The COBRE Center for Cancer Research Development (CCRD) has become an integral part of the resources and environment of the cancer research infrastructure at RIH. Our Phase I and II periods were characterized by outstanding junior investigator productivity in terms of peer reviewed publications (n=145) and success in obtaining extramural, federal funding ($23,265,020.) The original scientific theme of the Phase I and Phase II awards was to emphasize research on mechanisms of cancer and its origins. This focus on cancer biology will be maintained through the Phase III COBRE by continuing to stimulate awards and core user credits to junior investigators interested in cancer through a new Pilot Grants Core. During the past five years RIH has made a substantial institutional investment in clinical and basic research in cancer. This increase in investigation has had a positive effect on the CCRD Core facilities as it has created an increased local customer base. This expanded customer base will be factored into a strategic plan for sustaining the CCRD core facilities beyond the Phase III period with strong institutional funding. The following four aims are proposed:
(Aim 1) To continue to enhance the ability of the Administrative Core to oversee the goals of the COBRE CCRD through maturing of the Molecular Pathology and Proteomics Cores with less reliance on NIH support during Phase III.
(Aim 2) To continue to keep the Proteomics Core facility at the cutting edge of rapidly evolving mass spectroscopic technologies associated with global proteomics and identification of candidate proteins in isolation or within tissues.
(Aim 3) To provide molecular pathology services including archived tumor bank specimens for enhancing productivity and research capabilities of investigators at all levels of expertise in order to address research problems and to increase their competitiveness for extramural funding.
(Aim 4) To provide pilot grants and core user credits to solely support junior investigators interested in cancer research and to offer bioinformatic analysis to recipients of pilot awards.

Public Health Relevance

The COBRE CCRD provides state-of-the-art core services in Proteomics and Molecular Pathology to biomedical investigators pursuing cancer research. The program also supports junior faculty with mentoring activities and financial support.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Center Core Grants (P30)
Project #
5P30GM110759-03
Application #
9266449
Study Section
Special Emphasis Panel (ZGM1)
Program Officer
Gao, Hongwei
Project Start
2015-05-01
Project End
2020-04-30
Budget Start
2017-05-01
Budget End
2018-04-30
Support Year
3
Fiscal Year
2017
Total Cost
Indirect Cost
Name
Rhode Island Hospital
Department
Type
DUNS #
075710996
City
Providence
State
RI
Country
United States
Zip Code
02903
Patel, Mohak; Leggett, Susan E; Landauer, Alexander K et al. (2018) Rapid, topology-based particle tracking for high-resolution measurements of large complex 3D motion fields. Sci Rep 8:5581
Lo, Wan-Lin; Shah, Neel H; Ahsan, Nagib et al. (2018) Lck promotes Zap70-dependent LAT phosphorylation by bridging Zap70 to LAT. Nat Immunol 19:733-741
Chorzalska, Anna; Ahsan, Nagib; Rao, R Shyama Prasad et al. (2018) Overexpression of Tpl2 is linked to imatinib resistance and activation of MEK-ERK and NF-?B pathways in a model of chronic myeloid leukemia. Mol Oncol 12:630-647
Valentin, Thomas M; Leggett, Susan E; Chen, Po-Yen et al. (2017) Stereolithographic printing of ionically-crosslinked alginate hydrogels for degradable biomaterials and microfluidics. Lab Chip 17:3474-3488
Ahsan, Nagib; Belmont, Judson; Chen, Zhuo et al. (2017) Highly reproducible improved label-free quantitative analysis of cellular phosphoproteome by optimization of LC-MS/MS gradient and analytical column construction. J Proteomics 165:69-74
Chorzalska, Anna; Kim, Javier Flores; Roder, Karim et al. (2017) Long-Term Exposure to Imatinib Mesylate Downregulates Hippo Pathway and Activates YAP in a Model of Chronic Myelogenous Leukemia. Stem Cells Dev 26:656-677
Ahsan, Nagib; Salomon, Arthur R (2017) Quantitative Phosphoproteomic Analysis of T-Cell Receptor Signaling. Methods Mol Biol 1584:369-382
Zhao, Chaohui Lisa; Hui, Yiang; Wang, Li Juan et al. (2017) T-complex-associated-testis-expressed 3 (TCTE3) is a novel marker for pancreatobiliary carcinomas. Hum Pathol 70:62-69
Belmont, Judson; Gu, Tao; Mudd, Ashley et al. (2017) A PLC-?1 Feedback Pathway Regulates Lck Substrate Phosphorylation at the T-Cell Receptor and SLP-76 Complex. J Proteome Res 16:2729-2742
Punsoni, Michael; Mangray, Shamlal; Lombardo, Kara A et al. (2017) Succinate Dehydrogenase B (SDHB) Immunohistochemistry for the Evaluation of Muscle Biopsies. Appl Immunohistochem Mol Morphol 25:645-650

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