The Cancer Prevention Program (CPP) is a new program that integrates the previous Behavioral and Health Disparities Research and Clinical Cancer Prevention programs to focus on interventional cancer prevention research. The CPP consists of 49 members from 17 departments and is led by Dr. Powel Brown, who focuses on cancer prevention clinical trials, and 2 co-leaders: Dr. Paul Cinciripini, an expert in smoking cessation, and Dr. Karen Basen-Engquist, who has pioneered exercise and weight-management interventions. The overarching goal of the CPP is to develop cancer prevention interventions and improve health in individuals at risk for cancer and in cancer survivors.
Three specific aims support this primary objective.
In Aim 1, we will discover biological pathways critical for cancer development and target these pathways in preclinical models.
In Aim 2, we will discover critical psychobiological, social, and conditional/situational determinants and predictors of cancer risk behavior to inform future cancer preventive interventions.
In Aim 3, we will develop and test novel therapeutic and behavioral interventions in clinical and community-based trials to reduce cancer risk and promote health in individuals at risk for cancer and cancer survivors. Thirty-five CPP members have annual direct peer- reviewed funding of $12.8M, with $6.2M (48%) from the NCI. CPP members have authored more than 1322 published papers (20% intra-programmatic, 44% inter-programmatic, and 73% external collaborations), of which 31% appeared in journals with IF >5 and 10% appeared in journals with IF >10, including CA Cancer J Clin, N Engl J Med, Lancet, JAMA, and Nature. Members have conducted research that used all 14 of the shared resources. Major accomplishments include the demonstration that ARID1A loss is a common early oncogenic event leading to PARP inhibitor sensitivity and the identification of oncogenic changes in precancerous polyps in patients with hereditary colon cancer syndromes (Aim 1), the discovery of a neural EEG biomarker of reward sensitivity that predicts smoking cessation (Aim 2), and the discovery that varenicline is superior to bupropion in reducing depressive symptoms while quitting and promoting smoking cessation for smokers with low reward sensitivity (Aim 3). Major multi-investigator prevention projects include an NCI-funded preclinical consortium (PREVENT), an NCI-funded clinical cancer prevention consortium (N01 Chemoprevention Consortium), 2 Tobacco Centers of Regulatory Science programs, a U54 to study a genetically informed biomarker (nicotine metabolite ratio) for smoking cessation, and an NRG R01 study of ovarian cancer biomarker modulation by activity and diet. Future goals are to target early oncogenic drivers in cancer prevention trials, develop immune- based cancer prevention strategies, combine energy balance and drug-based prevention strategies, develop adaptive smoking cessation treatment algorithms to assign smokers to pharmacotherapy with the goal of changing clinical practice, and reduce cancer incidence and mortality in Houston, the nation, and the world.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA016672-44
Application #
9997836
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
Project End
Budget Start
2020-07-01
Budget End
2021-06-30
Support Year
44
Fiscal Year
2020
Total Cost
Indirect Cost
Name
University of Texas MD Anderson Cancer Center
Department
Type
DUNS #
800772139
City
Houston
State
TX
Country
United States
Zip Code
77030
Ma, Grace X; Lee, Minsun M; Tan, Yin et al. (2018) Efficacy of a community-based participatory and multilevel intervention to enhance hepatitis B virus screening and vaccination in underserved Korean Americans. Cancer 124:973-982
Peng, Guang; Mills, Gordon B (2018) Surviving Ovarian Cancer: An Affair between Defective DNA Repair and RB1. Clin Cancer Res 24:508-510
Radovich, Milan; Pickering, Curtis R; Felau, Ina et al. (2018) The Integrated Genomic Landscape of Thymic Epithelial Tumors. Cancer Cell 33:244-258.e10
Tetzlaff, Michael T; Nelson, Kelly C; Diab, Adi et al. (2018) Granulomatous/sarcoid-like lesions associated with checkpoint inhibitors: a marker of therapy response in a subset of melanoma patients. J Immunother Cancer 6:14
Tayob, Nabihah; Richardson, Peter; White, Donna L et al. (2018) Evaluating screening approaches for hepatocellular carcinoma in a cohort of HCV related cirrhosis patients from the Veteran's Affairs Health Care System. BMC Med Res Methodol 18:1
Caruso, Joseph A; Duong, Mylinh T; Carey, Jason P W et al. (2018) Low-Molecular-Weight Cyclin E in Human Cancer: Cellular Consequences and Opportunities for Targeted Therapies. Cancer Res 78:5481-5491
Yu, Wangie; Chen, Yunyun; Dubrulle, Julien et al. (2018) Cisplatin generates oxidative stress which is accompanied by rapid shifts in central carbon metabolism. Sci Rep 8:4306
Tanco, Kimberson; Azhar, Ahsan; Rhondali, Wadih et al. (2018) The Effect of Message Content and Clinical Outcome on Patients' Perception of Physician Compassion: A Randomized Controlled Trial. Oncologist 23:375-382
Elimova, Elena; Wang, Xuemei; Qiao, Wei et al. (2018) Actionable Locoregional Relapses after Therapy of Localized Esophageal Cancer: Insights from a Large Cohort. Oncology 94:345-353
Hoadley, Katherine A; Yau, Christina; Hinoue, Toshinori et al. (2018) Cell-of-Origin Patterns Dominate the Molecular Classification of 10,000 Tumors from 33 Types of Cancer. Cell 173:291-304.e6

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