The Cancer Cell Biology (CCB) Program of Winship Cancer Institute of Emory University is a laboratory-based translational program focused on understanding the changes in function of human cells as a result of cell transformation. Deregulation of the intra- and extra-cellular functional interactions of the cell's proteome leads to abnormal cell phenotypes, and these processes are at the root of the cancer process. The research within the CCB Program is organized into three scientific themes: (1) Cell Survival and Death Mechanisms, which focuses on intrinsic and extrinsic regulation of cell death through understanding and targeting both the Bcl-2 family and of death receptors; (2) Tumor?Stroma Interactions, which seeks to understand how tumor cells communicate and adhere, the biology of cancer stem cells, angiogenesis and immune interactions, and the process of EMT that is important for cell motility, invasion, and metastasis; and (3) Cancer Cell Metabolism, which focuses on how genetic alterations affecting signaling pathways impact the posttranslational modifications of key metabolic enzymes and redirect metabolic intermediates toward the synthesis of biomolecules of cell growth and proliferation. Under the leadership of Erwin Van Meir, PhD (leader) and Lawrence Boise, PhD (co-leader) the CCB Program has 36 core members from 16 different departments in the School of Medicine or Emory College. Between 2012 and the present, this highly collaborative group of researchers published 541 cancer- relevant scientific articles. Of these, 94 (17%) were intra- and 163 (30%) were inter-programmatic collaborations, and 214 (40%) involved a collaboration with another cancer center or academic organization. As of March 31, 2016, CCB held $17.7 million in annual total cancer-relevant research funding, of which $12.2 million (69%) was awarded directly from the NCI. The scientific advances driven by the CCB Program are highly significant in that they unravel novel mechanisms underlying cancer formation and growth and, in this process, unveil potential therapeutic targets.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA138292-10
Application #
9480804
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
Project End
Budget Start
2018-04-01
Budget End
2019-03-31
Support Year
10
Fiscal Year
2018
Total Cost
Indirect Cost
Name
Emory University
Department
Type
DUNS #
066469933
City
Atlanta
State
GA
Country
United States
Zip Code
30322
Richardson, Alessandra M; Havel, Lauren S; Koyen, Allyson E et al. (2018) Vimentin Is Required for Lung Adenocarcinoma Metastasis via Heterotypic Tumor Cell-Cancer-Associated Fibroblast Interactions during Collective Invasion. Clin Cancer Res 24:420-432
Goldstein, Jordan S; Nastoupil, Loretta J; Han, Xuesong et al. (2018) Disparities in survival by insurance status in follicular lymphoma. Blood 132:1159-1166
Guidot, Daniel M; Switchenko, Jeffrey M; Nastoupil, Loretta J et al. (2018) Surveillance imaging in mantle cell lymphoma in first remission lacks clinical utility. Leuk Lymphoma 59:888-895
Jin, Lingtao; Chun, Jaemoo; Pan, Chaoyun et al. (2018) MAST1 Drives Cisplatin Resistance in Human Cancers by Rewiring cRaf-Independent MEK Activation. Cancer Cell 34:315-330.e7
Chowdhary, Mudit; Okwan-Duodu, Derick; Switchenko, Jeffrey M et al. (2018) Angiotensin receptor blockade: a novel approach for symptomatic radiation necrosis after stereotactic radiosurgery. J Neurooncol 136:289-298
Chen, Zhengjia; Zheng, Youyun; Wang, Zhibo et al. (2018) Interactive calculator for operating characteristics of phase I cancer clinical trials using standard 3+3 designs. Contemp Clin Trials Commun 12:145-153
Halani, Sameer H; Yousefi, Safoora; Vega, Jose Velazquez et al. (2018) Multi-faceted computational assessment of risk and progression in oligodendroglioma implicates NOTCH and PI3K pathways. NPJ Precis Oncol 2:24
Ferris, Matthew J; Liu, Yuan; Ao, Jingning et al. (2018) The addition of chemotherapy in the definitive management of high risk prostate cancer. Urol Oncol 36:475-487
Halicek, Martin; Little, James V; Wang, Xu et al. (2018) Deformable Registration of Histological Cancer Margins to Gross Hyperspectral Images using Demons. Proc SPIE Int Soc Opt Eng 10581:
Cassidy, Richard J; Switchenko, Jeffrey M; El-Deiry, Mark W et al. (2018) Disparities in Postoperative Therapy for Salivary Gland Adenoid Cystic Carcinomas. Laryngoscope :

Showing the most recent 10 out of 331 publications