Anticancer Activity of Measles-Mumps-Rubella MMR Vaccine Viruses against Glioblastoma

被引:2
|
作者
Khalid, Zumama [1 ]
Coco, Simona [2 ]
Ullah, Nadir [1 ]
Pulliero, Alessandra [1 ]
Cortese, Katia [3 ]
Varesano, Serena [2 ]
Orsi, Andrea [1 ,2 ]
Izzotti, Alberto [2 ,3 ]
机构
[1] Univ Genoa, Dept Hlth Sci, Via Pastore 1, Genoa 16132, Italy
[2] IRCCS Osped Policlin San Martino, Largo Rosanna Benzi 10, I-16132 Genoa, Italy
[3] Univ Genoa, Dept Expt Med, I-16132 Genoa, Italy
关键词
oncolytic viruses; virotherapy; glioblastoma; MMR vaccine; PHASE-I TRIAL; CONDITIONALLY-REPLICATIVE ADENOVIRUS; RECURRENT MALIGNANT GLIOMAS; HERPES-SIMPLEX-VIRUS; SUICIDE GENE-THERAPY; ONCOLYTIC ADENOVIRUS; CARCINOEMBRYONIC ANTIGEN; ANTITUMOR IMMUNITY; CLINICAL-TRIAL; SOLID TUMORS;
D O I
10.3390/cancers15174304
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Simple Summary This research has been suggested after a gap was found in the previous literature, and our hypothesis of the MMR vaccine being an oncolytic virus. The present study has been designed to study and cover the followings objectives: to evaluate the therapeutic effect of the measles virus vaccine strains on cancer, through wet-lab experimental analysis; and to study the previous literature on the application of oncolytic viruses. Our findings highlight the therapeutic potential of the MMR vaccine strain for the treatment of glioblastoma (GBM).Abstract Background: Oncolytic viruses (OVs) have been utilized since 1990s for targeted cancer treatment. Our study examined the Measles-Mumps-Rubella (MMR) vaccine's cancer-killing potency against Glioblastoma (GBM), a therapy-resistant, aggressive cancer type. Methodology: We used GBM cell lines, primary GBM cells, and normal mice microglial cells, to assess the MMR vaccine's efficacy through cell viability, cell cycle analysis, intracellular viral load via RT-PCR, and Transmission Electron Microscopy (TEM). Results: After 72 h of MMR treatment, GBM cell lines and primary GBM cells exhibited significant viability reduction compared to untreated cells. Conversely, normal microglial cells showed only minor changes in viability and morphology. Intracellular viral load tests indicated GBM cells' increased sensitivity to MMR viruses compared to normal cells. The cell cycle study also revealed measles and mumps viruses' crucial role in cytopathic effects, with the rubella virus causing cell cycle arrest. Conclusion: Herein the reported results demonstrate the anti-cancer activity of the MMR vaccine against GBM cells. Accordingly, the MMR vaccine warrants further study as a potential new tool for GBM therapy and relapse prevention. Therapeutic potential of the MMR vaccine has been found to be promising in earlier studies as well.
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页数:27
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