The antitumor effect of oncolytic respiratory syncytial virus via the tumor necrosis factor-alpha induction and ROS-bax-mediated mechanisms.


Journal

BMC cancer
ISSN: 1471-2407
Titre abrégé: BMC Cancer
Pays: England
ID NLM: 100967800

Informations de publication

Date de publication:
28 Aug 2023
Historique:
received: 18 06 2023
accepted: 22 08 2023
medline: 31 8 2023
pubmed: 29 8 2023
entrez: 28 8 2023
Statut: epublish

Résumé

Cervical cancer represents one of the most prevalent cancers among women worldwide, particularly in low- and middle-income nations. Oncolytic viruses (OVs) can infect cancer cells selectively and lethally without harming normal cells. Respiratory syncytial virus (RSV) is an oncolytic virus for anticancer therapy because of its propensity to multiply within tumor cells. This research aimed to assess the in vitro antitumor activities and molecular basis processes of the oncolytic RSV-A2 on the TC-1 cancer cells as a model for HPV‑related cervical cancers. Cellular proliferation (MTT) and lactate dehydrogenase (LDH) release assays were used to investigate the catalytic impacts of RSV-A2 by the ELISA method. Real-time PCR and flow cytometry assays were utilized to assess apoptosis, autophagy, intracellular concentrations of reactive oxygen species (ROS), and cell cycle inhibition. Our MTT and LDH results demonstrated that TC-1 cell viability after oncolytic RSV-A2 treatment was MOI-dependently and altered significantly with increasing RSV-A2 virus multiplicity of infection (MOI). Other findings showed that the RSV-A2 potentially resulted in apoptosis and autophagy induction, caspase-3 activation, ROS generation, and cell cycle inhibition in the TC-1 cell line. Real-time PCR assay revealed that RSV-A2 infection significantly elevated the Bax and decreased the Bcl2 expression. The results indicated that oncolytic RSV-A2 has cytotoxic and inhibiting effects on HPV-associated cervical cancer cells. Our findings revealed that RSV-A2 is a promising treatment candidate for cervical cancer.

Sections du résumé

BACKGROUND BACKGROUND
Cervical cancer represents one of the most prevalent cancers among women worldwide, particularly in low- and middle-income nations. Oncolytic viruses (OVs) can infect cancer cells selectively and lethally without harming normal cells. Respiratory syncytial virus (RSV) is an oncolytic virus for anticancer therapy because of its propensity to multiply within tumor cells. This research aimed to assess the in vitro antitumor activities and molecular basis processes of the oncolytic RSV-A2 on the TC-1 cancer cells as a model for HPV‑related cervical cancers.
METHODS METHODS
Cellular proliferation (MTT) and lactate dehydrogenase (LDH) release assays were used to investigate the catalytic impacts of RSV-A2 by the ELISA method. Real-time PCR and flow cytometry assays were utilized to assess apoptosis, autophagy, intracellular concentrations of reactive oxygen species (ROS), and cell cycle inhibition.
RESULTS RESULTS
Our MTT and LDH results demonstrated that TC-1 cell viability after oncolytic RSV-A2 treatment was MOI-dependently and altered significantly with increasing RSV-A2 virus multiplicity of infection (MOI). Other findings showed that the RSV-A2 potentially resulted in apoptosis and autophagy induction, caspase-3 activation, ROS generation, and cell cycle inhibition in the TC-1 cell line. Real-time PCR assay revealed that RSV-A2 infection significantly elevated the Bax and decreased the Bcl2 expression.
CONCLUSIONS CONCLUSIONS
The results indicated that oncolytic RSV-A2 has cytotoxic and inhibiting effects on HPV-associated cervical cancer cells. Our findings revealed that RSV-A2 is a promising treatment candidate for cervical cancer.

Identifiants

pubmed: 37641004
doi: 10.1186/s12885-023-11326-y
pii: 10.1186/s12885-023-11326-y
pmc: PMC10464077
doi:

Substances chimiques

Reactive Oxygen Species 0
Tumor Necrosis Factor-alpha 0
bcl-2-Associated X Protein 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

803

Subventions

Organisme : Tehran University of Medical Sciences and Health Services
ID : 99-1-99-42374

Informations de copyright

© 2023. BioMed Central Ltd., part of Springer Nature.

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Auteurs

Mehdi Samadi (M)

Virology Department, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.

Talat Mokhtari-Azad (T)

Virology Department, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.

Ahmad Nejati (A)

Virology Department, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.

Zahra Norooz-Babaei (Z)

Virology Department, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.

Abbas Rahimi Foroushani (AR)

Department of Statistics and Epidemiology, School of Public Health, Tehran University of medical sciences, Tehran, Iran.

Mohammad Reza Haghshenas (MR)

Department of Microbiology, Molecular, and Cell-Biology Research Center, Faculty of Medicine, Mazandaran University of Medical Sciences, Sari, Iran.

Fatemeh Adjaminejad (F)

Virology Department, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.

Hedieh Zargaran (H)

Department of Influenza and Other Respiratory Viruses, Pasteur Institute of Iran, Tehran, Iran.

Vahid Salimi (V)

Virology Department, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran. vahidsalimii@gmail.com.

Amir Ghaemi (A)

Department of Influenza and Other Respiratory Viruses, Pasteur Institute of Iran, Tehran, Iran. ghaem_amir@yahoo.com.

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