Literature DB >> 35143960

Histone modifiers at the crossroads of oncolytic and oncogenic viruses.

Sara A Murphy1, Norman John Mapes2, Devika Dua3, Balveen Kaur4.   

Abstract

Cancer is a disease caused by loss of regulatory processes that control the cell cycle, resulting in increased proliferation. The loss of control can deregulate both tumor suppressors and oncogenes. Apart from cell intrinsic gene mutations and environmental factors, infection by cancer-causing viruses also induces changes that lead to malignant transformation. This can be caused by both expression of oncogenic viral proteins and also by changes in cellular genes and proteins that affect the epigenome. Thus, these epigenetic modifiers are good therapeutic targets, and several epigenetic inhibitors are approved for the treatment of different cancers. In addition to small molecule drugs, biological therapies, such as antibodies and viral therapies, are also increasingly being used to treat cancer. An HSV-1-derived oncolytic virus is currently approved by the US FDA and the European Medicines Agency. Similarly, an adenovirus-based therapeutic is approved for use in China for some cancer types. Because viruses can affect cellular epigenetics, the interaction of epigenome-targeting drugs with oncogenic and oncolytic viruses is a highly significant area of investigation. Here, we will review the current knowledge about the impact of using epigenetic drugs in tumors positive for oncogenic viruses or as therapeutic combinations with oncolytic viruses.
Copyright © 2022. Published by Elsevier Inc.

Entities:  

Keywords:  DNA; acetylation; cancer; epigenetic modifiers; gene therapy; histone; methylation; oncolytic virus; viruses

Mesh:

Substances:

Year:  2022        PMID: 35143960      PMCID: PMC9171252          DOI: 10.1016/j.ymthe.2022.02.006

Source DB:  PubMed          Journal:  Mol Ther        ISSN: 1525-0016            Impact factor:   12.910


  100 in total

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Review 4.  Acetylation of proteins as novel target for antitumor therapy: review article.

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8.  Vorinostat-An Overview.

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Journal:  Indian J Dermatol       Date:  2015 Jul-Aug       Impact factor: 1.494

9.  KSHV encoded ORF59 modulates histone arginine methylation of the viral genome to promote viral reactivation.

Authors:  Roxanne C Strahan; Maria McDowell-Sargent; Timsy Uppal; Pravinkumar Purushothaman; Subhash C Verma
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10.  Combining protein arginine methyltransferase inhibitor and anti-programmed death-ligand-1 inhibits pancreatic cancer progression.

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  1 in total

Review 1.  Improving cancer immunotherapy by rationally combining oncolytic virus with modulators targeting key signaling pathways.

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  1 in total

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