scholarly journals Different Recurrence and Growth Pattern of Gliomatous Foci after Mesenchymal Stem Cell Harbouring the Herpes Simplex Thymidine Kinase Gene Transplantation in Multifocal Glioblastoma Multiform: A Clinical Case Report

Author(s):  
Saeed Oraee Yazdani ◽  
Mohammadhosein Akhlaghpasand ◽  
Maryam Golmohammadi ◽  
Fatemeh Rostami ◽  
Gelareh Shokri ◽  
...  

Abstract Background: Glioblastoma multiform (GBM) as a malignant brain tumor has poor prognosis despite the current therapies. Suicide gene therapy is one of the most widespread cancer gene therapies which requires mRNA encoding a pro-drug activating enzyme transduced into the vector such as Mesenchymal Stem Cells (MSCs) that injects into the tumor tissue and leads to tumor suppression. Case presentation: In this case report, the authors describe a 37-year-old man with two obvious foci of glioblastoma multiform at left frontal and left parietal lobes. After the resection of the foci, the patient received stem cell-mediated herpes simplex virus thymidine kinase (HSV-TK) gene at frontal focus of tumor besides ganciclovir as prodrug for 14 days after injection. Then he was followed up with regular magnetic resonance imaging (MRI). The growth and recurrence pattern of foci was assessed. After the injection on Feb 09, 2019, the patient’s follow-up revealed recurrence of parietal focus on Dec 19, 2019; however, frontal focus had a slight and unremarkable enhancement. Until our last radiological follow-up (on Mar 18, 2020) left frontal focus had no prominent recurrence and the size of the left parietal focus increased and extended to the contralateral hemisphere through the corpus callosum. Eventually patient has passed away on July 16, 2020 (PFS=293 days, OS=657 days).Conclusions: It seems that the gliomatous focus that undergone administration of bone marrow MSC containing the HSV-TK gene, had a different pattern of growth and recurrence compared to a non-treated one.

Oncology ◽  
2005 ◽  
Vol 69 (6) ◽  
pp. 503-508 ◽  
Author(s):  
Shaoyi Li ◽  
Tsutomu Tokuyama ◽  
Junkoh Yamamoto ◽  
Masayo Koide ◽  
Naoki Yokota ◽  
...  

1979 ◽  
Vol 7 (4) ◽  
pp. 859-878 ◽  
Author(s):  
N.M. Wilkie ◽  
J.B. Clements ◽  
W. Boll ◽  
N. Mantei ◽  
D. Lonsdale ◽  
...  

1982 ◽  
Vol 2 (4) ◽  
pp. 426-436 ◽  
Author(s):  
C J Tabin ◽  
J W Hoffmann ◽  
S P Goff ◽  
R A Weinberg

We investigated the feasibility of using retroviruses as vectors for transferring DNA sequences into animal cells. The thymidine kinase (tk) gene of herpes simplex virus was chosen as a convenient model. The internal BamHI fragments of a DNA clone of Moloney leukemia virus (MLV) were replaced with a purified BamHI DNA segment containing the tk gene. Chimeric genomes were created carrying the tk insert in both orientations relative to the MLV sequence. Each was transfected into TK- cells along with MLV helper virus, and TK+ colonies were obtained by selection in the presence of hypoxanthine, aminopterin, and thymidine (HAT). Virus collected from TK+-transformed, MLV producer cells passed the TK+ phenotype to TK- cells. Nonproducer cells were isolated, and TK+ transducing virus was subsequently rescued from them. The chimeric virus showed single-hit kinetics in infections. Virion and cellular RNA and cellular DNA from infected cells were all shown to contain sequences which hybridized to both MLV- and tk-specific probes. The sizes of these sequences were consistent with those predicted for the chimeric virus. In all respects studied, the chimeric MLV-tk virus behaved like known replication-defective retroviruses. These experiments suggest great general applicability of retroviruses as eucaryotic vectors.


Pancreas ◽  
1997 ◽  
Vol 15 (1) ◽  
pp. 25-34 ◽  
Author(s):  
Andreas Block ◽  
Shu-Hsia Chen ◽  
Ken-Ichiro Kosai ◽  
Milton Finegold ◽  
Savio L. C. Woo

1996 ◽  
Vol 106 (6) ◽  
pp. 1163-1168 ◽  
Author(s):  
Bernd Bonnekoh ◽  
David A. Greenhalgh ◽  
Donnie S. Bundman ◽  
Ken-ichiro Kosai ◽  
Shu-Hsia Chen ◽  
...  

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