proliferative self-sufficiency, (2) invasive growth and metastasis, and (3) multiple drug resistance. 96 genes out of 167 were identified as possible contributors to at least one of these fundamental properties. It was also found that substantial part of these genes are also known as genes responsible for formation and/or maintenance of the stemness of normal pluri-/multipotent stem cells. These results suggest that the malignancy is simply the ability to maintain the stem cell specific genes expression profile, and, as a consequence, the stemness itself regardless of the controlling effect of stem niches. In the second part of the study, three stress factors combined into the single concept of “generalized cellular stress,” which are assumed to activate the expression of these genes, were defined. In addition, possible mechanisms for such activation were identified. The data obtained suggest the existence of a mechanism for the de novo formation of a pluripotent/stem phenotype in the subpopulation of “committed” tumor cells.
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spelling pubmed-62508182018-11-30 Cancer Stem Cells: Emergent Nature of Tumor Emergency Efremov, Yaroslav R. Proskurina, Anastasia S. Potter, Ekaterina A. Dolgova, Evgenia V. Efremova, Oksana V. Taranov, Oleg S. Ostanin, Aleksandr A. Chernykh, Elena R. Kolchanov, Nikolay A. Bogachev, Sergey S. Front Genet Genetics A functional analysis of 167 genes overexpressed in Krebs-2 tumor initiating cells was performed. In the first part of the study, the genes were analyzed for their belonging to one or more of the three groups, which represent the three major phenotypic manifestation of malignancy of cancer cells, namely (1) proliferative self-sufficiency, (2) invasive growth and metastasis, and (3) multiple drug resistance. 96 genes out of 167 were identified as possible contributors to at least one of these fundamental properties. It was also found that substantial part of these genes are also known as genes responsible for formation and/or maintenance of the stemness of normal pluri-/multipotent stem cells. These results suggest that the malignancy is simply the ability to maintain the stem cell specific genes expression profile, and, as a consequence, the stemness itself regardless of the controlling effect of stem niches. In the second part of the study, three stress factors combined into the single concept of “generalized cellular stress,” which are assumed to activate the expression of these genes, were defined. In addition, possible mechanisms for such activation were identified. The data obtained suggest the existence of a mechanism for the de novo formation of a pluripotent/stem phenotype in the subpopulation of “committed” tumor cells. Frontiers Media S.A. 2018-11-16 /pmc/articles/PMC6250818/ /pubmed/30505319 http://dx.doi.org/10.3389/fgene.2018.00544 Text en Copyright © 2018 Efremov, Proskurina, Potter, Dolgova, Efremova, Taranov, Ostanin, Chernykh, Kolchanov and Bogachev. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Efremov, Yaroslav R.
Proskurina, Anastasia S.
Potter, Ekaterina A.
Dolgova, Evgenia V.
Efremova, Oksana V.
Taranov, Oleg S.
Ostanin, Aleksandr A.
Chernykh, Elena R.
Kolchanov, Nikolay A.
Bogachev, Sergey S.
Cancer Stem Cells: Emergent Nature of Tumor Emergency
title Cancer Stem Cells: Emergent Nature of Tumor Emergency
title_full Cancer Stem Cells: Emergent Nature of Tumor Emergency
title_fullStr Cancer Stem Cells: Emergent Nature of Tumor Emergency
title_full_unstemmed Cancer Stem Cells: Emergent Nature of Tumor Emergency
title_short Cancer Stem Cells: Emergent Nature of Tumor Emergency
title_sort cancer stem cells: emergent nature of tumor emergency
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6250818/
https://www.ncbi.nlm.nih.gov/pubmed/30505319
http://dx.doi.org/10.3389/fgene.2018.00544
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