(OVERVIEW) The NIDDK P30 Digestive Diseases Research Core Center at the University of Pennsylvania is called the Center for Molecular Studies in Digestive and Liver Diseases (CMSDLD). Constituted in 1997 and funded continuously since then (with highly successful competitive renewals in 2002, 2007 and 2012), the CMSDLD provides an exceptional platform for basic and translational research in digestive, liver and pancreatic diseases with a vision of understanding human health and ameliorating the public health burden associated with these diseases. This overarching vision is executed through the interrelated missions or Specific Aims of the CMSDLD: (1) to support impactful interdisciplinary and collaborative digestive, liver and pancreatic research through its Members/Associate Members, who span 4 Schools at the University of Pennsylvania, multiple Departments/Centers/Institutes, importantly, Children's Hospital of Philadelphia, as well as institutions within and surrounding Philadelphia; (2) to foster the academic and professional development of its Associate Members; (3) to provide state-of-the art services and technologies through its scientific core facilities (with quality and cost-effectiveness), which in turn support the Members and Associate Members; (4) to oversee innovative enrichment (inclusive of education and mentorship) programs and a highly successful pilot and feasibility grant program; (5) to promote gender, diversity and inclusion as part of our CREED (Clinical care, Research, Education, Encouragement and Diversity) and (6) to collaborate with other Penn Centers/Institutes as well as national universities, academic medical centers, other DDRCCs and the NIH/NIDDK, and conduct outreach with the lay public. Rigor, reproducibility and transparency are also critical aspects of the CMSDLD. The CMSDLD has an administrative structure, or Core, which is overseen by the Dean, and guidance from highly interactive Penn/CHOP leaders, and internal and external advisory boards. The CMSDLD may be viewed as a stem cell, which self-renews and concurrently gives rise to differentiated entities on campus that in turn continue to interact with the CMSDLD: (A) Members who apply for and receive new interdisciplinary grants spawned by the CMSDLD; (B) Penn-CHOP Joint Center in Transitional Medicine (adolescence to adulthood) in digestive, liver and pancreatic medicine; (C) Penn-CHOP Microbiome Program. The Perelman School of Medicine and Children's Hospital of Philadelphia have invested heavily in the CMSDLD and are committed to continue to do so in the next funding cycle. The CMSDLD is positioned to build upon its successes and be a vanguard of research, education and translational clinical care in the future.

Public Health Relevance

(OVERVIEW) The Center for Molecular Studies in Digestive and Liver Diseases (CMSLD) is a DDRCC that seeks to catalyze advances in impactful digestive, liver and pancreatic research. These discoveries are translated to improving patients with digestive, liver and pancreatic diseases through innovations in diagnosis, prognosis and therapy.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
5P30DK050306-23
Application #
9762888
Study Section
Special Emphasis Panel (ZDK1)
Program Officer
Perrin, Peter J
Project Start
1997-07-01
Project End
2022-06-30
Budget Start
2019-07-01
Budget End
2020-06-30
Support Year
23
Fiscal Year
2019
Total Cost
Indirect Cost
Name
University of Pennsylvania
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
042250712
City
Philadelphia
State
PA
Country
United States
Zip Code
19104
Wangensteen, Kirk J; Wang, Yue J; Dou, Zhixun et al. (2018) Combinatorial genetics in liver repopulation and carcinogenesis with a in vivo CRISPR activation platform. Hepatology 68:663-676
Andres, Sarah F; Williams, Kathy N; Rustgi, Anil K (2018) The Molecular Basis of Metastatic Colorectal Cancer. Curr Colorectal Cancer Rep 14:69-79
Serper, M; Forde, K A; Kaplan, D E (2018) Rare clinically significant hepatic events and hepatitis B reactivation occur more frequently following rather than during direct-acting antiviral therapy for chronic hepatitis C: Data from a national US cohort. J Viral Hepat 25:187-197
Avetisyan, Marina; Rood, Julia E; Huerta Lopez, Silvia et al. (2018) Muscularis macrophage development in the absence of an enteric nervous system. Proc Natl Acad Sci U S A 115:4696-4701
Kim, Yong Hoon; Marhon, Sajid A; Zhang, Yuxiang et al. (2018) Rev-erb? dynamically modulates chromatin looping to control circadian gene transcription. Science 359:1274-1277
Costea, Paul I; Hildebrand, Falk; Arumugam, Manimozhiyan et al. (2018) Enterotypes in the landscape of gut microbial community composition. Nat Microbiol 3:8-16
Correnti, Jason M; Gottshall, Lauren; Lin, Annie et al. (2018) Ethanol and C2 ceramide activate fatty acid oxidation in human hepatoma cells. Sci Rep 8:12923
Khalili, Mandana; Shuhart, Margaret C; Lombardero, Manuel et al. (2018) Relationship Between Metabolic Syndrome, Alanine Aminotransferase Levels, and Liver Disease Severity in a Multiethnic North American Cohort With Chronic Hepatitis B. Diabetes Care 41:1251-1259
Qiu, Chengxiang; Huang, Shizheng; Park, Jihwan et al. (2018) Renal compartment-specific genetic variation analyses identify new pathways in chronic kidney disease. Nat Med 24:1721-1731
Shoshkes-Carmel, Michal; Wang, Yue J; Wangensteen, Kirk J et al. (2018) Subepithelial telocytes are an important source of Wnts that supports intestinal crypts. Nature 557:242-246

Showing the most recent 10 out of 700 publications