The major goal of the Cancer Epidemiology Program (CEP) is to understand the pathogenesis of human cancers at the molecular level through the use of observational and interventional studies in human populations. This effort includes a number of large prospective cohort investigations, case-control studies, population-based cross-sectional studies, and hospital-based projects, to identify etiologic risk factors and cancer biomarkers related to the multiple stages of tumorigenesis. Study populations derive from the Bronx/NYC AECC catchment area and regional/national and international inter-institutional collaborations. The scope of research has increased with faculty recruitment and expanded studies by senior CEP investigators. Substantial progress has been made in several molecular epidemiologic research areas. This includes (i) viral causes of cancer- human papillomavirus, simian virus 40, and hepatitis C virus;(ii) the epidemiology of breast cancer and its precursors;(iii) the role of host immunity including studies on immune compromised patients, immune genes (HLA and KIR), and specific immune responses to viral oncoproteins. New research initiatives include (iv) inflammation and cytokines in the development of colorectal cancer and polyps;(v) risk factors for head/neck cancer;(vi) endocrine-based cancer risk factors such as hyperinsulinemia and insulin-like growth factors (IGF), energy consumption, diabetes and obesity, sex hormones, and (vii) genetic epidemiology - studies of gene polymorphisms (e.g., in the insulin and IGF signaling pathways), variations in gene expression (involving use of mRNA arrays), and epigenetic changes (e.g., DMA methylation). Studies on HPV are being translated into therapeutic (vaccine) and screening approaches for cervical cancer. A Biostatistics Shared Resource was established with several members based in the CEP, with ongoing methodological research. There has been increased research in cancerrelated behaviors - substance abuse (e.g., cigarettes/alcohol), energy consumption/obesity, and exercise, with funded intervention efforts. There are currently 16 program members from 7 academic departments supported by 12 NCI ($2.6M Direct) and 4 other NIH grants. There are five new members. Since the last CCSG review there have been 218 research papers by program members of which 19% represent intraprogrammatic, and 7% interprogrammatic collaborative publications.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA013330-39
Application #
8294872
Study Section
Subcommittee G - Education (NCI)
Project Start
Project End
2013-06-30
Budget Start
2011-07-01
Budget End
2012-06-30
Support Year
39
Fiscal Year
2011
Total Cost
$33,558
Indirect Cost
Name
Albert Einstein College of Medicine
Department
Type
DUNS #
110521739
City
Bronx
State
NY
Country
United States
Zip Code
10461
Van Arsdale, Anne R; Arend, Rebecca C; Cossio, Maria J et al. (2018) Insulin-like growth factor 2: a poor prognostic biomarker linked to racial disparity in women with uterine carcinosarcoma. Cancer Med 7:616-625
Ruiz, Penelope D; Gamble, Matthew J (2018) MacroH2A1 chromatin specification requires its docking domain and acetylation of H2B lysine 20. Nat Commun 9:5143
Rohan, Thomas; Ye, Kenny; Wang, Yihong et al. (2018) MicroRNA expression in benign breast tissue and risk of subsequent invasive breast cancer. PLoS One 13:e0191814
Walters, Ryan O; Arias, Esperanza; Diaz, Antonio et al. (2018) Sarcosine Is Uniquely Modulated by Aging and Dietary Restriction in Rodents and Humans. Cell Rep 25:663-676.e6
Racine, Jeremy J; Stewart, Isabel; Ratiu, Jeremy et al. (2018) Improved Murine MHC-Deficient HLA Transgenic NOD Mouse Models for Type 1 Diabetes Therapy Development. Diabetes 67:923-935
Frimer, Marina; Miller, Eirwen M; Shankar, Viswanathan et al. (2018) Adjuvant Pelvic Radiation ""Sandwiched"" Between Paclitaxel/Carboplatin Chemotherapy in Women With Completely Resected Uterine Serous Carcinoma: Long-term Follow-up of a Prospective Phase 2 Trial. Int J Gynecol Cancer 28:1781-1788
Kale, Abhijit; Ji, Zhejun; Kiparaki, Marianthi et al. (2018) Ribosomal Protein S12e Has a Distinct Function in Cell Competition. Dev Cell 44:42-55.e4
Lee, Chang-Hyun; Kiparaki, Marianthi; Blanco, Jorge et al. (2018) A Regulatory Response to Ribosomal Protein Mutations Controls Translation, Growth, and Cell Competition. Dev Cell 46:456-469.e4
Mao, Serena P H; Park, Minji; Cabrera, Ramon M et al. (2018) Loss of amphiregulin reduces myoepithelial cell coverage of mammary ducts and alters breast tumor growth. Breast Cancer Res 20:131
Mocholi, Enric; Dowling, Samuel D; Botbol, Yair et al. (2018) Autophagy Is a Tolerance-Avoidance Mechanism that Modulates TCR-Mediated Signaling and Cell Metabolism to Prevent Induction of T Cell Anergy. Cell Rep 24:1136-1150

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