Professional Education

  • Doctor of Philosophy, Shanghai Jiaotong University (2011)
  • Master of Science, Shanghai Jiaotong University (2008)
  • Bachelor of Science, Lanzhou University (2003)

Stanford Advisors


All Publications

  • Chimeric TK-NOG Mice: A Predictive Model for Cholestatic Human Liver Toxicity JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS Xu, D., Wu, M., Nishimura, S., Nishimura, T., Michie, S. A., Zheng, M., Yang, Z., Yates, A. J., Day, J. S., Hillgren, K. M., Takeda, S. T., Guan, Y., Guo, Y., Peltz, G. 2015; 352 (2): 274-280


    Due to the substantial interspecies differences in drug metabolism and disposition, drug-induced liver injury (DILI) in humans is often not predicted by studies performed in animal species. For example, a drug (bosentan) used to treat pulmonary artery hypertension caused unexpected cholestatic liver toxicity in humans, which was not predicted by preclinical toxicology studies in multiple animal species. In this study, we demonstrate that NOG mice expressing a thymidine kinase transgene (TK-NOG) with humanized livers have a humanized profile of biliary excretion of a test (cefmetazole) drug, which was shown by an in situ perfusion study to result from interspecies differences in the rate of biliary transport and in liver retention of this drug. We also found that readily detectable cholestatic liver injury develops in TK-NOG mice with humanized livers after 1 week of treatment with bosentan (160, 32, or 6 mg/kg per day by mouth), whereas liver toxicity did not develop in control mice after 1 month of treatment. The laboratory and histologic features of bosentan-induced liver toxicity in humanized mice mirrored that of human subjects. Because DILI has become a significant public health problem, drug safety could be improved if preclinical toxicology studies were performed using humanized TK-NOG.

    View details for DOI 10.1124/jpet.114.220798

    View details for Web of Science ID 000347822200009

    View details for PubMedID 25424997