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Evaluation of a strategy for tumor-initiating stem cell eradication in primary human glioblastoma cultures as a model. / Dolgova, E. V.; Proskurina, A. S.; Potter, E. A. и др.

в: Вавиловский журнал генетики и селекции, Том 22, № 7, 01.01.2018, стр. 825-836.

Результаты исследований: Научные публикации в периодических изданияхстатьяРецензирование

Harvard

Dolgova, EV, Proskurina, AS, Potter, EA, Tyrinova, TV, Taranov, OS, Efremov, YR, Orishchenko, KE, Mishinov, SV, Stupak, VV, Ostanin, AA, Chernykh, ER & Bogachev, SS 2018, 'Evaluation of a strategy for tumor-initiating stem cell eradication in primary human glioblastoma cultures as a model', Вавиловский журнал генетики и селекции, Том. 22, № 7, стр. 825-836. https://doi.org/10.18699/VJ18.31-o

APA

Dolgova, E. V., Proskurina, A. S., Potter, E. A., Tyrinova, T. V., Taranov, O. S., Efremov, Y. R., Orishchenko, K. E., Mishinov, S. V., Stupak, V. V., Ostanin, A. A., Chernykh, E. R., & Bogachev, S. S. (2018). Evaluation of a strategy for tumor-initiating stem cell eradication in primary human glioblastoma cultures as a model. Вавиловский журнал генетики и селекции, 22(7), 825-836. https://doi.org/10.18699/VJ18.31-o

Vancouver

Dolgova EV, Proskurina AS, Potter EA, Tyrinova TV, Taranov OS, Efremov YR и др. Evaluation of a strategy for tumor-initiating stem cell eradication in primary human glioblastoma cultures as a model. Вавиловский журнал генетики и селекции. 2018 янв. 1;22(7):825-836. doi: 10.18699/VJ18.31-o

Author

Dolgova, E. V. ; Proskurina, A. S. ; Potter, E. A. и др. / Evaluation of a strategy for tumor-initiating stem cell eradication in primary human glioblastoma cultures as a model. в: Вавиловский журнал генетики и селекции. 2018 ; Том 22, № 7. стр. 825-836.

BibTeX

@article{f9555b3839b14749b41f2257636721f2,
title = "Evaluation of a strategy for tumor-initiating stem cell eradication in primary human glioblastoma cultures as a model",
abstract = "Primary cultures of human glioblastoma were obtained from the surgical material of patients K. (female, 61 years, Ds: relapse of glioblastoma) and Zh. (female, 60 years, Ds: relapse of glioblastoma). The effectiveness of a new therapeutic approach aimed at destroying the cancer cell community was evaluated on the primary cell lines of human glioblastoma culture by employing a new strategy of tumor-initiating stem cell synchronization and a domestic strategy of their eradication “3+1”. The key elements of the strategy were the following indicator results: (1) evaluation of the presence of tumor-initiating stem cells in a population of cells from analyzed cultures by their ability to internalize double-stranded labeled DNA (TAMRA+ cells); (2) determination of the reference time points of the repair cycle of DNA interstrand cross-links induced by cross-linking cytostatic mitomycin C; (3) evaluation of cell cycle synchronization; (4) determination of the time (day after therapy initiation) when TAMRA+ cells were synchronously present in phase G1/S of the cell cycle, sensitive to the therapy; and (5) establishment of the TAMRA+ (tumor-initiating stem cells) eradication schedule. The cultures were treated with cross-linking cytostatic mitomycin C and a compositional DNA preparation. After the treatments, cell division slows down, and the cultures degrade. The K cell line completely degraded within 30 days of observation. The cell number of the Zh culture fell to nearly one-third of the starting value by day 15 of observation. on day 15, this indicator constituted 1/7.45 for mitomycin C and 1/10.28 for mitomycin C + DNA with reference to the control. The main target of the mitomycin C + DNA regimen was TAMRA+ tumor-initiating stem cells of the glioblastoma cell populations. The action of mitomycin C alone or in the combination with DNA demonstrated effective elimination of TAMRA+ tumor-initiating stem cells and the whole primary cultures of human glioblastomas.",
keywords = "Glioblastoma, Mytomycin C, Primary cell line, TAMRA-fluorochrom, Tumor-initiating stem cells",
author = "Dolgova, {E. V.} and Proskurina, {A. S.} and Potter, {E. A.} and Tyrinova, {T. V.} and Taranov, {O. S.} and Efremov, {Ya R.} and Orishchenko, {K. E.} and Mishinov, {S. V.} and Stupak, {V. V.} and Ostanin, {A. A.} and Chernykh, {E. R.} and Bogachev, {S. S.}",
note = "Publisher Copyright: {\textcopyright} AUTHoRS, 2018 Copyright: Copyright 2018 Elsevier B.V., All rights reserved.",
year = "2018",
month = jan,
day = "1",
doi = "10.18699/VJ18.31-o",
language = "English",
volume = "22",
pages = "825--836",
journal = "Вавиловский журнал генетики и селекции",
issn = "2500-0462",
publisher = "Institute of Cytology and Genetics of Siberian Branch of the Russian Academy of Sciences",
number = "7",

}

RIS

TY - JOUR

T1 - Evaluation of a strategy for tumor-initiating stem cell eradication in primary human glioblastoma cultures as a model

AU - Dolgova, E. V.

