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Microarray-based Identification of Individual HERV Loci Expression: Application to Biomarker Discovery in Prostate Cancer
Published on: November 2, 2013
Retroviruses and the genetics of cancer
1McArdle Laboratory, University of Wisconsin, Madison 53706.
Abstract:
Retroviruses cause cancer by several different mechanisms including addition of an oncogene, addition of a modified viral glycoprotein, activation of a proto-oncogene, transactivation of a proto-oncogene, immune depression, and stimulation of lymphoid cell proliferation. Both the evolution of oncogenes and tumor induction by most retroviruses is multi-step. Study of the evolution of a particular oncogene, v-rel, indicates that this evolution could not have been selection-driven, but that it resulted from the high rate of mutation in retroviruses replication, that is, it was mutation-driven. Argument is made that much other cancer is also mutation-driven.
Insights
Retroviruses can cause cancer through various mechanisms, often involving multiple steps. The evolution of oncogenes, like v-rel, appears mutation-driven rather than selection-driven, suggesting mutations play a key role in cancer development.
Area of Science:
- Oncology
- Virology
- Molecular Biology
Background:
- Retroviruses are known etiological agents in cancer development.
- Cancer induction by retroviruses involves multiple mechanisms and steps.
- Oncogene evolution is a critical factor in tumorigenesis.
Purpose of the Study:
- To elucidate the mechanisms by which retroviruses induce cancer.
- To investigate the evolutionary drivers of oncogene development.
- To propose a mutation-driven model for cancer evolution.
Main Methods:
- Review of retroviral oncogenesis mechanisms.
- Analysis of oncogene evolution, specifically v-rel.
- Comparative analysis of selection-driven versus mutation-driven evolutionary models.
Main Results:
- Retroviral cancer mechanisms include oncogene addition, proto-oncogene activation, immune suppression, and lymphoid proliferation.
- The evolution of the v-rel oncogene is demonstrated to be mutation-driven, not selection-driven.
- Retroviral replication's high mutation rate is implicated in oncogene evolution.
Conclusions:
- Retroviral oncogenesis is a multi-step process involving diverse mechanisms.
- Oncogene evolution, exemplified by v-rel, is primarily driven by high mutation rates in retroviruses.
- A significant portion of other cancers may also be mutation-driven.
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