Professional Activities:

Positions and Honors

2007-2011 Postdoctoral Research Fellow Stanford University School of Medicine/Hematology Department
2012-Present Research Associate Stanford University School of Medicine/Hematology Department

Awards & Honors

National Cancer Institute-UO1 Grant Functional analysis of oncogenic networks in primary organoids (2012-Present)
National Institutes of Health (NIH) RO1 Grant Wnt and Hh Signaling Pathways in Adult Physiology (2009-2012)
Dean’s Fellowship Stanford University (2007-2008)
Doctoral Scholarship University of Alabama at Birmingham (2000-2006)
First Prize, Award for Academic Excellence China Agricultural University (1996-1999)
Third Prize, Award for Academic Excellence China Agricultural University (1995)

Relevant Experience

Stanford University School of Medicine/Hematology Department (2012-Present)

Research Scientist
  • Accomplished the first in vitro oncogenic transformation of primary colon,  gastric and pancreatic  tissue to adenocarcinoma with in vivo tumorigenicity
  • Developed an in vitro functional validation system using primary organoid culture for selected  oncogenic driver candidates of gastrointestinal cancer based on bioinformatics analysis of cancer genomic databases.
  • Investigated mechanism of identified oncogenic drivers.
  • Improving the functional validation system toward high-throughput screening for therapeutic drug discovery utilizing 96-well formatted primary cell-based selection, flow cytometry, proliferation and  invasion assays.

Stanford University School of Medicine/Hematology Department (2007-2011)

Postdoctoral Research Fellow

  • Built a retrovirus library of selected colorectal cancer candidate drivers
  • In vitro modeling of colorectal cancer using a robust long-term methodology of primary mouse intestinal organoid culture.
  • Investigated intestinal stem cell /cancer stem (LGR5+) cell biology utilizing primary intestinal culture.

University of Alabama-Birmingham, Comprehensive Cancer Center (2000-2006)

Graduate Student Scientist

  • Generated a Gli1 conditional expression mouse model for basal cell carcinoma (BCC) to investigated downstream mechanisms underlying Shh-Gli1-meidated transformation.
  • Identified Snail as a limiting factor of Gli1-induced transformation in vitro and an early response gene of Gli1-mediated basal cell carcinoma (BCC).
  • Determined a role of Wnt signaling pathway in Gli1-Snail-mediated tumorigenesis.

Chinese Academy of Sciences (C.A.S), Institute of Microbiology (1999-2000)

Research Assistant

  • Characterized two insect-resistant genes in homozygous cotton lines.

 

Xingnan Li

Research Associate

 

  • : (650) 714-8945

  • DEPARTMENTDepartment of Hematology
    Stanford University School of Medicine
  • COUNTRY USA