Original Articles
Copyright ©The Author(s) 1998. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Feb 15, 1998; 4(1): 52-54
Published online Feb 15, 1998. doi: 10.3748/wjg.v4.i1.52
Arylsulfatase, β-galactosidase and lysozyme in gastric cancer cells and its relationship to invasion
Yong-Fen Yi, You-Rong Huang
Yong-Fen Yi, You-Rong Huang, Department of Pathology, Chongqing University of Medical Sciences, Chongqing 400046, China
Yong-Fen Yi, Associate professor of pathology, having 10 papers published, Department of Pathology, Chongqing University of Medical Sciences, Chongqing 400046, China
Author contributions: All authors contributed equally to the work.
Correspondence to: Yong-Fen Yi, Department of Pathology, Chongqing University of Medical Sciences, 1 Yixueyuan Road, Chongqing 400046, China
Telephone: +86-23-68807549
Received: September 10, 1997
Revised: October 12, 1997
Accepted: November 20, 1997
Published online: February 15, 1998
Abstract

AIM: To study the distribution of arylsulfatase, β-galactosidase and lysozyme in gastric cancer cells, and its relationship to differentiation and invasion of gastric cancer cells.

METHODS: Histochemical, immunohistochemical and ruthenium red (RR) electrocytochemical technique for three types of hydrolases and proteoglycans in pericancerous matrix in 33 cases of gastric cancer were observed under light and electron microscopy.

RESULTS: The expression intensities of arylsulfatase, β-glactosidase and lysozyme in mucinous cell carcinomas were more intensive than those in well-differentiated and poorly-differentiated adenocarcinomas ( P < 0.05-0.01). The fibrous tissues smooth muscle and proteoglycans close to the cancer cells were degraded. They were found in the region far from the cancer cells. Expression of three enzymes mentioned above was low in adenocarcinoma cells, and fibrous tissues and RR granules were present and intact near the well-differentiated and poorly-differentiated adenocarcinoma cells.

CONCLUSION: Mucinous cell carcinoma may release various hydrolases into extracellular matrix, inducing degradation of pericancerous matrix and facilitating cancer cell invasion and metastasis.

Keywords: stomach neoplasms, hydrolases, proteoglycans histochemistry, neoplasm invasiveness, arylsulfatase, beta-galactosidase, muramidase