The viral approach to breast cancer immunotherapy.


Journal

Journal of cellular physiology
ISSN: 1097-4652
Titre abrégé: J Cell Physiol
Pays: United States
ID NLM: 0050222

Informations de publication

Date de publication:
02 2019
Historique:
received: 05 03 2018
accepted: 05 07 2018
pubmed: 28 8 2018
medline: 18 12 2019
entrez: 28 8 2018
Statut: ppublish

Résumé

Despite years of intensive research, breast cancer remains the leading cause of death in women worldwide. New technologies including oncolytic virus therapies, virus, and phage display are among the most powerful and advanced methods that have emerged in recent years with potential applications in cancer prevention and treatment. Oncolytic virus therapy is an interesting strategy for cancer treatment. Presently, a number of viruses from different virus families are under laboratory and clinical investigation as oncolytic therapeutics. Oncolytic viruses (OVs) have been shown to be able to induce and initiate a systemic antitumor immune response. The possibility of application of a multimodal therapy using a combination of the OV therapy with immune checkpoint inhibitors and cancer antigen vaccination holds a great promise in the future of cancer immunotherapy. Display of immunologic peptides on bacterial viruses (bacteriophages) is also increasingly being considered as a new and strong cancer vaccine delivery strategy. In phage display immunotherapy, a peptide or protein antigen is presented by genetic fusions to the phage coat proteins, and the phage construct formulation acts as a protective or preventive vaccine against cancer. In our laboratory, we have recently tested a few peptides (E75, AE37, and GP2) derived from HER2/neu proto-oncogene as vaccine delivery modalities for the treatment of TUBO breast cancer xenograft tumors of BALB/c mice. Here, in this paper, we discuss the latest advancements in the applications of OVs and bacterial viruses display systems as new and advanced modalities in cancer immune therapeutics.

Identifiants

pubmed: 30146692
doi: 10.1002/jcp.27150
doi:

Substances chimiques

Antineoplastic Agents, Immunological 0
Cancer Vaccines 0
MAS1 protein, human 0
Proto-Oncogene Mas 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

1257-1267

Informations de copyright

© 2018 Wiley Periodicals, Inc.

Auteurs

Atefeh Arab (A)

Biotechnology Research Center, Pharmaceutical Technology Institute, Mashhad University of Medical Sciences, Mashhad, Iran.

Nima Behravan (N)

Pharmaspring Inc, Richmond Hill, ON, Canada.

Atefeh Razazn (A)

Biotechnology Research Center, Pharmaceutical Technology Institute, Mashhad University of Medical Sciences, Mashhad, Iran.

Nastaran Barati (N)

Biotechnology Research Center, Pharmaceutical Technology Institute, Mashhad University of Medical Sciences, Mashhad, Iran.

Fatemeh Mosaffa (F)

Biotechnology Research Center, Pharmaceutical Technology Institute, Mashhad University of Medical Sciences, Mashhad, Iran.

Jessica Nicastro (J)

School of Pharmacy, University of Waterloo, Waterloo, ON, Canada.
Waterloo Institute of Nanotechnology, University of Waterloo, Waterloo, ON, Canada.

Roderick Slavcev (R)

School of Pharmacy, University of Waterloo, Waterloo, ON, Canada.
Waterloo Institute of Nanotechnology, University of Waterloo, Waterloo, ON, Canada.
Mediphage Bioceuticals, Inc., MaRS Centre, Toronto, ON, Canada.

Javad Behravan (J)

Biotechnology Research Center, Pharmaceutical Technology Institute, Mashhad University of Medical Sciences, Mashhad, Iran.
Mediphage Bioceuticals, Inc., MaRS Centre, Toronto, ON, Canada.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH