The Cancer Epidemiology Program (CEP) is an interdisciplinary research program organized into three scientific areas, each related to a type of cancer risk factor: (1) Viral Risk Factors, (2) Hormonal, Obesity, and Inflammation- Related Risk Factors, and (3) Genetic and Epigenetic Risk Factors. Viral Risk Factor research in the CEP focuses extensively on human papillomavirus (HPV) and its role in anogenital and oral cancers. The CEP has long been a major contributor to HPV research. The goal of this research is to contribute new information important to the development of cancer screening practices, HPV vaccine strategies, and other new prevention and treatment methods. This includes studies of the viral and host factors associated with HPV persistence/progression;biomarkers of cervical and anal pre-cancer/cancer;the effectiveness of HPV vaccines in high risk populations;and the impact of microbicides on risk of HPV infection. In addition. Viral Risk Factor research in CEP addresses the effects of HIV/AIDS on cancer, including studies of the immunologic deficits that drive the relationship of HIV with HPV-related tumorigenesis and risk of other AIDS-associated cancers. Hormonal/Obesity/inflammation research in CEP focuses extensively on the role of the insulin/IGF-axis, sex hormones, adipocytokines, and related pathways in obesity-associated cancers (e.g., colon, breast, prostate, etc.). This includes prospective studies of tumor incidence/recurrence/progression and their relation with circulating and local tissue levels of proteins in these pathways and the expression of their receptors. Given the US obesity epidemic these studies are timely, and will contribute to ongoing efforts to identify biomarkers in these pathways that can be used for patient risk stratification, and/or as targets for chemoprevention and treatment. Genetic and Epigenetic research in CEP focuses extensively on germline and somatic mutations, genetic polymorphisms, DNA methylation, and microRNAs. These studies examine the signaling pathways related to oncogenesis, tumor biomarkers important for selecting and developing targeted therapies, and genetic/epigenetic risk factors that can be used for patient risk stratification. CEP investigators are also conducting methodologic studies to improve the laboratory and statistical tools available for conducting genetic and epigenetic research. The CEP currently has 26 members from 11 departments, of whom 11 are new members, supported by 15 NCI grants ($3.7M Direct), and 11 other peer-reviewed cancer-relevant grants ($2.7M Direct). Since the last CCSG review there have been 414 cancer-relevant research papers in the CEP of which 29% represent intraprogrammatic and 18% represent interprogrammatic publications.

Public Health Relevance

Members of this program study populations to identify risk factors for cancer in order to identify ways of preventing cancer. There is a special interest in: (i) viral infections that cause cancer such as the human papillomavirus that causes cervical cancer, (ii) the role of obesity and diabetes in cancer causation, and (iii) factors that increase the risk of breast cancer. These studies also provide valuable information relevant to the development of guidelines for screening.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA013330-41
Application #
8753328
Study Section
Subcommittee B - Comprehensiveness (NCI)
Project Start
Project End
Budget Start
2014-07-01
Budget End
2015-06-30
Support Year
41
Fiscal Year
2014
Total Cost
Indirect Cost
Name
Albert Einstein College of Medicine
Department
Type
DUNS #
City
Bronx
State
NY
Country
United States
Zip Code
10461
Willis, Ian M; Moir, Robyn D; Hernandez, Nouria (2018) Metabolic programming a lean phenotype by deregulation of RNA polymerase III. Proc Natl Acad Sci U S A 115:12182-12187
Hayama, Ryo; Sparks, Samuel; Hecht, Lee M et al. (2018) Thermodynamic characterization of the multivalent interactions underlying rapid and selective translocation through the nuclear pore complex. J Biol Chem 293:4555-4563
Martynova, Elena; Bouchard, Maxime; Musil, Linda S et al. (2018) Identification of Novel Gata3 Distal Enhancers Active in Mouse Embryonic Lens. Dev Dyn 247:1186-1198
Huang, Kezhen; Mukherjee, Subhajit; DesMarais, Vera et al. (2018) Targeting the PXR-TLR4 signaling pathway to reduce intestinal inflammation in an experimental model of necrotizing enterocolitis. Pediatr Res 83:1031-1040
Bines, Jose; Tevaarwerk, Amye J (2018) Baby steps: Pregnancy outcomes after human epidermal growth factor receptor 2-targeted therapy. Cancer :
Mathew, Deepti; Wang, Yanhua; Van Arsdale, Anne et al. (2018) Expression of ?V-Tubulin in Secretory Cells of the Fallopian Tube Epithelium Marks Cellular Atypia. Int J Gynecol Cancer 28:363-370
Mao, Kai; Quipildor, Gabriela Farias; Tabrizian, Tahmineh et al. (2018) Late-life targeting of the IGF-1 receptor improves healthspan and lifespan in female mice. Nat Commun 9:2394
Entenberg, David; Voiculescu, Sonia; Guo, Peng et al. (2018) A permanent window for the murine lung enables high-resolution imaging of cancer metastasis. Nat Methods 15:73-80
Iqbal, Niloy Jafar; Lu, Zhonglei; Liu, Shun Mei et al. (2018) Cyclin-dependent kinase 4 is a preclinical target for diet-induced obesity. JCI Insight 3:
Sharma, Yogeshwar; Liu, Jinghua; Kristian, Kathleen E et al. (2018) In Atp7b-/- Mice Modeling Wilson's Disease Liver Repopulation with Bone Marrowderived Myofibroblasts or Inflammatory Cells and not Hepatocytes is Deleterious. Gene Expr :

Showing the most recent 10 out of 1508 publications