Cloning and Characterizing Genes Involved in Monoterpene Induced Mammary Tumor Regression.

Abstract

Monoterpene-induced/repressed genes were identified in regressing rat mammary carcinomas treated with dietary limonene using a newly developed method termed subtractive display. The subtractive display screen identified 42 monoterpene-induced genes comprising 9 known genes and 33 unidentified genes, as well as 58 monoterpene-repressed genes comprising 1 known gene and 57 unidentified genes. Several of the identified differentially expressed genes are involved in the mitoinhibitory transforming growth factor B signal tranduction pathway, as demonstrated by isolation of the mannose 6-phosphateAnsulin-like growth factor II receptor and the transforming growth factor B type II receptor. The monoterpene induced/repressed genes indicate that apoptosis and differentiation act in concert to effect carcinoma regression. Apoptosis is suggested by the cloning of a marker of programmed cell death, lipocortin 1. Consistent with a differentiation/remodeling process occurring during tumor regression, subtractive display identified YWK-II and neuroligin 1. Thus far, of the cDNAs putatively identified as differentially expressed in this complex in situ carcinoma model, 5 were tested, and each one has been confirmed to be differentially expressed. Additionally, many of the identified known genes are expressed as rare transcripts and exhibit small but significant changes in abundance.

Open PDF

Document Details

Document Type
Technical Report
Publication Date
Oct 01, 1996
Accession Number
ADA323218

Entities

People

  • Eric A. Ariazi
  • Michael N. Gould

Organizations

  • University of Wisconsin–Madison

Tags

DTIC Thesaurus Topics

  • Apoptosis
  • Body Weight
  • Breast Cancer
  • Cell Physiological Processes
  • Cells
  • Cellular Structures
  • Chemical Reactions
  • Chemical Synthesis
  • Chemistry
  • Chemotherapeutic Agents
  • Chemotherapy
  • Confocal Microscopy
  • Cytoskeleton
  • Genetic Structures
  • Phosphodiesterases
  • Programmed Cell Death
  • Tissues

Fields of Study

  • Biology

Readers

  • Molecular Biology and Genetics