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Xiaoyuan (Shawn) Chen

Contact Information

  • Academic Offices
    Personal Information
    Email shawchen@stanford.edu Tel (650) 725-0950
    Administrative Contact
    Susan Singh Administrative Associate Tel Work 650-736-9781

Administrative Appointments

  • Topical Editor, Nanoscale Research Letters , (2008– present )
  • Editorial Board, European Journal of Nuclear Medicine and Molecular Imaging , (2008– present )
  • Editorial Board, J Nucl Med , (2008– present )
  • Editorial Board, Bioconjugate Chemistry , (2008– present )
  • Editorial Board, Molecular Imaging , (2008– present )
  • Editorial Board, Molecular Imaging and Biology , (2008– present )
  • Editorial Board, The Open Medical Imaging Journal , (2007– present )
  • Editorial Board, Recent Patents on Anti-Cancer Drug Discovery , (2006– present )
  • Editorial Board, Frontiers in Biosciences , (2006– present )
  • Editorial Board, Current Molecular Pharmacology , (2007– present )
  • Editorial Board, Signal Transduction Insights , (2008– present )

Honors and Awards

  • Best Basic Science paper, J Nucl Med (2008)
  • Best Basic Science Awards, SNM Annual Meetings (2006, 2007, 2008)
  • First place award, SNM’s Molecular Imaging Center of Excellence (2008)

Graduate & Fellowship Program Affiliations

Research Interests

We are interested in developing and validating novel molecular imaging probes (nanoparticles, antibodies, proteins, peptides and small organic molecules) for the visualization and quantification of molecular targets that are aberrantly expressed during tumor growth, angiogenesis and metastasis. We are trying to combine both anatomical and molecular imaging techniques to pinpoint molecular and functional information related to tumor growth and dissemination, and monitor specific molecular therapeutic efficacy. We are currently working closely with two important angiogenesis targets: integrin alpha(v)beta(3) and vascular endothelial growth factor receptor subtype-2 (VEGFR-2). Integrins expressed on endothelial cells modulate cell migration and survival during angiogenesis. Integrins expressed on carcinoma cells potentiate metastasis by facilitating invasion and movement across blood vessels. In several malignancies, tumor expression of integrin alpha(v)beta(3) correlates well with tumor progression. VEGF is a key regulator of tumor angiogenesis and is the most potent endothelial cell mitogen. Binding of VEGF to its receptor on the endothelial cell membrane stimulates the VEGF signaling pathway. VEGFR-2 (KDR/Flk-1) is the primary VEGF receptor on endothelial cells. Specific projects include nanoplatform-based molecular imaging, multimodality imaging of angiogenesis and metastasis, as well as targeted delivery of gene, chemo, and radiotherapeutics.

Publications