Defining the steps in a multistep mouse model for mammary carcinogenesis

H. E. Varmus, L. A. Godley, S. Roy, I. C.A. Taylor, L. Yuschenkoff, Y. P. Shi -, D. Pinkel, J. Gray, R. Pyle, C. M. Aldaz, A. Bradley, D. Medina, L. A. Donehower

Research output: Contribution to journalArticle

4 Scopus citations

Abstract

The Wnt-1 transgenic system has provided a rich model for studying mammary tumorigenesis in the mouse. Crossing these animals to other transgenic animals and infecting them with MMTV have forcefully demonstrated the synergy between Wnt-1 and members of the Fgf family. Mammary tumors from Wnt-1 TG/p53-deficient mice present novel features: a less fibrotic histology, rapid kinetics of tumor formation, and increased genomic instability. Understanding the molecular basis for such phenotypes may provide insights into the behavior of human tumors, especially those in which p53 has been affected.

Original languageEnglish (US)
Pages (from-to)491-499
Number of pages9
JournalCold Spring Harbor symposia on quantitative biology
Volume59
DOIs
StatePublished - 1994

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Biology
  • Genetics

Fingerprint Dive into the research topics of 'Defining the steps in a multistep mouse model for mammary carcinogenesis'. Together they form a unique fingerprint.

  • Cite this

    Varmus, H. E., Godley, L. A., Roy, S., Taylor, I. C. A., Yuschenkoff, L., Shi -, Y. P., Pinkel, D., Gray, J., Pyle, R., Aldaz, C. M., Bradley, A., Medina, D., & Donehower, L. A. (1994). Defining the steps in a multistep mouse model for mammary carcinogenesis. Cold Spring Harbor symposia on quantitative biology, 59, 491-499. https://doi.org/10.1101/SQB.1994.059.01.054