Expression and its significance of cyclooxygenase-2 in human renal cell carcinoma
Kang Fu-xi
Abstract
Kang Fu-xi
Abstract
Objective To study the relationship between the expression of cyclooxygenase-2(COX-2) and the carcinogenesis and biological behavior of renal cell carcinoma(RCC). Methods COX-2 expression and microvascular density(MVD) were investigated in 120 cases of RCC specimens and 25 cases of normal kidney tissues by using SP immunohistochemical method. Results The expression of COX-2 was positive in tumor tissues(36.7%) but negative in normal kidney tissues. The expression rate of COX-2 was significantly correlated to the grades and stages of kidney tumors. MVD was higher in patients with COX-2 positive expression than that in patients with COX-2 negative expression(84 ± 18 vs 35 ± 10, t = 19.19, P 0.01). Conclusions The highly increased expression of COX-2 in RCC may promote the development of tumor through its stimulating angiogenesis. So, the inhibition of COX-2 expression may become an alternative method to treat RCC.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Objective To study the relationship between the expression of cyclooxygenase-2(COX-2) and the carcinogenesis and biological behavior of renal cell carcinoma(RCC). Methods COX-2 expression and microvascular density(MVD) were investigated in 120 cases of RCC specimens and 25 cases of normal kidney tissues by using SP immunohistochemical method. Results The expression of COX-2 was positive in tumor tissues(36.7%) but negative in normal kidney tissues. The expression rate of COX-2 was significantly correlated to the grades and stages of kidney tumors. MVD was higher in patients with COX-2 positive expression than that in patients with COX-2 negative expression(84 ± 18 vs 35 ± 10, t = 19.19, P 0.01). Conclusions The highly increased expression of COX-2 in RCC may promote the development of tumor through its stimulating angiogenesis. So, the inhibition of COX-2 expression may become an alternative method to treat RCC.
Key concepts: Renal cell carcinoma, Immunohistochemistry, Angiogenesis, Cyclooxygenase, Carcinogenesis, Kidney, Medicine, Pathology