Key Documents
Chris Cartwright, MD
Academic Appointments
- Professor, Medicine - Gastroenterology & Hepatology
- Member, Cancer Center
Contact Information
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Clinical Offices
Gastroenterology Clinic 300 Pasteur Dr A175 MC 5309 Stanford, CA 94305 Tel Work (650) 723-6961 Fax (650) 725-8418
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Academic Offices
Administrative Contact Georgia Giatras GI Administrator Email Tel Work 650-498-5211Not for medical emergencies or patient use
Professional Snapshot
Clinical Focus
- Ulcerative Colitis
- Crohn's Disease
- Cancer in Inflammatory Bowel Diseases
- Gastroenterology
Administrative Appointments
- Director, Program for Inflammatory Bowel Diseases, Stanford University School of Medicine (1989 - present)
Honors and Awards
- Outstanding AGA Women in Science, American Gastroenterological Association (2008)
- Premier Physician Award, Crohn's & Colitis Foundation of America - Greater Bay Area Chapter (2000)
- Member, American Society for Clinical Investigation (1995)
Professional Education
| Board Certification: | Gastroenterology, American Board of Internal Medicine (1987) |
| Fellowship: | UCSD Medical Center, CA (1984) |
| Board Certification: | Internal Medicine, American Board of Internal Medicine (1981) |
| Residency: | UCSD Medical Center, CA (1981) |
| Internship: | UCSD Medical Center, CA (1979) |
Postdoctoral Advisees
Graduate & Fellowship Program Affiliations
Community & International Work
Scientific Focus
Research Interests
Research in my laboratory focuses on molecular mechanisms of intestinal cell growth control. A primary focus is on function and regulation of the Src family of tyrosine kinases in normal cells, and their deregulation in cancer cells. Molecular, cellular and physiologic approaches are used to explore basic questions about growth regulation. Areas of active investigation include studies of Src function in cell cycle progression, proliferation, differentiation, adhesion, survival and malignant transformation; discovery of endogenous inhibitors of Src kinases; analysis of inhibitor function in cell growth control and apoptosis; and exploration of new drug therapy for colon cancer. Our recent discovery of a Src inhibitor, RACK1, which works both to inhibit growth (by suppressing Src activity at G1 and mitotic checkpoints) and to induce death of colon cells, could be exploited for development of new and more powerful and selective strategies for treatment of human colon cancer.
Publications
- Crohn's colitis complicated by cytomegalovirus infection. Dig Dis Sci. 2009; (9): 1864-7
- A novel pro-apoptotic function of RACK1: suppression of Src activity in the intrinsic and Akt pathways. Oncogene. 2009
- RACK1 inhibits colonic cell growth by regulating Src activity at cell cycle checkpoints. Oncogene. 2007; (20): 2914-24
- Peptide modulators of Src activity in G1 regulate entry into S phase and proliferation of NIH 3T3 cells. Biochem Biophys Res Commun. 2007; (2): 423-30
- Cytomegalovirus infection in steroid-refractory ulcerative colitis: a case-control study. Am J Surg Pathol. 2004; (3): 365-73

