Interaction of viral oncoproteins with cellular target molecules: infection with high-risk vs low-risk human papillomaviruses

APMIS. 2010 Jun;118(6-7):471-93. doi: 10.1111/j.1600-0463.2010.02618.x.

Abstract

Persistent infection by a subgroup of so-called high-risk human papillomaviruses (HPVs) that have a tropism for mucosal epithelia has been defined as the cause of more than 98% of cervical carcinomas as well as a high proportion of other cancers of the anogenital region. Infection of squamous epithelial tissues in the head and neck region by these same high-risk HPVs is also associated with a subset of cancers. Despite the general conservation of genetic structure amongst all HPV types, infection by the low-risk types, whether in genital or head and neck sites, carries a negligible risk of malignant progression, and infections have a markedly different pathology. In this review, we will examine and discuss the interactions that the principal viral oncoproteins of the high-risk mucosotrophic HPVs and their counterparts from the low-risk group make with cellular target proteins, with a view to explaining the differences in their respective pathology.

Publication types

  • Review

MeSH terms

  • Animals
  • Cell Transformation, Neoplastic
  • Humans
  • Oncogene Proteins, Viral / physiology*
  • Papillomaviridae / pathogenicity*
  • Papillomavirus E7 Proteins / physiology*
  • Papillomavirus Infections / virology*
  • Repressor Proteins / physiology*
  • Retinoblastoma Protein / physiology
  • Telomerase / physiology
  • Tumor Suppressor Protein p53 / physiology

Substances

  • E6 protein, Human papillomavirus type 16
  • Oncogene Proteins, Viral
  • Papillomavirus E7 Proteins
  • Repressor Proteins
  • Retinoblastoma Protein
  • Tumor Suppressor Protein p53
  • oncogene protein E7, Human papillomavirus type 16
  • Telomerase