Core C is the animal core. The core will provide technical service to preclinical projects 1, and 2 establishingsubcutaneous and systemic tumor models, assessing uptake of radiolabeled agents, determining therapeuticefficacy of radiolabeled antibody conjugates and haptens, and identifying toxicity associated with single and multimodaltreatment protocols. It will also collect blood for toxicity assessments and tissue for the histological analysis.by Core E. It will use 2 F/T technicians to manage 2160-2560 mice per year in its AAALAC-accredited facility.Specifically it will be responsible for the following tasks: (a) developing new tumor models in untreated andimmunosuppressed mice, (b) injecting cultured tumor cells intravenously or subcutaneously in SCID mice or nudemice, (c) dosing animals with appropriate therapeutic agents [e.g., bispecific antibodies, radiolabeled haptens,radioantibodies, naked antibodies, and chemotherapeutics], (d) monitoring survival, body weight changes and onsetof hind-leg paralysis in systemic tumor models and measuring tumor size of subcutaneous tumors by 3D calipermeasurements, (e) performing biodistribution studies, (f) providing fixed samples of tumors and tissues for histologyto monitor viability and to monitor expression of antigens by immunohistology and for microautoradiography studies,(g) collecting blood samples for white blood cell and platelet enumeration and for measurement of cardiac troponin inproject 4, (h) entering all data (biodistribution, therapy, WBC/Plt, body weight) into Excel spreadsheets, and (i)setting up immunoscintigraphy studies.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
5P01CA103985-04
Application #
7728853
Study Section
Subcommittee G - Education (NCI)
Project Start
2008-08-01
Project End
2009-07-31
Budget Start
2008-08-01
Budget End
2009-07-31
Support Year
4
Fiscal Year
2008
Total Cost
$195,052
Indirect Cost
Name
Center for Molecular Medicine/Immunology
Department
Type
DUNS #
118870583
City
Morris Plains
State
NJ
Country
United States
Zip Code
07950
Smith, Mitchell R; Jin, Fang; Joshi, Indira (2014) Milatuzumab and veltuzumab induce apoptosis through JNK signalling in an NF-?B dependent human transformed follicular lymphoma cell line. Br J Haematol 165:151-3
Binsky-Ehrenreich, I; Marom, A; Sobotta, M C et al. (2014) CD84 is a survival receptor for CLL cells. Oncogene 33:1006-16
Chen, X; Chang, C-H; Stein, R et al. (2012) The humanized anti-HLA-DR moAb, IMMU-114, depletes APCs and reduces alloreactive T cells: implications for preventing GVHD. Bone Marrow Transplant 47:967-80
Alinari, Lapo; Yu, Bo; Christian, Beth A et al. (2011) Combination anti-CD74 (milatuzumab) and anti-CD20 (rituximab) monoclonal antibody therapy has in vitro and in vivo activity in mantle cell lymphoma. Blood 117:4530-41
Brem, Elizabeth A; Thudium, Karen; Khubchandani, Sapna et al. (2011) Distinct cellular and therapeutic effects of obatoclax in rituximab-sensitive and -resistant lymphomas. Br J Haematol 153:599-611
Sharkey, Robert M; Goldenberg, David M (2011) Cancer radioimmunotherapy. Immunotherapy 3:349-70
Stein, Rhona; Balkman, Cheryl; Chen, Susan et al. (2011) Evaluation of anti-human leukocyte antigen-DR monoclonal antibody therapy in spontaneous canine lymphoma. Leuk Lymphoma 52:273-84
Rossi, Edmund A; Rossi, Diane L; Cardillo, Thomas M et al. (2011) Preclinical studies on targeted delivery of multiple IFN?2b to HLA-DR in diverse hematologic cancers. Blood 118:1877-84
Stein, Rhona; Gupta, Pankaj; Chen, Xiaochuan et al. (2010) Therapy of B-cell malignancies by anti-HLA-DR humanized monoclonal antibody, IMMU-114, is mediated through hyperactivation of ERK and JNK MAP kinase signaling pathways. Blood 115:5180-90
Binsky, Inbal; Lantner, Frida; Grabovsky, Valentin et al. (2010) TAp63 regulates VLA-4 expression and chronic lymphocytic leukemia cell migration to the bone marrow in a CD74-dependent manner. J Immunol 184:4761-9

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