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Review
. 2024 Feb 1;16(2):e53431.
doi: 10.7759/cureus.53431. eCollection 2024 Feb.

HIV-Encoded Gene Therapy as Anti-cancer Therapeutics: A Narrative Review

Affiliations
Review

HIV-Encoded Gene Therapy as Anti-cancer Therapeutics: A Narrative Review

Pachamuthu Balakrishnan et al. Cureus. .

Abstract

Recently, there has been interest in using viruses as cancer treatments. Oncolytic virology was founded by scientists who noticed that viruses might preferentially lyse cancer cells over healthy ones. Oncolytic virotherapy has similar obstacles as other treatment approaches, gaining entry into the specific tumour cell, encountering antiviral immune responses, off-target infection and many other unfavourable circumstances in the tumour microenvironment, and a lack of unique therapeutic and predictive biomarkers. However, oncolytic viruses have emerged as the main players in the biological treatment for cancer with the use of vectors such as human adenoviruses in oncolytic virotherapy. Recent large-scale research has shown that other viruses, such as the measles virus and the herpes simplex virus (HSV), may potentially be viable options for cancer treatment. The FDA has cleared T-VEC, an HSV-based oncolytic virus, for use in biological cancer treatment after its successful completion of human clinical trials. Furthermore, the measles virus vaccine strain has shown remarkable outcomes in pre-clinical and clinical testing. The use of such modified viruses in biological cancer treatment holds promise for groundbreaking discoveries in the field of cancer research because of their therapeutic effectiveness, fewer side effects, and safety. Several other newer approaches have been used in recent years. HIV-encoded proteins are also hypothesized to promote mitochondrial homeostasis causing bystander-induced apoptosis. We provide an overview of the most recent developments in the clinical use of oncolytic virus-based biological cancer treatment in this study. This evaluation also assesses the advantages and disadvantages of the viral candidates and provides insight into their potential in the future.

Keywords: head and neck neoplasms; hiv aids; oncolytic virus therapy; oral cavity squamous cell carcinoma; viral vector.

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Conflict of interest statement

The authors have declared that no competing interests exist.

Figures

Figure 1
Figure 1. Challenges and benefits associated with the genetically modified viruses used in oncolytic viral therapy.
Image Credit: Author Pachamuthu Balakrishnan

References

    1. Global cancer statistics 2020: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. Sung H, Ferlay J, Siegel RL, Laversanne M, Soerjomataram I, Jemal A, Bray F. CA Cancer J Clin. 2021;71:209–249. - PubMed
    1. Oncolytic viruses for cancer therapy: barriers and recent advances. Zheng M, Huang J, Tong A, Yang H. Mol Ther Oncolytics. 2019;15:234–247. - PMC - PubMed
    1. Oncolytic viral therapy and the immune system: a double-edged sword against cancer. Marelli G, Howells A, Lemoine NR, Wang Y. Front Immunol. 2018;9:866. - PMC - PubMed
    1. Oncolytic activity of HF10 in head and neck squamous cell carcinomas. Esaki S, Goshima F, Ozaki H, et al. Cancer Gene Ther. 2020;27:585–598. - PMC - PubMed
    1. Efficient delivery and replication of oncolytic virus for successful treatment of head and neck cancer. Hamada M, Yura Y. Int J Mol Sci. 2020;21:7073. - PMC - PubMed

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