The aim of clinical trials and research support core (Core C) is to provide the infrastructure and support at DF/HCC to facilitate translation of the research findings from this Program into clinical research to make advances in the treatment of lymphoma. This includes clinical trials support and development, data management, research nurse support sample trafficking, collection, and processing, providing laboratory based endpoint analysis including assessment of minimal residual disease assessment necessary to 1) perform clinical translational research studies in patients with NHL, 2) prepare translational research protocols for experimental treatment approaches, 3) obtain specimens with appropriate consent from patients, 4) distribute specimens to the appropriate laboratory studies within the PROGRAM PROJECT, 5) provide necessary clinical information to characterize the lymphoma samples being analyzed within the Projects, 6) perform molecular assessment of immunoglobulin gene rearrangements and non random chromosomal translocations in lymphoma samples, and 7) perform follow-up studies of detection of minimal residual disease where appropriate. It will also be instrumental in developing technology to nurture and support future clinical trials. It therefore, includes clinical data management and its inter-relation with laboratory data management, specimen tracking, clinical research study coordination and administrative functions related to conduct of clinical research studies. In addition, it will provide laboratory support for immunologic and molecular biologic monitoring of lymphoma patients in innovative treatment approaches. The Core will provide sequences of chromosomal translocations in lymphoma to Project 1. It is highly interactive with the Biostatistical Core D to design clinical trails and to ensure Quality Control procedures for all patient related data throughout the Program. It includes facilities that are needed to conduct clinical research studies and is highly interactive with Project 5 and will function to translate to the clinical arena advances made within Projects 1, 2, 3, 4, and 5.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
1P01CA092625-01
Application #
6493435
Study Section
Subcommittee E - Prevention &Control (NCI)
Project Start
2001-08-02
Project End
2006-06-30
Budget Start
Budget End
Support Year
1
Fiscal Year
2001
Total Cost
Indirect Cost
Name
Dana-Farber Cancer Institute
Department
Type
DUNS #
149617367
City
Boston
State
MA
Country
United States
Zip Code
02115
Chapuy, Bjoern; Cheng, Hongwei; Watahiki, Akira et al. (2016) Diffuse large B-cell lymphoma patient-derived xenograft models capture the molecular and biological heterogeneity of the disease. Blood 127:2203-13
Carey, Christopher D; Gusenleitner, Daniel; Chapuy, Bjoern et al. (2015) Molecular classification of MYC-driven B-cell lymphomas by targeted gene expression profiling of fixed biopsy specimens. J Mol Diagn 17:19-30
Zhang, Baochun; Calado, Dinis Pedro; Wang, Zhe et al. (2015) An oncogenic role for alternative NF-?B signaling in DLBCL revealed upon deregulated BCL6 expression. Cell Rep 11:715-26
Gostissa, Monica; Bianco, Julia M; Malkin, Daniel J et al. (2013) Conditional inactivation of p53 in mature B cells promotes generation of nongerminal center-derived B-cell lymphomas. Proc Natl Acad Sci U S A 110:2934-9
Yan, Qingsheng; Xu, Rong; Zhu, Liya et al. (2013) BAL1 and its partner E3 ligase, BBAP, link Poly(ADP-ribose) activation, ubiquitylation, and double-strand DNA repair independent of ATM, MDC1, and RNF8. Mol Cell Biol 33:845-57
Ying, Carol Y; Dominguez-Sola, David; Fabi, Melissa et al. (2013) MEF2B mutations lead to deregulated expression of the oncogene BCL6 in diffuse large B cell lymphoma. Nat Immunol 14:1084-92
Chen, Linfeng; Monti, Stefano; Juszczynski, Przemyslaw et al. (2013) SYK inhibition modulates distinct PI3K/AKT- dependent survival pathways and cholesterol biosynthesis in diffuse large B cell lymphomas. Cancer Cell 23:826-38
Rossi, Davide; Rasi, Silvia; Spina, Valeria et al. (2013) Integrated mutational and cytogenetic analysis identifies new prognostic subgroups in chronic lymphocytic leukemia. Blood 121:1403-12
Monti, Stefano; Chapuy, Bjoern; Takeyama, Kunihiko et al. (2012) Integrative analysis reveals an outcome-associated and targetable pattern of p53 and cell cycle deregulation in diffuse large B cell lymphoma. Cancer Cell 22:359-72
Cohen, Nicole A; Stewart, Michelle L; Gavathiotis, Evripidis et al. (2012) A competitive stapled peptide screen identifies a selective small molecule that overcomes MCL-1-dependent leukemia cell survival. Chem Biol 19:1175-86

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