Parity-Induced Protection Against Breast Cancer

Abstract

A woman's lifetime risk of developing breast cancer is significantly reduced by an early first full-term pregnancy. Thus, an early first childbirth is one of the most effective naturally occurring protective events that can diminish a woman's risk of breast cancer and is a candidate for targeted chemopreventive strategies. Although there is extensive epidemiological evidence in support of parity-induced protection against breast cancer, very little is known about the molecules and pathways responsible for this protective effect. Rodent carcinogenesis models mimic the epidemiology of early parity and provide a valuable system for examining the mechanism of parity-induced protection. As a means of addressing the molecular and cellular basis of parity-induced protection, we have conducted a broad-based gene expression analysis of nulliparous and parous murine mammary glands. As a result of this analysis, we have generated a panel of genes that molecularly define the protected parous mammary gland, including differentiation markers, immune-related genes, growth factors and TGF-Beta 3. To date, these findings represent the most comprehensive analysis of molecular differences induced in the mammary gland as a result of parity. Together, differential expression of distinct functional classes of molecules suggests novel mechanisms to explain parity-induced protection.

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Document Details

Document Type
Technical Report
Publication Date
Jul 01, 2001
Accession Number
ADB282185

Entities

People

  • Celina M. D'cruz

Organizations

  • University of Pennsylvania

Tags

DTIC Thesaurus Topics

  • B Lymphocytes
  • Birth
  • Breast Cancer
  • Carcinoma
  • Cell Line
  • Cell Physiological Processes
  • Cells
  • Dna Microarrays
  • Gene Expression
  • Genetics
  • Growth Factors
  • Lymphocytes
  • Microarray Analysis
  • Molecules
  • Neoplasms
  • Peptide Growth Factors
  • Peptides

Readers

  • Breast cancer cell signaling and growth regulation.
  • Molecular and genetic basis of cancer.
  • Women's Health and Cancer Risk Research: African American Women and Pregnancy Outcomes.

Technology Areas

  • Biotechnology