The Biology of Colon Cancer is program remains focused on fundamental cellular and molecularmechanisms of intestinal cell maturation and lineage specific differentiation, and how this establishes andmaintains homeostasis of the intestinal mucosa; genetic and environmental factors, and their interactions,that perturb these processes and alter probability of tumor formation and progression; and approaches toprevent tumorigenesis and treat intestinal cancer. Members utilize novel cell systems in culture, mousegenetic models, and human tissues and subjects in their investigations. All of the members areindependently funded by grants that are highly cancer focused, and most participate in large multidisciplinaryprograms that are jointly funded. During the last funding period, this included an NCI U01 Director'sChallenge grant on molecular markers of relative drug sensitivity in colon cancer, and subsequently an NCIU54 Center grant on nutritional-genetic interactions in intestinal cancer. This joint funding, and a largenumber of joint publications, reflects the extensive interactions and collaborations among members of theProgram. Moreover, members of the Program collaborate widely across the AECC and have made uniqueresources available to other Center members. The Program has continued to grow during the last 5 years,both by promotion from within and recruitment, made possible by support from the AECC and a pilot projectprogram funded by the U54 Center grant. Leonard Augenlicht remains the Leader of this Program.There are currently 12 program members from 8 departments, of whom 11 are primary members, supportedby 15 NCI ($3.7M Direct) and 2 other NIH grants. Five members are new to the program. Since the lastCCSG review there have been 105 cancer-relevant research papers by members of this program of which34% represent intraprogrammatic, and 33% represent interprogrammatic publications.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
2P30CA013330-35
Application #
7506816
Study Section
Subcommittee G - Education (NCI)
Project Start
2007-09-25
Project End
2012-06-30
Budget Start
2007-09-25
Budget End
2008-06-30
Support Year
35
Fiscal Year
2007
Total Cost
$14,023
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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