The Role of AKT1 in Mammary Tumorigenesis and Transformation

Abstract

AKT1 belongs to the AKT/PKB protein-serine kinase family and is the cellular homolog of the v-akt oncogene. Gene amplification and overexpression of AKT are associated with adenocarcionomas of the stomach, breast, ovary, and pancreas. AKT1 is coupled to growth factor-dependent proliferation and resistance to apoptosis, but these processes have not been studied in either mammary epithelial cells or in breast cancer. The broad objectives of this proposal are to determine the role of the AKT1 in the proliferation, survival and transformation of mammary epithelial cells using two transgenic mouse strains in which expression of either AKT1 or a constitutively active form of AKT1 is directed to the mammary gland under the control of a mammary gland-specific promoter. The use of these two transgenic models will allow determination of the role of AKT1 in mammary gland hyperplasia, dysplasia and tumorigenesis, and will address the hypothesis that AKT1 is involved in the growth, survival, and transformation of mammary epithelial cells. This hypothesis will be tested using two experimental approaches. First, transgenic mice will be generated with mammary gland-directed expression of wild-type AKT1 or constitutively active myristoylated AKT1 (myrAKT1) to determine their effects on mammary hyperplasia and tumorigenesis. Second, primary mouse mammary epithelial cells will be transduced with ecotropic retroviruses expressing either AKT1 or myrAKT1 to determine their impact on growth factor-dependent proliferation, susceptibility to apoptosis induced by serum deprivation or the P13K inhibitor, LY294002, as well as transformation determined by anchorage-independent growth in soft agar and tumor formation in nude mice. Gene arrays of suppression subtractive hybridization will be used to identify genes modulated by AKT1 that are involved in its anti-apoptotic and proliferative activities.

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Document Details

Document Type
Technical Report
Publication Date
Sep 01, 2003
Accession Number
ADA418942

Entities

People

  • Robert I. Glazer

Organizations

  • Georgetown University

Tags

DTIC Thesaurus Topics

  • Biotechnology
  • Blood
  • Breast Cancer
  • Cell Line
  • Cell Physiological Processes
  • Cells
  • Cellular Structures
  • Chemistry
  • Epithelial Cells
  • Genetics
  • Growth Factors
  • Mammary Glands
  • Medical Personnel
  • Neoplasms
  • Peptide Growth Factors
  • Proteins
  • Stem Cells

Fields of Study

  • Biology

Readers

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