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Copyright ©2008 The WJG Press and Baishideng. All rights reserved.
World J Gastroenterol. May 21, 2008; 14(19): 2990-2994
Published online May 21, 2008. doi: 10.3748/wjg.14.2990
c-Met targeted therapy of cholangiocarcinoma
Matei P Socoteanu, Frank Mott, Gianfranco Alpini, Arthur E Frankel
Matei P Socoteanu, Frank Mott, Gianfranco Alpini, Arthur E Frankel, Scott & White Hospital and Clinics, 5701 S, Airport Rd, Temple, Texas 76502, United States
Author contributions: Socoteanu MP wrote the article; Frankel AE helped write the article; Mott F and Alpini G oversaw and reviewed the article.
Correspondence to: Arthur E Frankel, Director of Scott & White Cancer Research Institute, 5701 S, Airport Rd, Temple, Texas 76502, United States. afrankel@swmail.sw.org
Telephone: +1-254-7240094
Fax: +1-254-7247682
Received: October 15, 2007
Revised: February 2, 2008
Published online: May 21, 2008
Abstract

Cholangiocarcinoma continues to be a challenging disease to treat. Systemic therapy is used in unresectable disease, disease progression after surgery, and in the palliative setting. Unfortunately, results of multiple phase II trials have rarely yielded positive results. As data on the molecular carcinogenesis of cholangiocarcinoma is developing, we are more able to understand the disease process and can use this understanding to create unique targeted therapies. We reviewed the role of c-Met/hepatocyte growth factor (HGF) in the development of cholangiocarcinoma. Furthermore, we explored the use of the c-Met guided cascade as a target to treat cholangiocarcinoma. We reviewed the current use and options for future development of c-Met agents to treat this disease.

Keywords: Cholangiocarcinoma, c-Met, Chemotherapy, Target therapy