The Role of Amplified Wild-Type Neu in the Etiology of Breast Cancer

Abstract

Many human breast cancers have amplified wild-type Neu (Her2) protooncogenes. It is still not known from either human or rodent models if amplified wild-type Neu is involved in the etiology of breast cancer, We have begun to develop rat transgenic models. Under the first aim we will construct additional Neu transgenic rat lines. Aim 2 will endocrinologically manipulate female Neu-transgenic rats in a way that models high androgen postmenopausal women. Aim 3 will explore alternative reasons of why these female transgenics do not develop breast cancer. The role of genetic background as it relates to female breast cancer development in this model will be explored. We have produced two independent strains of Neu-transgenic rats that spontaneously develop mammary carcinomas in males. Females supplemented with androgens develop mammary carcinomas. These carcinomas activated Neu by amplification and not by mutagenesis. We have thus developed a useful model of Neu associated mammary carcinogenesis. This answers a key question of whether the amplification of wild-type Neu is only associated with tumor progression or is it also possibly involved in breast cancer etiology. These data presented is the first model to clearly demonstrate that the amplification of wild type Neu can induce mammary cancer. In addition we also show that the genetic penetrance of neu can be altered by different modifier genes on varying genetic backgrounds. This suggests that these modifiers may be good biomarker or drug targets for neu associated breast cancer.

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Document Details

Document Type
Technical Report
Publication Date
Jul 01, 2004
Accession Number
ADA429151

Entities

People

  • Michael N. Gould

Organizations

  • University of Wisconsin–Madison

Tags

DTIC Thesaurus Topics

  • Androgen Receptors
  • Biomedical Research
  • Blood
  • Breast Cancer
  • Cells
  • Chemical Synthesis
  • Chemistry
  • Epithelial Cells
  • Genetically Modified Organisms
  • Genetics
  • Mammary Glands
  • Medical Personnel
  • Neoplasms
  • Oncology
  • Prostate Cancer
  • Sex Glands
  • Tissues

Fields of Study

  • Biology

Readers

  • Breast cancer cell signaling and growth regulation.
  • Molecular Biology and Genetics
  • Molecular and genetic basis of cancer.

Technology Areas

  • Biotechnology