Under certain conditions progestins have been shown to stimulate the growth of the human breast cancer cell line, T-47D. The overall aim of this proposal is to determine the mechanisms of progestin induced growth stimulation. Preliminary studies from this laboratory have indicated that under the above conditions, progestins increase the level of c-myc mRNA. The current proposal aims to understand how progestins do this.
Four specific aims are listed:1. To determine if the increase in c-myc mRNA is a primary response to progestins i.e is it independent of protein synthesis. 2. To determine if a functional progestin response element is present in the c-myc gene.3. To address the question: Is enhanced c-myc expression necessary for progestin induced proliferation? 4. To address the question: Why is c-myc responsive to progestins in T-47D cells but not in MCF-7 cells, which are both progesterone receptor positive?

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA055665-03
Application #
2096780
Study Section
Reproductive Endocrinology Study Section (REN)
Project Start
1992-04-23
Project End
1996-03-31
Budget Start
1994-04-01
Budget End
1996-03-31
Support Year
3
Fiscal Year
1994
Total Cost
Indirect Cost
Name
Marshall University
Department
Biochemistry
Type
Schools of Medicine
DUNS #
036156615
City
Huntington
State
WV
Country
United States
Zip Code
25701
Moore, M R; Zhou, J L; Blankenship, K A et al. (1997) A sequence in the 5' flanking region confers progestin responsiveness on the human c-myc gene. J Steroid Biochem Mol Biol 62:243-52