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Published on: April 3, 2018
Exploring the Isoprenoid Biosynthesis Pathway's Role in Oncogenic Viruses
Louise N Blaha1,2, Jeffrey D Neighbors1,2, Richa Sandeep3
1Penn State Cancer Institute, Hershey, PA 17033, USA.
Abstract:
Oncogenic viruses, which are causative for some cancers, are typically acquired in youth and suppressed until older age. These malignancies account for over 10% of the cancer burden and often reprogram cellular metabolic pathways to promote their own survival and proliferation, often targeting lipogenic pathways to increase bioavailability of cellular products. The isoprenoid biosynthesis pathway (IBP) is an important lipogenic pathway that has been explored extensively for its dysregulation contributing to carcinogenesis, with notable discussion of statin therapy as a means of perturbing neoplasia. To our knowledge, we are the first group to provide a comprehensive discussion of the seven known oncogenic viruses and their reliance upon the IBP to promote tumorigenesis. As knowledge on this topic is limited, we aim to draw attention to a neglected area of the oncogenic research space, while also highlighting the use of inhibitors of the IBP as potential avenues for novel treatment options.
Insights
Oncogenic viruses drive over 10% of cancers by reprogramming cellular metabolism, particularly the isoprenoid biosynthesis pathway (IBP). This study highlights the IBP
Area of Science:
- Oncology
- Virology
- Metabolic Pathways
Background:
- Oncogenic viruses cause over 10% of human cancers.
- These viruses often reprogram host cellular metabolism for survival and proliferation.
- Lipogenic pathways, including the isoprenoid biosynthesis pathway (IBP), are frequently targeted.
Purpose of the Study:
- To comprehensively discuss the seven known oncogenic viruses and their dependence on the IBP for tumorigenesis.
- To highlight a neglected area in oncogenic research.
- To explore inhibitors of the IBP as potential novel cancer therapies.
Main Methods:
- Comprehensive literature review and discussion.
- Analysis of the role of the isoprenoid biosynthesis pathway (IBP) in virus-associated cancers.
- Exploration of existing and potential therapeutic strategies targeting the IBP.
Main Results:
- Oncogenic viruses rely on the isoprenoid biosynthesis pathway (IBP) for promoting tumor development.
- Dysregulation of the IBP is a common mechanism in virus-induced carcinogenesis.
- Inhibitors of the IBP represent a promising therapeutic avenue.
Conclusions:
- The isoprenoid biosynthesis pathway (IBP) is a critical factor in oncogenesis driven by viruses.
- Targeting the IBP offers a novel strategy for treating virus-associated cancers.
- Further research into IBP inhibitors is warranted for cancer therapy development.
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