C-KIT AND Stem Cell Factor Expression in Breast Cancer

Abstract

We have proceeded to investigate some of the biologic consequences of c-kit and SCF coexpression since simple coexpression of receptor and ligand may imply, but does not prove, a potential autocrine(or paracrine) loop. We have therefore, constructed an autocrine loop by transfecting the breast cancer cell line, MCF7, that only expresses SCF, with a c-kit expression vector (21). MCF7 cells were transfected with both the c-kit expression vector and the empty pCEP4 vector (to serve as a control). Since the vector contained a hygromycin resistance gene, stable transfectants could be selected based on their survival in hygromycin-containing media.

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Document Details

Document Type
Technical Report
Publication Date
Sep 01, 1997
Accession Number
ADA335102

Entities

People

  • Susan Hines

Organizations

  • Virginia Commonwealth University

Tags

DTIC Thesaurus Topics

  • Additives (Chemicals)
  • Albumins
  • Amino Acids
  • Blood
  • Breast Cancer
  • Cell Line
  • Cell Physiological Processes
  • Cells
  • Chemistry
  • Growth Factors
  • Mammary Glands
  • Neoplasms
  • Peptide Growth Factors
  • Peptides
  • Proteins
  • Stem Cells
  • Tyrosine

Fields of Study

  • Biology

Readers

  • Molecular Genetics
  • Oncology (Cancer Research).
  • Quantum Chemistry

Technology Areas

  • Biotechnology
  • Biotechnology - Cancer Biotech