The three research projects that comprise this Program Project are all focused on understanding molecular and cellular events and mechanisms leading to bladder tumorigenesis of both major bladder cancer (BC) variants and molecular subtypes. In addition to the intellectual and experimental synergies that link the individual projects into a cohesive program, each of the three proposed research plans all depend upon a common set of critical reagents and services made available on a continuous basis for their success. These include but are not limited to a set of cultured cell lines that represent different grades and stages of major BC variants and molecular subtypes, unique mouse models of bladder cancer developed/used by project leaders Dr. Wu, Dr. Tang and Dr. Huang, nucleic acid reagents, antibodies and cDNA constructs. Obviously, it would not make sense, nor would it be an efficient use of time, money, and resources for each laboratory to independently generate, procure, characterize, and maintain all these reagents. Instead, we have established a centralized Reagent and Service Core, one of whose purposes is to serve as a central repository for key reagents and provide a central supply for these important research tools that can be shared by all involved in this Program Project. In addition to the cost-effectiveness, this approach offers the advantage of ensuring the quality of these shared reagents across the individual projects. Providing supplies of cell lines, mouse tissues and animal models from a centralized core eliminates variability in reagent handling, facilitating data comparison amongst the three individual projects. Furthermore, it promotes additional interactions among the project directors and guards against accidental loss of invaluable reagents in emergency situations such as power outages (which we last experienced in 2012 during Sandy Superstorm). Finally, the Core B will also provide pathology and statistical support for the individual projects.
The specific aims of the Core are: i) To maintain a centralized supply and distribute a common core set of reagents vital to support the research efforts of individual component projects; ii) To collect mouse specimens and provide the necessary pathology support service; and iii) To provide dedicated statistical support. Success of this Core will be an essential factor for the studies that have been proposed in this program project.

Public Health Relevance

This Program Project seeks to understand the mechanisms involved in bladder tumorigenesis leading to different types of bladder cancer. The three projects will use a common set of reagents and services. The Core bundles these critical reagents and services together and serves as a central clearinghouse, ensuring their timely, cost-effective distribution, which will directly facilitate the success of this Program Project. OMB No. 0925-0001/0002 (Rev. 03/16 Approved Through 10/31/2018) Page Continuation Format Page

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
5P01CA165980-07
Application #
9994206
Study Section
Special Emphasis Panel (ZCA1)
Project Start
2013-09-12
Project End
2024-08-31
Budget Start
2020-09-01
Budget End
2021-08-31
Support Year
7
Fiscal Year
2020
Total Cost
Indirect Cost
Name
New York University
Department
Type
DUNS #
121911077
City
New York
State
NY
Country
United States
Zip Code
10016
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Weng, Mao-Wen; Lee, Hyun-Wook; Choi, Bongkun et al. (2017) AFB1 hepatocarcinogenesis is via lipid peroxidation that inhibits DNA repair, sensitizes mutation susceptibility and induces aldehyde-DNA adducts at p53 mutational hotspot codon 249. Oncotarget 8:18213-18226
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