The West Virginia University Flow Cytometry Core was established in 2001 as part of the Phase 1 Center for Biomedical Research Excellence (CoBRE) grant in Signal Transduction and Cancer submitted by the Mary Babb Randolph Cancer Center (MBRCC). The Flow Cytometry Core offers analytic flow cytometry and cell sorting to WVU and neighboring institutions, and supports CoBRE investigators as well as other NIH-funded projects. This application describes 1) the Core's past contribution to research at WVU, 2) selected specific scientific projects in cancer research that are NIH funded and dependent on the Flow Cytometry Core, 3) core personnel, and 4) the Core's operational plan. As a consistent goal within the CoBRE grants at all Phases (1-111) the Core will continue efforts to contribute to training and mentoring of investigators that utilize this resource. This will occur, in part, through participation in the Technology Seminar Series which is overseen by the Administrative Core. This seminar series provides the opportunity for MBRCC investigators, as well as other scientists who utilize the core, to be exposed to Flow Cytometry-based technologies that may augment their research. The Director of the Core will continue to attend classes and workshops for training in new technologies that will continue to support this Core as a dynamic resource that is responsive to changing research trends and investigator needs. The Facility will continue to play an integral role in current and future cancer-related projects including research projects designed to translate novel and innovative therapies to cancer patients in West Virginia. Finally, a strategy to ensure sustainability of the Flow Cytometry Core beyond Phase 111 of the CoBRE program is described in the following section as an essential consideration to the long-term growth of the MBRCC and our capacity to continue to provide optimal access to appropriate technology.

Public Health Relevance

The Flow Cytometry Core is an integral component of the CoBRE in Signal Transduction and Cancer. The CoBRE supports biomedical research in cancer at WVU, which has the goal of improving patient health by understanding mechanisms of cancer cell signaling, and translating that information to developing new therapies for cancer.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Center Core Grants (P30)
Project #
3P30GM103488-05S1
Application #
9335551
Study Section
Special Emphasis Panel (ZRR1-RI-B (01))
Program Officer
Zlotnik, Hinda
Project Start
Project End
2018-06-30
Budget Start
2015-07-01
Budget End
2017-06-30
Support Year
5
Fiscal Year
2016
Total Cost
$386,688
Indirect Cost
$127,563
Name
West Virginia University
Department
Type
DUNS #
191510239
City
Morgantown
State
WV
Country
United States
Zip Code
26506
Bland, Cassidy L; Byrne-Hoffman, Christina N; Fernandez, Audry et al. (2018) Exosomes derived from B16F0 melanoma cells alter the transcriptome of cytotoxic T cells that impacts mitochondrial respiration. FEBS J 285:1033-1050
Mohammad, Afroz S; Griffith, Jessica I; Adkins, Chris E et al. (2018) Liposomal Irinotecan Accumulates in Metastatic Lesions, Crosses the Blood-Tumor Barrier (BTB), and Prolongs Survival in an Experimental Model of Brain Metastases of Triple Negative Breast Cancer. Pharm Res 35:31
Zhang, Shichao; Xing, Malcolm M Q; Li, Bingyun (2018) Capsule Integrated Polypeptide Multilayer Films for Effective pH-Responsive Multiple Drug Co-Delivery. ACS Appl Mater Interfaces :
Shepherd, Danielle L; Hathaway, Quincy A; Nichols, Cody E et al. (2018) Mitochondrial proteome disruption in the diabetic heart through targeted epigenetic regulation at the mitochondrial heat shock protein 70 (mtHsp70) nuclear locus. J Mol Cell Cardiol 119:104-115
Grisez, Brian T; Ray, Justin J; Bostian, Phillip A et al. (2018) Highly metastatic K7M2 cell line: A novel murine model capable of in vivo imaging via luciferase vector transfection. J Orthop Res :
Boehm, Dylan T; Hall, Jesse M; Wong, Ting Y et al. (2018) Evaluation of Adenylate Cyclase Toxoid Antigen in Acellular Pertussis Vaccines by Using a Bordetella pertussis Challenge Model in Mice. Infect Immun 86:
Nichols, Cody E; Shepherd, Danielle L; Hathaway, Quincy A et al. (2018) Reactive oxygen species damage drives cardiac and mitochondrial dysfunction following acute nano-titanium dioxide inhalation exposure. Nanotoxicology 12:32-48
McNitt, Dudley H; Choi, Soo Jeon; Keene, Douglas R et al. (2018) Surface-exposed loops and an acidic patch in the Scl1 protein of group A Streptococcus enable Scl1 binding to wound-associated fibronectin. J Biol Chem 293:7796-7810
Shumar, Stephanie A; Kerr, Evan W; Geldenhuys, Werner J et al. (2018) Nudt19 is a renal CoA diphosphohydrolase with biochemical and regulatory properties that are distinct from the hepatic Nudt7 isoform. J Biol Chem 293:4134-4148
Famodu, Oluremi A; Barr, Makenzie L; Colby, Sarah E et al. (2018) Neck Circumference Positively Relates to Cardiovascular Risk Factors in College Students. Int J Environ Res Public Health 15:

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