Colorectal Cancer
Copyright ©The Author(s) 2004. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Feb 15, 2004; 10(4): 545-549
Published online Feb 15, 2004. doi: 10.3748/wjg.v10.i4.545
Expression of thymidine phosphorylase by macrophages in colorectal cancer tissues
Ji-Min Zhang, Takayuki Mizoi, Ken-Ichi Shiiba, Iwao Sasaki, Seiki Matsuno
Ji-Min Zhang, Department of Gastrointestinal Surgery, The Second Hospital of Guangzhou Medical School, Guangzhou 510260, Guangdong Province, China
Takayuki Mizoi, Iwao Sasaki, Seiki Matsuno, Ken-ichi Shiiba, The First Department of Surgery, Tohoku University School of Medicine, Sendai 980-8574, Japan
Author contributions: All authors contributed equally to the work.
Supported by Grants-in-Aid for Scientific Research from the Ministry of Education, Culture, Sports and Technology, Japan
Correspondence to: Ji-Min Zhang, MD, PhD, Department of Gastrointestinal Surgery, the Second Hospital of Guangzhou Medical School, Guangzhou 510260, Guangdong Province, China. arthur@basil.freemail.ne.jp
Telephone: +86-20-34152263 Fax: +86-20-82481695
Received: August 2, 2003
Revised: August 22, 2003
Accepted: September 24, 2003
Published online: February 15, 2004
Abstract

AIM: To detect the thymidine phosphorylase (dThdPase) expression in human colorectal cancer tissues and cells.

METHODS: Forty specimens resected from patients with colorectal cancer were immunohistochemically stained by 654-1, anti-dThdPase monoclonal antibody, PG-M1, anti-macrophage marker CD68 monoclonal antibody. Morphometrical analysis and positive cell counting were performed. In 27 of 40 specimens, dThdPase activity was also assayed by HPLC. Otherwise, the dThdPase level was measured by ELISA in 6 colorectal cancer cell lines, LS174T, Clone A, Colo320, CX-1, Lovo, and MIP101, as well as in 2 macrophage-like cell lines, THP-1 and U937.

RESULTS: dThdPase activity was significantly increased in cancer tissues compared with adjacent normal tissue (P < 0.01). In immunohistochemical analysis, it was confirmed that most cells expressed dThdPase were the stromal cells surrounding cancer nests or along the invasive margin of cancer. Based on their morphometrical characteristics, we found that most of them were tumor-associated macrophages (TAMs). The number of dThdPase-positive stromal cells was significantly correlated with the number of CD68-positive macrophages (r = 0.76, P < 0.0001). By ELISA, 18.2 unit/mg and 19.3 unit/mg of dThdPase protein were detected in THP-1 and U937, but only little was detected in 6 colorectal cancer cell lines.

CONCLUSION: The present data suggest that dThdPase expression is seldom detected in colorectal carcinoma cells. TAM is the most important source of dThdPase in colorectal cancer tissues.

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