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. Association of Aneuploidy and Flat Dysplasia With Development of High-Grade Dysplasia or Colorectal Cancer in Patients With Inflammatory Bowel Disease.
      Tsai JH, Rabinovitch PS, Huang D, Small T, Mattis AN, Kakar S, Choi WT| | PubMed
    2. Diagnosis and risk stratification of Barrett's dysplasia by flow cytometric DNA analysis of paraffin-embedded tissue.
      Choi WT, Tsai JH, Rabinovitch PS, Small T, Huang D, Mattis AN, Kakar S| | PubMed
    3. Diffusion-weighted imaging of hyperpolarized [13 C]urea in mouse liver.
      Marco-Rius I, Gordon JW, Mattis AN, Bok R, Delos Santos R, Sukumar S, Larson PEZ, Vigneron DB, Ohliger MA| | PubMed
    4. A Novel Tumor-Activated Prodrug Strategy Targeting Ferrous Iron Is Effective in Multiple Preclinical Cancer Models.
      Spangler B, Fontaine SD, Shi Y, Sambucetti L, Mattis AN, Hann B, Wells JA, Renslo AR| | PubMed
    5. Heightened Immune Activation in Fetuses with Gastroschisis May Be Blocked by Targeting IL-5.
      Frascoli M, Jeanty C, Fleck S, Moradi PW, Keating S, Mattis AN, Tang Q, MacKenzie TC| | PubMed
    6. Human stem cells from single blastomeres reveal pathways of embryonic or trophoblast fate specification.
      Zdravkovic T, Nazor KL, Larocque N, Gormley M, Donne M, Hunkapillar N, Giritharan G, Bernstein HS, Wei G, Hebrok M, Zeng X, Genbacev O, Mattis A, McMaster MT, Krtolica A, Valbuena D, Simón C, Laurent LC, Loring JF, Fisher SJ| | PubMed
    7. A screen in mice uncovers repression of lipoprotein lipase by microRNA-29a as a mechanism for lipid distribution away from the liver.
      Mattis AN, Song G, Hitchner K, Kim RY, Lee AY, Sharma AD, Malato Y, McManus MT, Esau CC, Koller E, Koliwad S, Lim LP, Maher JJ, Raffai RL, Willenbring H| | PubMed
    8. Mouse liver repopulation with hepatocytes generated from human fibroblasts.
      Zhu S, Rezvani M, Harbell J, Mattis AN, Wolfe AR, Benet LZ, Willenbring H, Ding S| | PubMed
    9. A ZFN/piggyBac step closer to autologous liver cell therapy.
      Mattis AN, Willenbring H| | PubMed
    10. Expression of glypican-3 in undifferentiated embryonal sarcoma and mesenchymal hamartoma of the liver.
      Levy M, Trivedi A, Zhang J, Miles L, Mattis AN, Kim GE, Lassman C, Anders RA, Misdraji J, Yerian LM, Xu H, Dhall D, Wang HL| | PubMed