Review
Copyright ©2008 The WJG Press and Baishideng. All rights reserved.
World J Gastroenterol. Jul 7, 2008; 14(25): 3956-3967
Published online Jul 7, 2008. doi: 10.3748/wjg.14.3956
Evolving management of colorectal cancer
Jochem van der Voort van Zijp, Harald J Hoekstra, Marc D Basson
Jochem van der Voort van Zijp, Department of Radiation Oncology, Leiden University Medical Center, Leiden RC 2333, The Netherlands
Harald J Hoekstra, Department of Surgery, University of Groningen Medical Center, Groningen RB 9700, The Netherlands
Marc D Basson, John D. Dingell VA Medical Center and Wayne State University, Detroit MI 48201, United States
Author contributions: van der Voort van Zijp J performed literature research and wrote the paper, Hoekstra HJ and Basson MD both performed literature research and contributed equally to this paper.
Correspondence to: Jochem van der Voort van Zijp, MD, Department of Radiation Oncology, Leiden University Medical Center, Postbus 9600, Leiden RC 2333, The Netherlands. j.r.n.van_der_voort_van_zijp@lumc.nl
Telephone: +31-71-5263533
Fax: +31-71-5266760
Received: January 28, 2008
Revised: May 10, 2008
Accepted: May 17, 2008
Published online: July 7, 2008
Abstract

This article reviews recent advances in surgical techniques and adjuvant therapies for colorectal cancer, including total mesorectal excision, the resection of liver and lung metastasis and advances in chemoradiation and foreshadows some interventions that may lie just beyond the frontier. In particular, little is known about the intracellular and extracellular cascades that may influence colorectal cancer cell adhesion and metastasis. Although the phosphorylation of focal adhesion kinases and focal adhesion associated proteins in response to integrin-mediated cell matrix binding (”outside in integrin signaling”) is well described, the stimulation of cell adhesion by intracellular signals activated by pressure prior to adhesion represents a different signal paradigm. However, several studies have suggested that increased pressure and shear stress activate cancer cell adhesion. Further studies of the pathways that regulate integrin-driven cancer cell adhesion may identify ways to disrupt these signals or block integrin-mediated adhesion so that adhesion and eventual metastasis can be prevented in the future.

Keywords: Adhesion, Colorectal, Signaling, Cancer, Surgery