Core 1 Abstract Core 1: Cell and Tissue Core The Cell and Tissue Core (Core 1) will provide nearly all of the biological materials required for the wet bench work proposed by the various projects. This will take three forms. 1) The Core will procure, manage, and distribute human liver tissue. This will include cirrhotic and malignant tissue from explant livers removed at the time of liver transplant for hepatocellular carcinoma (HCC) and cirrhosis. Normal liver tissue will also be obtained from liver resections carried out for limited metastatic disease. 2) The Core will establish and maintain rodent models of HCC and liver cirrhosis. 3) The Core will isolate and culture all major primary cells of the liver (including hepatocytes, stromal cells such as fibroblasts and hepatic stellate cells, and endothelial cells and macrophages) on demand. Additionally, the Core will serve as a source of clinical knowledge and expertise for the Project investigators. The association of this Core with PSoC@PENN as a whole will provide significant benefits, including standardization and quality control of biological reagents, increased efficiency and cost savings, and minimization of logistical, access, and regulatory hurdles for Center investigators. Finally, the leadership and staff of the Core will provide specialized technical and clinical expertise that would not be possible for any individual Project to acquire over the project period. This Core will be used heavily by all three proposed projects. 1

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Specialized Center--Cooperative Agreements (U54)
Project #
5U54CA193417-04
Application #
9477609
Study Section
Special Emphasis Panel (ZCA1)
Project Start
Project End
Budget Start
2018-05-01
Budget End
2019-04-30
Support Year
4
Fiscal Year
2018
Total Cost
Indirect Cost
Name
University of Pennsylvania
Department
Type
DUNS #
042250712
City
Philadelphia
State
PA
Country
United States
Zip Code
19104
Lee, Calvin K; de Anda, Jaime; Baker, Amy E et al. (2018) Multigenerational memory and adaptive adhesion in early bacterial biofilm communities. Proc Natl Acad Sci U S A 115:4471-4476
Nair, Praful R; Alvey, Cory; Jin, Xiaoling et al. (2018) Filomicelles Deliver a Chemo-Differentiation Combination of Paclitaxel and Retinoic Acid That Durably Represses Carcinomas in Liver to Prolong Survival. Bioconjug Chem 29:914-927
Huang, Mo; Wang, Jingshu; Torre, Eduardo et al. (2018) SAVER: gene expression recovery for single-cell RNA sequencing. Nat Methods 15:539-542
Ban, Ehsan; Franklin, J Matthew; Nam, Sungmin et al. (2018) Mechanisms of Plastic Deformation in Collagen Networks Induced by Cellular Forces. Biophys J 114:450-461
Smith, Lucas R; Cho, Sangkyun; Discher, Dennis E (2018) Stem Cell Differentiation is Regulated by Extracellular Matrix Mechanics. Physiology (Bethesda) 33:16-25
Holle, Andrew W; Young, Jennifer L; Van Vliet, Krystyn J et al. (2018) Cell-Extracellular Matrix Mechanobiology: Forceful Tools and Emerging Needs for Basic and Translational Research. Nano Lett 18:1-8
Pfeifer, Charlotte R; Xia, Yuntao; Zhu, Kuangzheng et al. (2018) Constricted migration increases DNA damage and independently represses cell cycle. Mol Biol Cell 29:1948-1962
Xia, Yuntao; Ivanovska, Irena L; Zhu, Kuangzheng et al. (2018) Nuclear rupture at sites of high curvature compromises retention of DNA repair factors. J Cell Biol 217:3796-3808
Ramakrishnan, N; Bradley, Ryan P; Tourdot, Richard W et al. (2018) Biophysics of membrane curvature remodeling at molecular and mesoscopic lengthscales. J Phys Condens Matter 30:273001
Chen, Gang; Huang, Alexander C; Zhang, Wei et al. (2018) Exosomal PD-L1 contributes to immunosuppression and is associated with anti-PD-1 response. Nature 560:382-386

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