University of California San Francisco

Susana Ortiz-Urda, M.D. Ph.D.
Susana
Ortiz-Urda
MD, PhD

Assistant Professor of Dermatology
Department of Dermatology
Co-Director, UCSF Melanoma Center
UCSF Helen Diller Family Comprehensive Cancer Center

Address

2340 Sutter Street, #N419
San Francisco, CA 94115
United States

Email: [email protected]
Phone: 415-476-8502
Fax: 415-476-8218

    Biography

    Dr. Susana Ortiz-Urda is a dermatologist and melanoma specialist who serves as co-director of the UCSF Melanoma Center. She cares for patients with early and advanced melanoma.

    Ortiz-Urda’s lab works with human models of epithelial neoplasia and melanoma. She studies cancer signaling at a genetic sequencing level to identify novel transcripts, their functions and the factors that promote resistance to drugs or cancer progression. She hopes her findings may point to key biomarkers or new targets for treating melanoma.

    Ortiz-Urda earned her medical degree and doctorate at the University of Vienna. She completed a residency in dermatology and a postdoctoral fellowship in epithelial biology at Stanford University, followed by a cutaneous oncology fellowship at UCSF. She earned her master of business administration degree at New York University.

    Ortiz-Urda is a member of the American Academy of Dermatology, Austrian Society of Dermatology and Venereology, and Dermatology Foundation. She has received several honors, including the Kardinal-Innitzer Award for Outstanding Science in Dermatology and the Unilever Award from the Austrian Society of Dermatology and Venereology.

    Learn more about Ortiz-Urda's research: http://cancer.ucsf.edu/research/ortiz-lab.

    Education

    Institution Degree Dept or School End Date
    New York University, NY M.B.A. Business Administration 2014
    Stanford University Resident Dermatology 2010
    University of California, San Francisco Research Fellowship Derm-Oncology 2010
    The Brooklyn Hospital Center, NY Internship Medicine 2006
    Stanford University Postdoctoral Fellowship Epithelial Biology 2005
    AKH Vienna Research Resident Dermatology 2001
    University of Vienna Research Fellow Dermatology 1999
    Rappersberger, University of Vienna PhD Biology 1998
    University of Vienna M.D. School of Medicine 1998

    Board Certifications

    • American Board of Dermatology

    Clinical Expertise

    Basal Cell Carcinoma
    Squamous Cell Carcinoma
    Skin Cancer in Immunosuppressed Patients
    Melanoma
    Merkel Cell Carcinoma
    Kaposi's sarcoma
    Skin adnexal tumors
    Skin sarcomas
    General Dermatology
    Cutaneous Oncology

    Program Affiliations

    Department of Dermatology
    UCSF Melanoma Center
    Member, UCSF Helen Diller Family Comprehensive Cancer Center

    Research Narrative

    My research interest is centered in the mechanisms involved in cancer progression. In recent studies we studied the role of tumor-stroma interactions in epithelial tumorigenesis. Our goal now is to identify the earliest melanoma precursors and to study the mechanisms of intraepidermal melanoma progression taking advantage of a human tissue model of human melanoma.

    Our laboratory is currently pursuing studies of the signaling and gene regulatory networks that control this process. Our studies are designed to identify potential biomarkers in unresected occult melanoma, establish improved methods to identify occult intraepidermal melanoma, rationalize resection margins, and find treatments to reduce melanoma recurrence at the primary site. My lab is also interested in the epigenetic mechanisms involved in cancer progression and in expression analysis between consecutive stages of tumor progression. These studies are designed to identify targets for genes involved in the migration, proliferation, and invasion of mutant melanocytes.

    Research Interests

    Xenograft models of cutaneous neoplasia

    Mechanisms of cancer progression: signal transduction pathways

    Molecular therapeutics in cancer

    Epigenetics

    Publications

    MOST RECENT PUBLICATIONS FROM A TOTAL OF 48
    1. Poor melanoma outcomes and survival in Asian American and Pacific Islander patients.
      Zheng YJ, Ho C, Lazar A, Ortiz-Urda S| | PubMed
    2. A dual pathway inhibition strategy using BKM120 combined with vemurafenib is poorly tolerated in BRAF V600E/K mutant advanced melanoma.
      Algazi AP, Rotow J, Posch C, Ortiz-Urda S, Pelayo A, Munster PN, Daud A| | PubMed
    3. MEK/CDK4,6 co-targeting is effective in a subset of NRAS, BRAF and 'wild type' melanomas.
      Posch C, Sanlorenzo M, Ma J, Kim ST, Zekhtser M, Ortiz-Urda S| | PubMed
    4. The lincRNA MIRAT binds to IQGAP1 and modulates the MAPK pathway in NRAS mutant melanoma.
      Sanlorenzo M, Vujic I, Esteve-Puig R, Lai K, Vujic M, Lin K, Posch C, Dimon M, Moy A, Zekhtser M, Johnston K, Gho D, Ho W, Gajjala A, Oses Prieto J, Burlingame A, Daud A, Rappersberger K, Ortiz-Urda S| | PubMed
    5. Cutaneous CD56+ T-cell lymphoma developing during pembrolizumab treatment for metastatic melanoma.
      Zheng YJ, Lee A, Pincus L, Ho W, Vujic M, Ortiz-Urda S| | PubMed
    6. Dual MEK/AKT inhibition with trametinib and GSK2141795 does not yield clinical benefit in metastatic NRAS-mutant and wild-type melanoma.
      Algazi AP, Esteve-Puig R, Nosrati A, Hinds B, Hobbs-Muthukumar A, Nandoskar P, Ortiz-Urda S, Chapman PB, Daud A| | PubMed
    7. New insights in melanoma biomarkers: long-noncoding RNAs.
      Moreno-Traspas R, Vujic I, Sanlorenzo M, Ortiz-Urda S| | PubMed
    8. Pharmacological inhibitors of c-KIT block mutant c-KIT mediated migration of melanocytes and melanoma cells in vitro and in vivo.
      Posch C, Moslehi H, Sanlorenzo M, Green G, Vujic I, Panzer-Grümayer R, Rappersberger K, Ortiz-Urda S| | PubMed
    9. Phosphoproteomic Analyses of NRAS(G12) and NRAS(Q61) Mutant Melanocytes Reveal Increased CK2α Kinase Levels in NRAS(Q61) Mutant Cells.
      Posch C, Sanlorenzo M, Vujic I, Oses-Prieto JA, Cholewa BD, Kim ST, Ma J, Lai K, Zekhtser M, Esteve-Puig R, Green G, Chand S, Burlingame AL, Panzer-Grümayer R, Rappersberger K, Ortiz-Urda S| | PubMed
    10. Oncogenic KIT mutations in different exons lead to specific changes in melanocyte phospho-proteome.
      Sanlorenzo M, Vujic I, Posch C, Ma J, Lin K, Lai K, Lee D, Vujic M, Oses-Prieto JA, Chand S, Rodriguez-Peralto JL, Burlingame A, Ortiz-Urda S| | PubMed