The role of viruses in cancer development versus cancer therapy: An oncological perspective.
Dr Hossein JavidAlireza Sharbaf MashhadShaghayegh YazdaniMahsa Akbari OryaniSanaz AkbariNastaran RezagholinejadMahboubeh TajaldiniMehdi Karimi-ShahriPublished in: Cancer medicine (2023)
Despite great medical advances, oncological research is still looking for novel therapeutic approaches due to the limitation of conventional therapeutic agents. Virotherapy is one of these new emerging therapeutic approaches that attract attention with their widespread applications. Virotherapy use lives oncolytic viruses or genetically engineered viruses that selectively infect the tumor cells, replicate, and disrupt the cancerous cells that also induce their anticancer activity by stimulating the host antitumor immune response. Moreover, viruses are widely used as target delivery vectors for specifically delivering different genes, therapeutic agents, and immune-stimulating agents. In addition to having antitumor activity by themselves in combination with conventional therapeutic agents like immune therapy and chemotherapy, Virotherapy agents also elicit promising outcomes. Therefore, in addition to their promising result in monotherapy use, virotherapy agents can also be used in combination with conventional cancer therapy, epigenetic modulators, and even microRNAs without any cross-resistance, which allows the patient not to be deprived of her routine medicine. Still, this combination therapy reduces the adverse effect of the conventional therapies. All together suggest that virotherapy agents as novel potential agents in the field of cancer therapy.
Keyphrases
- cancer therapy
- combination therapy
- immune response
- drug delivery
- healthcare
- prostate cancer
- type diabetes
- randomized controlled trial
- small molecule
- squamous cell carcinoma
- emergency department
- clinical trial
- induced apoptosis
- signaling pathway
- metabolic syndrome
- radiation therapy
- oxidative stress
- genome wide
- radical prostatectomy
- toll like receptor
- mesenchymal stem cells
- open label
- cell cycle arrest
- robot assisted
- insulin resistance
- squamous cell
- drug induced