CORE: Cell-Based Assay Screening Services Shared Resource (Cell & in vivo Biology Group) PROJECT SUMMARY The complexity and heterogeneity of cancer requires cell-based technological platforms that enable researchers to uncover key genes, pathways, interactions, and modifications that drive cancer development in order to devise effective and personalized therapeutics. The Cell-Based Assay Screening Service (C-BASS) Shared Resource provides DLDCC members with a unique combination of cutting-edge technologies, advanced instrumentation, and genomic resources. C-BASS houses essential elements for single-gene analyses to whole-genome screens including genome-wide short-hairpin RNA (shRNA) libraries, BiFC-tagged (Bi-molecular Fluorescence Complementation) cDNA libraries and multiple state-of-the-art automated robotic instruments for library manipulation, high-throughput screening for phenotypic analyses, and data processing infrastructure for screens. The Shared Resource is directed Drs. Thomas Westbrook and Dan Liu who have extensive expertise in developing and implementing technologies for genome-wide screens. This combination of expertise and resources greatly facilitates DLDCC investigators in their cancer research efforts. Specific services provided by the C-BASS Shared Resource include (1) performing whole-genome or sub-genome scale BiFC and RNAi screens, (2) utilizing individual cDNA and shRNA vectors, (3) large-scale automated manipulation and preparation of cDNA and shRNA libraries, (4) automated mammalian cell transfection and lentivirus production, (5) high-throughput cell-based assays using automated microscopy or flow cytometry, and (6) data analysis, storage, and management. In the past few months, C-BASS has also added genome- editing services using the CRISPR/Cas9 system. The ever-expanding functionalities of CRISPR/Cas9, which include gene targeting, genome modification, and transcription modulation, promises to be of tremendous added value to DLDCC members. By housing these resources in a single, cohesive facility, C-BASS enables Cancer Center Investigators to employ a variety of genomic and genetic platforms that are often cost- and labor-prohibitive, or simply not feasible for individual researchers.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA125123-12
Application #
9525812
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
Project End
Budget Start
2018-07-01
Budget End
2019-06-30
Support Year
12
Fiscal Year
2018
Total Cost
Indirect Cost
Name
Baylor College of Medicine
Department
Type
DUNS #
051113330
City
Houston
State
TX
Country
United States
Zip Code
77030
Boudreaux, Seth P; Duren, Ryan P; Call, Steven G et al. (2018) Drug targeting of NR4A nuclear receptors for treatment of acute myeloid leukemia. Leukemia :
Sukumaran, Sujita; Watanabe, Norihiro; Bajgain, Pradip et al. (2018) Enhancing the Potency and Specificity of Engineered T Cells for Cancer Treatment. Cancer Discov 8:972-987
Kaochar, Salma; Mitsiades, Nicholas (2018) A Novel Mechanism to Drive Castration-Resistant Prostate Cancer. Trends Endocrinol Metab 29:366-368
Johnston, A N; Bu, W; Hein, S et al. (2018) Hyperprolactinemia-inducing antipsychotics increase breast cancer risk by activating JAK-STAT5 in precancerous lesions. Breast Cancer Res 20:42
Ostrom, Quinn T; Kinnersley, Ben; Wrensch, Margaret R et al. (2018) Sex-specific glioma genome-wide association study identifies new risk locus at 3p21.31 in females, and finds sex-differences in risk at 8q24.21. Sci Rep 8:7352
Chen, Fengju; Zhang, Yiqun; Varambally, Sooryanarayana et al. (2018) Molecular Correlates of Metastasis by Systematic Pan-Cancer Analysis Across The Cancer Genome Atlas. Mol Cancer Res :
Morita, Daisuke; Nishio, Nobuhiro; Saito, Shoji et al. (2018) Enhanced Expression of Anti-CD19 Chimeric Antigen Receptor in piggyBac Transposon-Engineered T Cells. Mol Ther Methods Clin Dev 8:131-140
Bajgain, Pradip; Tawinwung, Supannikar; D'Elia, Lindsey et al. (2018) CAR T cell therapy for breast cancer: harnessing the tumor milieu to drive T cell activation. J Immunother Cancer 6:34
Badr, Hoda; Herbert, Krista; Bonnen, Mark D et al. (2018) Dyadic Coping in Patients Undergoing Radiotherapy for Head and Neck Cancer and Their Spouses. Front Psychol 9:1780
Bollard, Catherine M; Tripic, Tamara; Cruz, Conrad Russell et al. (2018) Tumor-Specific T-Cells Engineered to Overcome Tumor Immune Evasion Induce Clinical Responses in Patients With Relapsed Hodgkin Lymphoma. J Clin Oncol 36:1128-1139

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