COX-2 억제제가 누드마우스에 이식된 위암세포주에서 종양의 성장과 전이에 미치는 영향

초록

Purpose: Tumor invasion and metastasis are known to be extremely important factors in the prognosis of cancer patients. Although recent studies have demonstrated that cyclooxygenase-2 (COX-2) is overexpressed in various cancers including gastric cancer, the mechanisms underlying the contribution of COX-2 to tumorigenesis and tumor promotion remain unclear. Methods: In order to determine the role of COX-2 in tumor growth and metastasis, we investigated COX-2 expression, apoptosis and the expression of E-cadherin, CD44v6, MMP-2 and TIMP-2 in gastric cancer xenografts treated with meloxicam (a selective COX-2 inhibitor). Results: Cells from the MKN45 gastric cancer cell line that overexpress COX-2 were inoculated subcutaneously into athymic mice. Oral administration with meloxicam reduced the tumor volume (P＜0.01), induced apoptosis of cancer cells (P＜0.01), suppressed the proliferation rates (P＜0.01), increased the expression of E-cadhrin (P＜0.05) and reduced the expression of MMP-2 and TIMP-2. Conclusion: The above data showed that COX-2 inhibitors can inhibit tumor growth and suppress metastatic potential by expression of adhesion molecules and suppression of metalloproteinases, suggesting that this inhibitor can be used as an additive anti-cancer drug in cases of stomach cancer with radical resection, although further evaluation is required. (J Korean Surg Soc 2002;62:95-102)

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