Colorectal Cancer
Copyright ©The Author(s) 2004. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Sep 15, 2004; 10(18): 2652-2656
Published online Sep 15, 2004. doi: 10.3748/wjg.v10.i18.2652
Comparative study of proteome between primary cancer and hepatic metastatic tumor in colorectal cancer
Bo Yu, Shi-Yong Li, Ping An, Ying-Nan Zhang, Zhen-Jia Liang, Shu-Jun Yuan, Hui-Yun Cai
Bo Yu, Shi-Yong Li, Ping An, Ying-Nan Zhang, Zhen-Jia Liang, Shu-Jun Yuan, Hui-Yun Cai, Department of General Surgery, General Hospital of Beijing Military Command, Beijing 100700, China
Author contributions: All authors contributed equally to the work.
Supported by the National Natural Science Foundation of China, No. 30070747 and No. 30271279
Correspondence to: Bo Yu, Department of General Surgery, General Hospital of Beijing Military Command, Beijing 100700, China. yubo66@126.com
Telephone: +86-10-66721189
Received: July 12, 2003
Revised: July 25, 2003
Accepted: August 16, 2003
Published online: September 15, 2004
Abstract

AIM: To identify the differential proteins associated with colorectal cancer genesis and hepatic metastasis.

METHODS: Hydrophobic protein samples were extracted from normal colorectal mucosa, primary cancer lesion and hepatic metastatic foci of colorectal cancer. With two-dimensional electrophoresis and image analysis, differentially expressed protein spots were detected, and the proteins were identified by matrix assisted laser desorption/ionization-time of flight-mass spectrometry and peptide mass fingerprint analysis.

RESULTS: Significant alterations of the proteins in number and expression levels were discovered in primary cancer and hepatic metastatic foci, the expression of a number of proteins was lost in 25-40 ku, but protein spots was increased in 14-21 ku, compared with normal mucosa. Nine differentially expressed protein spots were identified. Three proteins expressed in normal mucosa, but lost in primary cancer and hepatic metastasis, were recognized as calmodulin, ribonuclease 6 precursor and mannosidase-α. Proapolipoprotein was expressed progressively from normal mucosa to primary cancer and hepatic metastasis. The differentially expressed protein of beta-globin was found in normal mucosa and hepatic metastatic tumor, but lost in primary cancer lesion. Cdc 42, a GTP-binding protein, was identified in hepatic metastasis. The protein spots of C4 from primary cancer, M7 and M9 from hepatic metastasis had less homology with the proteins in database.

CONCLUSION: Variations of hydrophobic protein expression in colorectal cancer initiation and hepatic metastasis are significant and can be observed with two-dimensional electrophoresis. The expression of calmodulin, ribonuclease 6 precursor and mannosidase-α is lost but the expression of proapolipoprotein is enhanced which is associated with colorectal cancer genesis and hepatic metastasis. Cdc 42 and beta-globin are expressed abnormally in hepatic metastasis. Protein C4, M7 and M9 may be associated with colorectal cancer genesis and hepatic metastasis.

Keywords: $[Keywords]