Overall goals of the proposed work: The human prostate gland is enlarged with age. The molecular mechanisms that lead to this age-related re-growth of the prostate are essentially unknown. The objective of the proposed research is to study the mechanism underlying initiation of the age-related re-growth of the prostate. We found that the protein (WDR77) in the cytoplasm is essential and sufficient to drive growth of prostate cells at the early stage of prostate development. The WDR77-driven cell growth is ceased in adult prostate but the WDR77-driven cell growth is re-activated during prostate aging process. As the consequence of this event, the age-related cell growth is initiated.
Aim 1 will study how the WDR77 gene is re-activated in stromal cells in the aging prostate. The proposed research in Aims 2 and 3 will investigate the molecular mechanisms by which WDR77 promotes cellular proliferation. Significance of the proposed research: Our studies identify a novel mechanism by which WDR77 contributes to the age-related prostate growth. The proposed research will investigate how WDR77 is re-activated in aging prostate and the mechanisms by which WDR77 drives cell growth. This study represents a novel study concept that relates to the basic biology of prostate aging. The study will not only help to understand the basic biology of prostate aging and provide a novel strategy but also prevent the development of various prostatic diseases by specifically inhibiting the age-relate re-growth of the prostate in old men. Thus, the proposed research fits to the NIA's mission -- To help improve the health and well-being of old people through research.

Public Health Relevance

The study will help to understand the basic biology of prostate aging and provide a novel strategy to prevent the development of various prostatic diseases by specifically inhibiting the age-relate re-growth of the prostate in old men.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Academic Research Enhancement Awards (AREA) (R15)
Project #
1R15AG056867-01A1
Application #
9514566
Study Section
Nuclear and Cytoplasmic Structure/Function and Dynamics Study Section (NCSD)
Program Officer
Kerr, Candace L
Project Start
2018-09-01
Project End
2021-08-31
Budget Start
2018-09-01
Budget End
2021-08-31
Support Year
1
Fiscal Year
2018
Total Cost
Indirect Cost
Name
Clark Atlanta University
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
065325177
City
Atlanta
State
GA
Country
United States
Zip Code
30314