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Andrew L. Warshaw, M.D.

W. Gerald Austen Professor of Surgery, Department of Surgery, Harvard Medical School

Surgeon-in-Chief and Chairman, Surgery, Massachusetts General Hospital

Contact Info

Andrew Warshaw
Massachusetts General Hospital
55 Fruit Street
Boston, MA, 02114
Mailstop: WHT 506
Phone: 617-726-8254
Fax: 617-726-7593
awarshaw@partners.org

Assistant

Suzanne Williams
Executive Assistant
Surgery
Massachusetts General Hospital
55 Fruit Street
Boston, MA, 02114
Mailstop: White 506
Phone: 617-726-8254
Fax: 617-726-7593
swilliams7@partners.org

DF/HCC Program Affiliation

Gastrointestinal Malignancies

Research Abstract

My laboratory has developed a model of pancreatic cancer in the rat by implantation of the carcinogen DMBA in the pancreas. We are characterizing the genetic mutations which accumulate in the carcinogenesis sequence, attempting to develop from this tumor a cell line and tranplantable cancer in nude mice or inbred strains. We are using the model and other cells lines to study the mechanisms of action of chemotherapeutic agents. We are also trying to replicate the model in mice to allow the use of knockout technology as a tool for dissecting pathogenetic factors.

We have a pancreatic cancer database which we use to study outcomes of treatment, and have a particular focus on staging by laparoscopy, peritoneal cytology, and a newly developed technique for detecting circulating pancreatic cancer cells in the bloodstream.

We are characterizing the genetic mutations (K-ras, P-53, etc.) and molecular factors (i.e. telomerase expression) in a library of pancreatic cystic neoplasms and intraductal papillary-mucinous tumors along the spectrum of their malignancy.

Publications

  • Jimenez RE, Warshaw AL, Rattner DW, Willett CG, McGrath D, Fernandez-del Castillo C.Impact of laparoscopic staging in the treatment of pancreatic cancer.Arch Surg 2000 Apr;135(4):409-14; discussion 414-5.
    10768705
  • Jimenez RE, Warshaw AL, Z'graggen K, Hartwig W, Taylor DZ, Compton CC, Fernández-del Castillo C.Sequential accumulation of K-ras mutations and p53 overexpression in the progression of pancreatic mucinous cystic neoplasms to malignancy.Ann Surg 1999 Oct;23
    10522720