EVALUATING THE EFFECTIVENESS OF THE TUMOR-INITIATING STEM CELLS ERADICATION STRATEGY ON THE EXAMPLE OF HUMAN GLIOBLASTOMA CELL LINE U87

2019 ◽  
Vol 65 (6) ◽  
pp. 904-919
Author(s):  
Yevgeniya Dolgova ◽  
Yekaterina Potter ◽  
Anastasiya Proskurina ◽  
Valeriy Nikolin ◽  
Nelli Popova ◽  
...  

The effectiveness of the new therapeutic approach aimed at the destruction of the cancer cell community was evaluated on the immortalized human glioblastoma cell line U87. Initially, the reference elements of a new strategy for eradication of tumor-initiating stem cells were characterized. The main points of the strategy were as follows. 1) Evaluation of the TAMRA+ (tumor-initiating stem cells) presence in the population of U87 culture cells. 2) Determination of the reference time points of the DNA interstrand cross-links repair, induced by cross-linking cytostatics mitomycin C. 3) Determination of the day after initiation of therapy when TAMRA+ cells accumulate and are synchronously present in the G1/S sensitive for the treatment phase of the cell cycle. Based on the data obtained, a therapeutic regimen aimed at eradicating TAMRA+ cells (tumor-initiating stem cells) was identified. Treatment of the culture was carried out by cross-linking cytostatic mitomycin C and complex DNA preparation. Transplantation experiments showed that high experimental doses of mitomycin C (20 μg/ml) totally destroy transplantation potential of U87 cells. Diminution of mitomycin C to therapeutic doses (5 μg/ ml) clearly demonstrated effect of complex double-stranded DNA preparation to reducing of U87 tumorigenic potential. These fully confirmed the concept of developed cancer treatment technology.

2008 ◽  
Vol 265 (1) ◽  
pp. 124-134 ◽  
Author(s):  
Shi-cang Yu ◽  
Yi-fang Ping ◽  
Liang Yi ◽  
Zhi-hua Zhou ◽  
Jian-hong Chen ◽  
...  

2021 ◽  
Vol 22 (11) ◽  
pp. 5557
Author(s):  
Tao-Chieh Yang ◽  
Shih-Jung Liu ◽  
Wei-Lun Lo ◽  
Shu-Mei Chen ◽  
Ya-Ling Tang ◽  
...  

Glioblastoma multiforme (GBM) has remained one of the most lethal and challenging cancers to treat. Previous studies have shown encouraging results when irinotecan was used in combination with temozolomide (TMZ) for treating GBM. However, irinotecan has a narrow therapeutic index: a slight dose increase in irinotecan can induce toxicities that outweigh its therapeutic benefits. SN-38 is the active metabolite of irinotecan that accounts for both its anti-tumor efficacy and toxicity. In our previous paper, we showed that SN-38 embedded into 50:50 biodegradable poly[(d,l)-lactide-co-glycolide] (PLGA) microparticles (SMPs) provides an efficient delivery and sustained release of SN-38 from SMPs in the brain tissues of rats. These properties of SMPs give them potential for therapeutic application due to their high efficacy and low toxicity. In this study, we tested the anti-tumor activity of SMP-based interstitial chemotherapy combined with TMZ using TMZ-resistant human glioblastoma cell line-derived xenograft models. Our data suggest that treatment in which SMPs are combined with TMZ reduces tumor growth and extends survival in mice bearing xenograft tumors derived from both TMZ-resistant and TMZ-sensitive human glioblastoma cell lines. Our findings demonstrate that combining SMPs with TMZ may have potential as a promising strategy for the treatment of GBM.


Author(s):  
W.A.S. Ferreira ◽  
C.K.N. Amorim ◽  
R.R. Burbano ◽  
R.A.R. Villacis ◽  
F.A. Marchi ◽  
...  

1995 ◽  
Vol 84 (2) ◽  
pp. 142
Author(s):  
Dan Fults ◽  
Carolyn A. Pedone ◽  
Xiao Lin Zhu ◽  
Briana J. Williams ◽  
Emma Jones ◽  
...  

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