AU - Proskurina, A. S.

AU - Potter, E. A.

AU - Tyrinova, T. V.

AU - Taranov, O. S.

AU - Efremov, Ya R.

AU - Orishchenko, K. E.

AU - Mishinov, S. V.

AU - Stupak, V. V.

AU - Ostanin, A. A.

AU - Chernykh, E. R.

AU - Bogachev, S. S.

N1 - Publisher Copyright: © AUTHoRS, 2018 Copyright: Copyright 2018 Elsevier B.V., All rights reserved.

PY - 2018/1/1

Y1 - 2018/1/1

N2 - Primary cultures of human glioblastoma were obtained from the surgical material of patients K. (female, 61 years, Ds: relapse of glioblastoma) and Zh. (female, 60 years, Ds: relapse of glioblastoma). The effectiveness of a new therapeutic approach aimed at destroying the cancer cell community was evaluated on the primary cell lines of human glioblastoma culture by employing a new strategy of tumor-initiating stem cell synchronization and a domestic strategy of their eradication “3+1”. The key elements of the strategy were the following indicator results: (1) evaluation of the presence of tumor-initiating stem cells in a population of cells from analyzed cultures by their ability to internalize double-stranded labeled DNA (TAMRA+ cells); (2) determination of the reference time points of the repair cycle of DNA interstrand cross-links induced by cross-linking cytostatic mitomycin C; (3) evaluation of cell cycle synchronization; (4) determination of the time (day after therapy initiation) when TAMRA+ cells were synchronously present in phase G1/S of the cell cycle, sensitive to the therapy; and (5) establishment of the TAMRA+ (tumor-initiating stem cells) eradication schedule. The cultures were treated with cross-linking cytostatic mitomycin C and a compositional DNA preparation. After the treatments, cell division slows down, and the cultures degrade. The K cell line completely degraded within 30 days of observation. The cell number of the Zh culture fell to nearly one-third of the starting value by day 15 of observation. on day 15, this indicator constituted 1/7.45 for mitomycin C and 1/10.28 for mitomycin C + DNA with reference to the control. The main target of the mitomycin C + DNA regimen was TAMRA+ tumor-initiating stem cells of the glioblastoma cell populations. The action of mitomycin C alone or in the combination with DNA demonstrated effective elimination of TAMRA+ tumor-initiating stem cells and the whole primary cultures of human glioblastomas.

AB - Primary cultures of human glioblastoma were obtained from the surgical material of patients K. (female, 61 years, Ds: relapse of glioblastoma) and Zh. (female, 60 years, Ds: relapse of glioblastoma). The effectiveness of a new therapeutic approach aimed at destroying the cancer cell community was evaluated on the primary cell lines of human glioblastoma culture by employing a new strategy of tumor-initiating stem cell synchronization and a domestic strategy of their eradication “3+1”. The key elements of the strategy were the following indicator results: (1) evaluation of the presence of tumor-initiating stem cells in a population of cells from analyzed cultures by their ability to internalize double-stranded labeled DNA (TAMRA+ cells); (2) determination of the reference time points of the repair cycle of DNA interstrand cross-links induced by cross-linking cytostatic mitomycin C; (3) evaluation of cell cycle synchronization; (4) determination of the time (day after therapy initiation) when TAMRA+ cells were synchronously present in phase G1/S of the cell cycle, sensitive to the therapy; and (5) establishment of the TAMRA+ (tumor-initiating stem cells) eradication schedule. The cultures were treated with cross-linking cytostatic mitomycin C and a compositional DNA preparation. After the treatments, cell division slows down, and the cultures degrade. The K cell line completely degraded within 30 days of observation. The cell number of the Zh culture fell to nearly one-third of the starting value by day 15 of observation. on day 15, this indicator constituted 1/7.45 for mitomycin C and 1/10.28 for mitomycin C + DNA with reference to the control. The main target of the mitomycin C + DNA regimen was TAMRA+ tumor-initiating stem cells of the glioblastoma cell populations. The action of mitomycin C alone or in the combination with DNA demonstrated effective elimination of TAMRA+ tumor-initiating stem cells and the whole primary cultures of human glioblastomas.

KW - Glioblastoma

KW - Mytomycin C

KW - Primary cell line

KW - TAMRA-fluorochrom

KW - Tumor-initiating stem cells

UR - http://www.scopus.com/inward/record.url?scp=85057112705&partnerID=8YFLogxK

U2 - 10.18699/VJ18.31-o

DO - 10.18699/VJ18.31-o

M3 - Article

AN - SCOPUS:85057112705

VL - 22

SP - 825

EP - 836

JO - Вавиловский журнал генетики и селекции

JF - Вавиловский журнал генетики и селекции

SN - 2500-0462

IS - 7

ER -

ID: 17563377