Changes in frequency, morphology, and behavior of tumors induced in mice by a polyoma virus mutant with a specifically altered oncogene

Am J Pathol. 1992 Dec;141(6):1409-25.

Abstract

Alterations in the tumor-inducing ability of a polyoma virus mutant encoding a partially defective middle T oncogene have been investigated. The mutant middle T associates with and activates the tyrosine protein kinase pp60c-src normally but does not promote binding of a second enzyme, phosphatidyl-inositol 3-kinase. Compared with the wild type virus, this mutant shows an altered and reduced ability to induce tumors after inoculation into newborn mice, as judged by the following criteria: lower frequency of tumors, reduced morbidity and increased survival times of host mice, changes in the spectrum of tumor types, and altered morphologic properties of tumors at several target organ sites. These results indicate an important role of changes in 3-phosphoinositide metabolism in induction of a variety of tumors in this experimental system.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Enzyme Activation
  • Female
  • Immunohistochemistry
  • In Situ Hybridization
  • Incidence
  • Male
  • Mammary Neoplasms, Experimental / epidemiology*
  • Mammary Neoplasms, Experimental / etiology*
  • Mammary Neoplasms, Experimental / pathology*
  • Mice
  • Mice, Inbred C3H
  • Mutation / genetics*
  • Oncogenes / genetics*
  • Oncogenes / physiology
  • Phosphatidylinositols / metabolism
  • Polyomavirus / genetics*
  • Polyomavirus / physiology*
  • Protein-Tyrosine Kinases / metabolism
  • Protein-Tyrosine Kinases / physiology
  • Salivary Gland Neoplasms / epidemiology
  • Salivary Gland Neoplasms / etiology
  • Salivary Gland Neoplasms / pathology
  • Sex Factors
  • Skin Neoplasms / epidemiology*
  • Skin Neoplasms / etiology*
  • Skin Neoplasms / pathology
  • Thymus Neoplasms / epidemiology
  • Thymus Neoplasms / etiology
  • Thymus Neoplasms / pathology
  • Virus Replication

Substances

  • Phosphatidylinositols
  • Protein-Tyrosine Kinases