University of California San Francisco

Mattis 144.jpg
Aras N. Mattis, MD, PhD

Assistant Professor, UCSF Department of Pathology

Address

513 Parnassus Avenue, HSW, #516
San Francisco, CA 94143
United States

Email: [email protected]
Phone: 415-514-3062

    Biography

    Aras N. Mattis, M.D., Ph.D., is a board-certified anatomic pathologist and clinical fellow in the Willenbring Lab. Dr. Mattis trained at the University of Illinois at Urbana-Champaign, earning both his doctorates, Biochemistry and Medicine, there in 2007. He continued his clinical training in Pathology at the University of California San Francisco completing residency in Anatomic Pathology with subsequent fellowship training in Surgical Pathology and Liver and gastrointestinal pathology under his clinical mentor, Dr. Linda Ferrell. Since 2010, he has worked in the Willenbring Lab, investigating the basic mechanisms of liver development and disease in the with a specific focus on liver metabolism and fatty liver disease as well as micro-RNA regulation of liver metabolism.

    Education

    Institution Degree Dept or School End Date
    University of Illinois Urbana-Champaign PhD Biochemistry 2007
    University of Illinois Urbana-Champaign MD Medicine 2007
    University of California Berkeley BA Molecular and Cell Biology - Genetics 1998

    Board Certifications

    American Board of Pathology, Anatomic Pathology

    Collaboration Interests

    I am interested in:

    • academic collaboration
    • academic senate committee service
    • companies and entrepreneurs
    • multicenter clinical research
    • press
    • prospective donors

    Clinical Expertise

    Liver and Gastrointestinal Pathology

    Program Affiliations

    UCSF Department of Pathology

    California Institute for Regenerative Medicine

    Grants and Funding

    • Establishing patient-derived iPSCs as a platform for discovery research in NAFLD | NIDDK | 2023-06-01 - 2028-05-30 | Role: MPI
    • Modeling and Characterization of NAFLD Phenotypes in a Severely Affected Family | NIH/NIDDK | 2024-02-01 - 2027-11-30 | Role: PI
    • Genetic Regulation of Nonalcoholic Fatty Liver Disease | NIH | 2021-06-08 - 2025-03-31 | Role: MPI
    • Regulation of Lipid Metabolism by miR-29a within Hepatocytes | NIH | 2013-09-01 - 2019-07-31 | Role: Principal Investigator

    Research Narrative

    Dr. Mattis' postdoctoral work includes the use of translational human biopsy material as well as patient-derived induced pluripotent stem cell reprogramming to hepatocytes. As a long-term goal, this work aims to develop a humanized liver mouse model of fatty liver disease. Aras is supported by the UCSF CIRM clinical fellow training grant and continues to work closely with the UCSF Department of Pathology as a clinical researcher.

    Research Interests

    Liver diseases including metabolic, pediatric, fibrotic, idiopathic, stem cell derived

    Hepatocytes for transplant and disease modeling, micro-RNA regulation of hepatocyte

    Development and metabolism, liver and gastrointestinal tumors, site-specific recombination.

    Publications

    MOST RECENT PUBLICATIONS FROM A TOTAL OF 56
    1. AAV capsid prioritization in normal and steatotic human livers maintained by machine perfusion.
      Kim JJ, Kurial SNT, Choksi PK, Nunez M, Lunow-Luke T, Bartel J, Driscoll J, Her CL, Dhillon S, Yue W, Murti A, Mao T, Ramos JN, Tiyaboonchai A, Grompe M, Mattis AN, Syed SM, Wang BM, Maher JJ, Roll GR, Willenbring H| | PubMed
    2. Predicting Metabolic Dysfunction Associated Steatotic Liver Disease Risk Using Patient-Derived Induced Pluripotent Stem Cells.
      Qin Y, Chhetri P, Theusch E, Lim G, Teker S, Kuang YL, Aziziraftar SK, Mehraban MH, Munoz-Howell A, Saxena V, Le Guillou D, Mattis AN, Maher JJ, Medina MW| | PubMed
    3. Fluoride-related changes in the fetal cord blood proteome; a pilot study.
      Tuomivaara ST, Fisher SJ, Hall SC, Goin DE, Mattis AN, Den Besten PK| | PubMed
    4. Human Hepatocytes Can Give Rise to Intrahepatic Cholangiocarcinomas.
      Hsu BY, Driscoll J, Human Cholangiocarcinogenesis Project, Tateno C, Mattis AN, Kelley RK, Willenbring H| | PubMed
    5. MicroRNAs Associated with Metformin Treatment in the Diabetes Prevention Program.
      Lewis KA, Stroebel BM, Zhang L, Aouizerat B, Mattis AN, Flowers E| | PubMed
    6. AMPK stimulation inhibits YAP/TAZ signaling to ameliorate hepatic fibrosis.
      Shihan MH, Sharma S, Cable C, Prathigudupu V, Chen A, Mattis AN, Chen JY| | PubMed
    7. Fluoride-related changes in the fetal cord blood proteome; a pilot study.
      Tuomivaara ST, Goin DE, Fisher SJ, Hall SC, Mattis AN, Den Besten PK| | PubMed
    8. MicroRNAs Associated with Metformin Treatment in the Diabetes Prevention Program.
      Lewis KA, Stroebel B, Zhang L, Aouizerat B, Mattis A, Flowers E| | PubMed
    9. Hyperpolarized [1-13 C] pyruvate MRSI to detect metabolic changes in liver in a methionine and choline-deficient diet rat model of fatty liver disease.
      Piraquive Agudelo J, Kim Y, Agarwal S, Sriram R, Bok R, Kurhanewicz J, Mattis AN, Maher JJ, von Morze C, Ohliger MA| | PubMed
    10. Group 2 innate lymphoid cells constrain type 3/17 lymphocytes in shared stromal niches to restrict liver fibrosis.
      Sbierski-Kind J, Cautivo KM, Wagner JC, Dahlgren MW, Nilsson J, Krasilnikov M, Mroz NM, Lizama CO, Gan AL, Matatia PR, Taruselli MT, Chang AA, Caryotakis S, O'Leary CE, Kotas M, Mattis AN, Peng T, Locksley RM, Molofsky AB| | PubMed