Combination of microRNA and suicide gene for targeting Glioblastoma: Inducing apoptosis and significantly suppressing tumor growth in vivo.

5-Fluorocytosine Apoptosis Cytosine deaminase Glioblastoma miR-34a

Journal

Heliyon
ISSN: 2405-8440
Titre abrégé: Heliyon
Pays: England
ID NLM: 101672560

Informations de publication

Date de publication:
15 Sep 2024
Historique:
received: 10 03 2024
revised: 12 08 2024
accepted: 22 08 2024
medline: 17 9 2024
pubmed: 17 9 2024
entrez: 17 9 2024
Statut: epublish

Résumé

Glioblastoma (GBM), a grade IV brain tumor, presents a severe challenge in treatment and eradication due to its high genetic variability and the existence of stem-like cells with self-renewal potential. Conventional therapies fall short of preventing recurrence and fail to extend the median survival of patients significantly. However, the emergence of gene therapy, which has recently obtained significant clinical outcomes, brings hope. It has the potential to be a suitable strategy for the treatment of GBM. Notably, microRNAs (miRNAs) have been noticed as critical players in the development and progress of GBM. The combined usage of hsa-miR-34a and Cytosine Deaminase (CD) suicide gene and 5-fluorocytosine (5FC) prodrug caused cytotoxicity against U87MG Glioma cells

Identifiants

pubmed: 39286083
doi: 10.1016/j.heliyon.2024.e37041
pii: S2405-8440(24)13072-1
pmc: PMC11403485
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e37041

Informations de copyright

© 2024 Published by Elsevier Ltd.

Déclaration de conflit d'intérêts

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Zahra Fekrirad (Z)

Department of Microbiology, School of Biology, College of Science, University of Tehran, Tehran, Iran.
Department of Biology, Faculty of Basic Sciences, Shahed University, Tehran, Iran.

Milad Gharedaghi (M)

Department of Microbiology, School of Biology, College of Science, University of Tehran, Tehran, Iran.

Fatemeh Saadatpour (F)

Department of Microbiology, School of Biology, College of Science, University of Tehran, Tehran, Iran.

Zahra Asghari Molabashi (ZA)

Department of Plant Molecular Biotechnology, National Institute of Genetic Engineering and Biotechnology, Tehran, Iran.

Ameneh Rezayof (A)

Neuroscience Lab, Department of Animal Biology, School of Biology, College of Science, University of Tehran, Tehran, Iran.

Alireza Korourian (A)

Oncopathology Research Center, Iran University of Medical Sciences, Tehran, Iran.

Masoud Soleimani (M)

Department of Hematology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran.

Ehsan Arefian (E)

Department of Microbiology, School of Biology, College of Science, University of Tehran, Tehran, Iran.
Department of Stem Cells Technology and Tissue Regeneration, School of Biology, College of Science, University of Tehran, Tehran, Iran.

Classifications MeSH