The Cellular Immunology and Immune Metabolism Core (CIMC) of the LSU-Cancer Center was created in 2006 with the objective of providing flow cytometry support to Promising Junior Investigators (PJI) funded during Phase I of the COBRE ?Mentoring Translational Researchers in Louisiana?. During Phase II, and under the scientific direction of Dr. Paulo Rodriguez, and with the oversight of Dr. Augusto Ochoa, the CIMC evolved to provide cutting edge technologies not only to COBRE-supported PJI, but also to the LSUHSC investigators and to other users in our region. The CIMC laboratory now provides comprehensive analytic flow cytometry and high-speed cell sorting services, immune function assays including antigen specific and mitogen induced cell proliferation, cytokine production, cell mediated cytotoxicity, and effector T cell frequency. During Phase II, the CIMC also acquired and developed the infrastructure and expertise to study cellular metabolism (of tumor cells and immune cells), including oxygen consumption rate and mitochondrial mass and function; and the detection of immune mediators through multiplex approaches. The state-of-the-art services provided by the CIMC and its experienced team allow the investigators to identify new biomarkers for inflammation, new mechanisms of immune dysfunction in disease, and innovative approaches to overcome immune suppression in diseases characterized by chronic inflammation, thereby increasing their chances for high impact publications and federal and foundation-related funding. These advanced technologies have positioned the CIMC as the leader laboratory in inflammation and immune research in the region, which has resulted in an increased number of users and its integration as a core laboratory at the LSUHSC School of Medicine and the LSU-Cancer Center. The main goal of Phase III is to expand the number of users by providing the most advanced technologies to study inflammation and disease as they become available, and to complete the integration of CIMC as a Cancer Center and School of Medicine Core. Thus, our proposal encompasses the potential of significantly improving the quality of translational research in the State of Louisiana.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Center Core Grants (P30)
Project #
1P30GM114732-01
Application #
8883037
Study Section
Special Emphasis Panel (ZGM1)
Project Start
Project End
Budget Start
2015-07-01
Budget End
2016-06-30
Support Year
1
Fiscal Year
2015
Total Cost
Indirect Cost
Name
Louisiana State Univ Hsc New Orleans
Department
Type
DUNS #
782627814
City
New Orleans
State
LA
Country
United States
Zip Code
70112
Ghonim, Mohamed A; Wang, Jeffrey; Ibba, Salome V et al. (2018) Sulfated non-anticoagulant heparin blocks Th2-induced asthma by modulating the IL-4/signal transducer and activator of transcription 6/Janus kinase 1 pathway. J Transl Med 16:243
Lassak, Adam; Dean, Mathew; Wyczechowska, Dorota et al. (2018) Molecular and Structural Traits of Insulin Receptor Substrate 1/LC3 Nuclear Structures and Their Role in Autophagy Control and Tumor Cell Survival. Mol Cell Biol 38:
Berger, Nathan A; Besson, Valerie C; Boulares, A Hamid et al. (2018) Opportunities for the repurposing of PARP inhibitors for the therapy of non-oncological diseases. Br J Pharmacol 175:192-222
Ungerleider, Nathan A; Rao, Sonia G; Shahbandi, Ashkan et al. (2018) Breast cancer survival predicted by TP53 mutation status differs markedly depending on treatment. Breast Cancer Res 20:115
Serrano-Gómez, Silvia J; Fejerman, Laura; Zabaleta, Jovanny (2018) Breast Cancer in Latinas: A Focus on Intrinsic Subtypes Distribution. Cancer Epidemiol Biomarkers Prev 27:3-10
Sanabria-Salas, María Carolina; Hernández-Suárez, Gustavo; Umaña-Pérez, Adriana et al. (2017) IL1B-CGTC haplotype is associated with colorectal cancer in admixed individuals with increased African ancestry. Sci Rep 7:41920
Loupe, Jacob M; Miller, Patrick J; Crabtree, Judy S et al. (2017) Acquisition of an oncogenic fusion protein is sufficient to globally alter the landscape of miRNA expression to inhibit myogenic differentiation. Oncotarget 8:87054-87072
Rawlik, Konrad; Rowlatt, Amy; Sanabria-Salas, María Carolina et al. (2017) Evidence of epigenetic admixture in the Colombian population. Hum Mol Genet 26:501-508
Al-Khami, Amir A; Zheng, Liqin; Del Valle, Luis et al. (2017) Exogenous lipid uptake induces metabolic and functional reprogramming of tumor-associated myeloid-derived suppressor cells. Oncoimmunology 6:e1344804
Garay, Jone; Piazuelo, M Blanca; Lopez-Carrillo, Lizbeth et al. (2017) Increased expression of deleted in malignant brain tumors (DMBT1) gene in precancerous gastric lesions: Findings from human and animal studies. Oncotarget 8:47076-47089

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