Gastrointestinal Cancer Program The Gastrointestinal (GI) Cancer Program is a team of clinician scientists and translational investigators who work collaboratively towards the goal of reducing the morbidity and mortality of GI cancers. GI cancers account for a substantial portion of cancer related deaths in the US and, in aggregate, are the most common cancer in the US. The most common GI cancers are colorectal cancer (143,000 cases/year), upper GI cancers (17,000 esophageal cancers and 21,000 stomach cancers/year), liver cancer (29,000 cases/year), and pancreatic cancer (44,000 cases/year). Thus, the GI Cancer Program has emphasized esophageal adenocarcinoma, pancreatic cancer, liver cancer, and colorectal cancer. The program has formed multidisciplinary care teams and integrative research teams to provide cutting-edge clinical care that incorporates innovative therapeutic trials into the care plans. Examples of these innovations include stromal directed therapy for pancreatic cancer and state of the art molecular diagnostic assay development. There are 32 members in the program, from two institutions, three schools and 14 different divisions and departments. Research themes of the GI cancer program are focused on: 1) investigation of the molecular features that drive the initiation and progression of upper and lower GI cancers; 2) investigation of the host and tumor factors that govern the behavior of GI cancers; 3) development of novel therapies based on new insights into the behavior of cancers; and 4) development of novel molecular diagnostics for the early detection and treatment of GI cancers. The studies are supported by $3.7M in peer-reviewed funding (direct) of which $2.5M is from the NCI (funding in 2013). Investigators in the GI Cancer Program have published 470 manuscripts, which included 12% intra-programmatic, 44% inter-programmatic, and 17% inter-institutional publications. The high percentage of inter-programmatic publications reflects the broad collaborations of the GI Cancer Program members.
The specific aims of the Gastrointestinal Cancer Program are to: 1) Develop novel biomarker assays that can be used for the prevention and/or early detection of colorectal, esophageal, and pancreatic cancers and for risk-stratification for these cancers and liver cancer. 2) Develop novel therapeutic strategies for the treatment of pancreatic cancers directed at the tumor microenvironment. 3) Determine the molecular alterations in the major GI cancers (esophagus, stomach, pancreas, liver, and colon) and use the molecular profiles to inform and effectively treat the cancers.
|Holly, Mayumi K; Smith, Jason G (2018) Adenovirus infection of human enteroids reveals interferon sensitivity and preferential infection of goblet cells. J Virol :|
|Cheng, Heather H (2018) The resounding effect of DNA repair deficiency in prostate cancer. Urol Oncol 36:385-388|
|Poudel, Kumud R; Roh-Johnson, Minna; Su, Allen et al. (2018) Competition between TIAM1 and Membranes Balances Endophilin A3 Activity in Cancer Metastasis. Dev Cell 45:738-752.e6|
|Eaton, Keith D; Romine, Perrin E; Goodman, Gary E et al. (2018) Inflammatory Gene Polymorphisms in Lung Cancer Susceptibility. J Thorac Oncol 13:649-659|
|Bar, Merav; Flowers, Mary E D; Storer, Barry E et al. (2018) Reversal of Low Donor Chimerism after Hematopoietic Cell Transplantation Using Pentostatin and Donor Lymphocyte Infusion: A Prospective Phase II Multicenter Trial. Biol Blood Marrow Transplant 24:308-313|
|Gauthier, Jordan; Turtle, Cameron J (2018) Insights into cytokine release syndrome and neurotoxicity after CD19-specific CAR-T cell therapy. Curr Res Transl Med 66:50-52|
|Graves, Scott S; Parker, Maura H; Stone, Diane et al. (2018) Anti-Inducible Costimulator Monoclonal Antibody Treatment of Canine Chronic Graft-versus-Host Disease. Biol Blood Marrow Transplant 24:50-54|
|Méndez, Eduardo; Rodriguez, Cristina P; Kao, Michael C et al. (2018) A Phase I Clinical Trial of AZD1775 in Combination with Neoadjuvant Weekly Docetaxel and Cisplatin before Definitive Therapy in Head and Neck Squamous Cell Carcinoma. Clin Cancer Res 24:2740-2748|
|Amundsen, Susan K; Smith, Gerald R (2018) The RecB helicase-nuclease tether mediates Chi hotspot control of RecBCD enzyme. Nucleic Acids Res :|
|Montgomery, Elizabeth T; Noguchi, Lisa M; Dai, James Y et al. (2018) Acceptability of and Adherence to an Antiretroviral-Based Vaginal Microbicide among Pregnant Women in the United States. AIDS Behav 22:402-411|
Showing the most recent 10 out of 1267 publications