A Phosphatase Associated with Metastasis of Colorectal Cancer

Author:

Saha Saurabh1,Bardelli Alberto1,Buckhaults Phillip1,Velculescu Victor E.1,Rago Carlo1,Croix Brad St.1,Romans Katharine E.1,Choti Michael A.1,Lengauer Christoph1,Kinzler Kenneth W.1,Vogelstein Bert1

Affiliation:

1. Howard Hughes Medical Institute, The Oncology Center, Department of Surgery, and Program in Cellular and Molecular Medicine, Johns Hopkins Medical Institutions, Baltimore, MD 21231, USA.

Abstract

To gain insights into the molecular basis for metastasis, we compared the global gene expression profile of metastatic colorectal cancer with that of primary cancers, benign colorectal tumors, and normal colorectal epithelium. Among the genes identified, the PRL-3 protein tyrosine phosphatase gene was of particular interest. It was expressed at high levels in each of 18 cancer metastases studied but at lower levels in nonmetastatic tumors and normal colorectal epithelium. In 3 of 12 metastases examined, multiple copies of the PRL-3 gene were found within a small amplicon located at chromosome 8q24.3. These data suggest that the PRL-3 gene is important for colorectal cancer metastasis and provide a new therapeutic target for these intractable lesions.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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