Is the Regenerative Capacity of the Mammary Gland Contained With Those Mammary Cells That Express the Progesterone Receptor? Implications for Breast Cancer

Abstract

We hypothesized that mammary-specific stem cells are present as a subgroup within those epithelial cells that express the progesterone receptor (PR) . To determine whether a stem cell population is contained within the PR expressing cell population (PR+), a recently generated (yet to be published) PR-lacZ knockin mouse in combination with fluorescent- activated cell sorting (PACS) was utilized to separate PR+ from PR- mammary cells; both cell populations would then be evaluated for their regenerative capacity by transplantation into the cleared mammary fat pad of a host animal. As previously described in our final report, PACS analysis applied to the PR-lacZ mammary gland provided a significantly enriched (^70%) PR+ mammary epithelial cell population that maintained lacz expression in culture. Although, PR+ and PR- enriched mammary epithelial cell populations were transplanted into mammary fat pads, these host animals as well as much of the PR-lacZ colony were lost to Tropical Storm "Allison". To estimate the regenerative potential of the above mammary epithelial cell population, a 6-month no cost extension was requested. Unfortunately, due to severity of the loss of the PR-lacz mouse colony, this extension was not sufficient to allow recovery and rederivation of the PR-lacz colony.

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Document Details

Document Type
Technical Report
Publication Date
Mar 01, 2002
Accession Number
ADA405242

Entities

People

  • John P. Lydon

Organizations

  • Baylor College of Medicine

Tags

DTIC Thesaurus Topics

  • Abstracts
  • Biomedical Research
  • Breast Cancer
  • Cells
  • Classification
  • Electronic Mail
  • Glands
  • Information Operations
  • Mammary Glands
  • Maryland
  • Monitoring
  • Neoplasms
  • Progesterone
  • Security
  • Stem Cells

Fields of Study

  • Biology

Readers

  • Atmospheric Remote Sensing.
  • Breast cancer cell signaling and growth regulation.
  • Oncology (Cancer Research).

Technology Areas

  • Biotechnology