The absence of fundamental knowledge of the genitourinary tract severely limits the development of new and innovative therapeutic options for a variety of common illnesses, including age-related and post-partum urinary incontinence, various forms of bladder instability, urinary tract complications of benign prostatic disease, chronic pelvic pain, and voiding dysfunction originating from congenital anomalies. In the following pages we describe our vision for a research center of excellence in urology, which we have named the Harvard Urologic Research Center (HURC). Our major goal in developing this program has been to assemble an interdisciplinary team of investigators who employ state-of-the-art approaches in basic science and translational research, who have had a history of highly successful collaborative relationships, and who are committed to working together to bring a broad range of technical and scientific expertise to fundamental studies of urological disease. The integrative theme of the HURC is """"""""Tissue Renewal in the Genitourinary Tract"""""""". Implicit in this theme is the recognition that many functional deficits observed clinically in urologic practice might be reversed or restored if sufficient knowledge about tissue architecture and remodeling, intercellular circuitry and cell signaling, and other processes characteristic of the cells and tissues of the urogenital system were understood in fundamental terms. The long-range objective of this program will be to integrate knowledge in basic cell biology, tissue engineering, biochemistry, molecular biology, proteomics, and genomics into a scientific network of collaboration that has not existed before. The four """"""""missions"""""""" of the HURC will be to: (1) significantly expand the fundamental knowledge of the hollow organs of the urinary tract (ureter, bladder and urethra); (2) direct new, cutting-edge technologies specifically toward clinical urological problems, including cancer; (3) create a center of research and teaching excellence that will attract investigators nationally and internationally; and (4) establish a mentoring environment that will encourage outstanding new investigators to focus on urologic diseases in their career path. To support the """"""""Tissue Renewal"""""""" theme, the investigators in the HURC will be clustered within three primary areas of scientific focus that will serve as anchor disciplines for the Center: (1) Tissue Engineering, (2) Signal Transduction and (3) Angiogenesis/Vascular Biology. We seek to create a totally new program in urology research, one that has the potential to develop into one of the strongest and most innovative investigative programs focused on urologic disease in the world.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Specialized Center (P50)
Project #
5P50DK065298-04
Application #
7122148
Study Section
Special Emphasis Panel (ZDK1-GRB-9 (M1))
Program Officer
Hoshizaki, Deborah K
Project Start
2003-09-15
Project End
2008-08-31
Budget Start
2006-09-01
Budget End
2007-08-31
Support Year
4
Fiscal Year
2006
Total Cost
$1,108,206
Indirect Cost
Name
Children's Hospital Boston
Department
Type
DUNS #
076593722
City
Boston
State
MA
Country
United States
Zip Code
02115
Vasquez, Evalynn; Cristofaro, Vivian; Lukianov, Stefan et al. (2017) Deletion of neuropilin 2 enhances detrusor contractility following bladder outlet obstruction. JCI Insight 2:e90617
Doyle, Claire; Cristofaro, Vivian; Sack, Bryan S et al. (2017) Inosine attenuates spontaneous activity in the rat neurogenic bladder through an A2B pathway. Sci Rep 7:44416
Mucka, Patrick; Levonyak, Nicholas; Geretti, Elena et al. (2016) Inflammation and Lymphedema Are Exacerbated and Prolonged by Neuropilin 2 Deficiency. Am J Pathol 186:2803-2812
De Filippo, Roger E; Kornitzer, Benjamin S; Yoo, James J et al. (2015) Penile urethra replacement with autologous cell-seeded tubularized collagen matrices. J Tissue Eng Regen Med 9:257-64
Mauney, Joshua R; Adam, Rosalyn M (2015) Dynamic reciprocity in cell-scaffold interactions. Adv Drug Deliv Rev 82-83:77-85
Chung, Yeun Goo; Seth, Abhishek; Doyle, Claire et al. (2015) Inosine Improves Neurogenic Detrusor Overactivity following Spinal Cord Injury. PLoS One 10:e0141492
Sun, Y; Kaneko, S; Li, X K et al. (2015) The PI3K/Akt signal hyperactivates Eya1 via the SUMOylation pathway. Oncogene 34:2527-37
Morley, Samantha; You, Sungyong; Pollan, Sara et al. (2015) Regulation of microtubule dynamics by DIAPH3 influences amoeboid tumor cell mechanics and sensitivity to taxanes. Sci Rep 5:12136
Kanellis, D C; Bursac, S; Tsichlis, P N et al. (2015) Physical and functional interaction of the TPL2 kinase with nucleophosmin. Oncogene 34:2516-26
Yang, Wei; Ramachandran, Aruna; You, Sungyong et al. (2014) Integration of proteomic and transcriptomic profiles identifies a novel PDGF-MYC network in human smooth muscle cells. Cell Commun Signal 12:44

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