Virotherapy: From single agents to combinatorial treatments.
Alkylating Agents
/ therapeutic use
Antibiotics, Antineoplastic
/ therapeutic use
Antibodies, Monoclonal
/ therapeutic use
Antimetabolites, Antineoplastic
/ therapeutic use
Antimitotic Agents
/ therapeutic use
Combined Modality Therapy
/ methods
Histone Deacetylase Inhibitors
/ therapeutic use
Humans
Immunotherapy
/ methods
Neoplasms
/ genetics
Oncolytic Virotherapy
/ methods
Oncolytic Viruses
/ genetics
Platinum Compounds
/ therapeutic use
Protein Kinase Inhibitors
/ therapeutic use
Topoisomerase Inhibitors
/ therapeutic use
Tumor Microenvironment
/ drug effects
Immunotherapy
Oncolytic virus
Journal
Biochemical pharmacology
ISSN: 1873-2968
Titre abrégé: Biochem Pharmacol
Pays: England
ID NLM: 0101032
Informations de publication
Date de publication:
07 2020
07 2020
Historique:
received:
18
02
2020
accepted:
16
04
2020
pubmed:
25
4
2020
medline:
2
12
2020
entrez:
25
4
2020
Statut:
ppublish
Résumé
Virotherpay is emerging as a promising strategy against cancer, and three oncolytic viruses (OVs) have gained approval in different countries for the treatment of several cancer types. Beyond the capability to selectively infect, replicate and lyse cancer cells, OVs act through a multitude of events, including modification of the tumour micro/macro-environment as well as a complex modulation of the anti-tumour immune response by activation of danger signals and immunogenic cell death pathways. Most OVs show limited effects, depending on the viral platform and the interactions with the host. OVs used as monotherapy only in a minority of patients elicited a full response. Better outcomes were obtained using OVs in combination with other treatments, such as immune therapy or chemotherapy, suggesting that the full potential of OVs can be unleashed in combination with other treatment modalities. Here, we report the main described combination of OVs with conventional chemotherapeutic agents: platinum salts, mitotic inhibitors, anthracyclines and other antibiotics, anti-metabolites, alkylating agents and topoisomerase inhibitors. Additionally, our work provides an overview of OV combination with targeted therapies: histone deacetylase inhibitors, kinase inhibitors, monoclonal antibodies, inhibitors of DNA repair, inhibitors of the proteasome complex and statins that demonstrated enhanced OV anti-neoplastic activity. Although further studies are required to assess the best combinations to translate the results in the clinic, it is clear that combined therapies, acting with complementary mechanisms of action might be useful to target cancer lesions resistant to currently available treatments.
Identifiants
pubmed: 32330494
pii: S0006-2952(20)30214-8
doi: 10.1016/j.bcp.2020.113986
pii:
doi:
Substances chimiques
Alkylating Agents
0
Antibiotics, Antineoplastic
0
Antibodies, Monoclonal
0
Antimetabolites, Antineoplastic
0
Antimitotic Agents
0
Histone Deacetylase Inhibitors
0
Platinum Compounds
0
Protein Kinase Inhibitors
0
Topoisomerase Inhibitors
0
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
113986Informations de copyright
Copyright © 2020. Published by Elsevier Inc.