Research output: Contribution to journal › Article › peer-review
Evaluating the efficiency of the tumor-initiating stem cells eradication strategy on the example of ascite form of mouse gepatocarcinoma G-29. / Potter, E. A.; Ritter, G. S.; Dolgova, E. V. et al.
In: Voprosy Onkologii, Vol. 64, No. 6, 01.01.2018, p. 818-829.Research output: Contribution to journal › Article › peer-review
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TY - JOUR
T1 - Evaluating the efficiency of the tumor-initiating stem cells eradication strategy on the example of ascite form of mouse gepatocarcinoma G-29
AU - Potter, E. A.
AU - Ritter, G. S.
AU - Dolgova, E. V.
AU - Proskurina, A. S.
AU - Kisaretova, P. E.
AU - Efremov, Y. R.
AU - Nikolin, V. P.
AU - Popova, N. A.
AU - Taranov, O. S.
AU - Ostanin, A. A.
AU - Chernych, E. R.
AU - Sidorov, S. V.
AU - Kolchanov, N. A.
AU - Bogachev, S. S.
PY - 2018/1/1
Y1 - 2018/1/1
N2 - Previously, we identified a treatment regimen ("3+1") to synchronize and eradicate solid and ascites forms of murine Krebs-2 tumor. Using a similar strategy, we attempted to narrow down the treatment conditions for mouse hepatocarcinoma G-29 that can be passaged in mice as either ascites or solid grafts. We successfully developed the protocol that allowed elimination of the primary ascites. Our results indicate that the "3+1" treatment protocol wherein the final doses of cyclophosphamide and double-stranded DNA preparation are given on days 6 or 11 had the greatest therapeutic effect. Mean survival time was 36 days in treated mice vs 27 days in untreated controls. We further demonstrate that tightly scheduled cyclophosphamide treatment was in itself highly inhibitory to the growing G-29 ascites. It has been shown that in the case of ascitic form of G-29 tumor after synergistic action of cytostatic and double-stranded DNA preparation, secondary ascites arises following the appearance of peritoneal carcinomatous solid formation and, apparently, is its derivative.
AB - Previously, we identified a treatment regimen ("3+1") to synchronize and eradicate solid and ascites forms of murine Krebs-2 tumor. Using a similar strategy, we attempted to narrow down the treatment conditions for mouse hepatocarcinoma G-29 that can be passaged in mice as either ascites or solid grafts. We successfully developed the protocol that allowed elimination of the primary ascites. Our results indicate that the "3+1" treatment protocol wherein the final doses of cyclophosphamide and double-stranded DNA preparation are given on days 6 or 11 had the greatest therapeutic effect. Mean survival time was 36 days in treated mice vs 27 days in untreated controls. We further demonstrate that tightly scheduled cyclophosphamide treatment was in itself highly inhibitory to the growing G-29 ascites. It has been shown that in the case of ascitic form of G-29 tumor after synergistic action of cytostatic and double-stranded DNA preparation, secondary ascites arises following the appearance of peritoneal carcinomatous solid formation and, apparently, is its derivative.
KW - Cyclophosphamide
KW - Double-stranded DNA
KW - Hepatocarcinoma G-29
KW - Secondary ascites
UR - http://www.scopus.com/inward/record.url?scp=85063515995&partnerID=8YFLogxK
M3 - Article
AN - SCOPUS:85063515995
VL - 64
SP - 818
EP - 829
JO - Voprosy Onkologii
JF - Voprosy Onkologii
SN - 0507-3758
IS - 6
ER -
ID: 19038682