» Articles » PMID: 24062768

Exploiting Tumor Epigenetics to Improve Oncolytic Virotherapy

Overview
Journal Front Genet
Date 2013 Sep 25
PMID 24062768
Citations 11
Authors
Affiliations
Soon will be listed here.
Abstract

Oncolytic viruses (OVs) comprise a versatile and multi-mechanistic therapeutic platform in the growing arsenal of anticancer biologics. These replicating therapeutics find favorable conditions in the tumor niche, characterized among others by increased metabolism, reduced anti-tumor/antiviral immunity, and disorganized vasculature. Through a self-amplification that is dependent on multiple cancer-specific defects, these agents exhibit remarkable tumor selectivity. With several OVs completing or entering Phase III clinical evaluation, their therapeutic potential as well as the challenges ahead are increasingly clear. One key hurdle is tumor heterogeneity, which results in variations in the ability of tumors to support productive infection by OVs and to induce adaptive anti-tumor immunity. To this end, mounting evidence suggests tumor epigenetics may play a key role. This review will focus on the epigenetic landscape of tumors and how it relates to OV infection. Therapeutic strategies aiming to exploit the epigenetic identity of tumors in order to improve OV therapy are also discussed.

Citing Articles

The Advances in the Development of Epigenetic Modifications Therapeutic Drugs Delivery Systems.

Li T, Chen Y, Li S Int J Nanomedicine. 2024; 19:10623-10637.

PMID: 39445155 PMC: 11498046. DOI: 10.2147/IJN.S480095.


Low-dose decitabine enhances the efficacy of viral cancer vaccines for immunotherapy.

Russo S, Feola S, Feodoroff M, Chiaro J, Antignani G, Fusciello M Mol Ther Oncol. 2024; 32(1):200766.

PMID: 38596301 PMC: 10869747. DOI: 10.1016/j.omton.2024.200766.


Improving cancer immunotherapy by rationally combining oncolytic virus with modulators targeting key signaling pathways.

Zhu Z, McGray A, Jiang W, Lu B, Kalinski P, Guo Z Mol Cancer. 2022; 21(1):196.

PMID: 36221123 PMC: 9554963. DOI: 10.1186/s12943-022-01664-z.


Ovarian Cancer Immunotherapy: Preclinical Models and Emerging Therapeutics.

McCloskey C, Rodriguez G, Galpin K, Vanderhyden B Cancers (Basel). 2018; 10(8).

PMID: 30049987 PMC: 6115831. DOI: 10.3390/cancers10080244.


Tumor Restrictions to Oncolytic Virus.

Vaha-Koskela M, Hinkkanen A Biomedicines. 2017; 2(2):163-194.

PMID: 28548066 PMC: 5423468. DOI: 10.3390/biomedicines2020163.


References
1.
Bannister A, Kouzarides T . Regulation of chromatin by histone modifications. Cell Res. 2011; 21(3):381-95. PMC: 3193420. DOI: 10.1038/cr.2011.22. View

2.
Londhe P, Zhu B, Abraham J, Keller C, Davie J . CIITA is silenced by epigenetic mechanisms that prevent the recruitment of transactivating factors in rhabdomyosarcoma cells. Int J Cancer. 2011; 131(4):E437-48. PMC: 3271171. DOI: 10.1002/ijc.26478. View

3.
Galanis E, Markovic S, Suman V, Nuovo G, Vile R, Kottke T . Phase II trial of intravenous administration of Reolysin(®) (Reovirus Serotype-3-dearing Strain) in patients with metastatic melanoma. Mol Ther. 2012; 20(10):1998-2003. PMC: 3464629. DOI: 10.1038/mt.2012.146. View

4.
Kanaseki T, Ikeda H, Takamura Y, Toyota M, Hirohashi Y, Tokino T . Histone deacetylation, but not hypermethylation, modifies class II transactivator and MHC class II gene expression in squamous cell carcinomas. J Immunol. 2003; 170(10):4980-5. DOI: 10.4049/jimmunol.170.10.4980. View

5.
Maldonado A, Klanke C, Jegga A, Aronow B, Mahller Y, Cripe T . Molecular engineering and validation of an oncolytic herpes simplex virus type 1 transcriptionally targeted to midkine-positive tumors. J Gene Med. 2010; 12(7):613-23. DOI: 10.1002/jgm.1479. View