Abstract

It has recently been recognized that inflammatory cytokines, such as tumor necrosis factor-α (TNF-α), upregulate the secretion of matrix metalloproteinase-9 (MMP-9) from cancer cells and thereby promote peritoneal dissemination. In this study, we found that TNF-α also stimulated peritoneal mesothelial cells to secrete MMP-9 as assessed by zymography. MMP-9 gene expression in mesothelial cells induced by TNF-α was confirmed by quantitative RT-PCR analysis. We then utilized the reconstituted artificial mesothelium, which was composed of a monolayer of mesothelial cells cultured on a Matrigel layer in a Boyden chamber system, to examine the effects of TNF-α on carcinoma cell invasion. The transmigration of MKN1 human gastric carcinoma cells through the reconstituted mesothelium was promoted by TNF-α in a dose-dependent manner. The increased MKN1 cell migration was partially inhibited by the anti-α3 integrin antibody, indicating that the invasion process involves an integrin-dependent mechanism. Finally, we observed that the invasion of MMP-9-knockdown MKN1 cells into Matrigel membranes was potentiated by the exogenous addition of purified proMMP-9. These results suggest that TNF-α-induced MMP-9 secretion from mesothelial cells plays an important role in the metastatic dissemination of gastric cancer.

Highlights

  • Metastatic peritoneal dissemination causes a poor prognosis for patients with advanced gastric cancer

  • We have studied the interaction of gastric carcinoma cells with the extracellular matrix (ECM) deposited by peritoneal mesothelial cells and found that MKN1 human gastric carcinoma cells secreted matrix metalloproteinase-9 (MMP-9) accompanied by enhanced invasion through Matrigel-reconstituted basement membranes when these cells adhered to ECM containing laminin-332, a major component of submesothelial basement membranes [15]

  • We first examined the effects of tumor necrosis factor-α (TNF-α) on matrix metalloproteinases (MMPs)-9 secretion in the co-cultures of MKN1 and peritoneal mesothelial cells

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Summary

Introduction

Metastatic peritoneal dissemination causes a poor prognosis for patients with advanced gastric cancer. We have studied the interaction of gastric carcinoma cells with the extracellular matrix (ECM) deposited by peritoneal mesothelial cells and found that MKN1 human gastric carcinoma cells secreted MMP-9 accompanied by enhanced invasion through Matrigel-reconstituted basement membranes when these cells adhered to ECM containing laminin-332, a major component of submesothelial basement membranes [15]. We present evidence showing that MMP-9 secreted from mesothelial cells plays a significant role in the invasion of gastric carcinoma cells. For this purpose, we used a reconstituted mesothelium consisting of peritoneal mesothelial cells and Matrigel basement membranes in a Boyden chamber system

Mesothelial Cells Secreted MMP-9 in Response to Stimulation with TNF-α
The Exogenous Addition of MMP-9 Promotes MKN1 Cell Invasion
Discussion
Reagents
Gelatin Zymography
Cell Invasion Assay Using Reconstituted Mesothelium
Cell Adhesion Assay
Flow Cytometry
MMP-Knockdown MKN1 Cells
Purification of MMP-9
Full Text
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