Cyclooxygenase-2 Expression and Its Prognostic Significance in Clear Cell Renal Cell Carcinoma

被引:19
|
作者
Lee, Ji Won [2 ]
Park, Jeong Hwan [1 ]
Suh, Ja Hee [1 ]
Nam, Kyung Han [1 ]
Choe, Ji-Young [1 ]
Jung, Hae Yoen [1 ]
Chae, Ji Yoen [1 ]
Moon, Kyung Chul [1 ,3 ]
机构
[1] Seoul Natl Univ, Coll Med, Med Res Ctr, Dept Pathol, Seoul 110799, South Korea
[2] Seoul Natl Univ, Coll Med, Med Res Ctr, Dept Pediat, Seoul 110799, South Korea
[3] Seoul Natl Univ, Coll Med, Med Res Ctr, Kidney Res Inst, Seoul 110799, South Korea
基金
新加坡国家研究基金会;
关键词
Carcinoma; renal cell; Cyclooxygenase; 2; Prognosis; COX-2; EXPRESSION; MOLECULAR PATHOLOGY; INTERFERON-ALPHA; CANCER; INHIBITOR; APOPTOSIS; NEOPLASIA; THERAPY; TUMORS;
D O I
10.4132/KoreanJPathol.2012.46.3.237
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Background: The prognostic value of cyclooxygenase-2 (COX-2) in human renal cell carcinoma (RCC) remains unclear. The purposes of this study are to elucidate the clinical significance of COX-2 in clear cell RCC (CCRCC) and to assess the treatment effect of COX-2 inhibition on CCRCC cell lines. Methods: Using tumor samples obtained from 137 patients who had undergone nephrectomy at Seoul National University Hospital, we evaluated COX-2 expression on immunohistochemistry. Moreover, we performed the cell proliferation assay using 3-(4,5-dimethylthiazol-2yl)2,5-diphenyl-2H tetrazolium bromide (MTT) and cell invasion assay. Thus, we evaluated the effect of meloxicam, an inhibitor of COX-2, in two human CCRCC cell lines. Results: Cancer-specific survival (p = 0.038) and progression-free survival (p = 0.031) were shorter in the COX-2 high expression group. A multivariate logistic regression model showed that COX-2 expression was an independent risk factor for pTNM stage and Fuhrman nuclear grade. The MTT assay revealed that COX-2 inhibition led to the suppression of the proliferation of CCRCC cell lines. Moreover, it also reduced their invasion capacity. Conclusions: This study postulates that COX-2 is a poor prognostic indicator in human CCRCC, suggesting that COX-2 inhibition can be a potential therapy in CCRCC.
引用
收藏
页码:237 / 245
页数:9
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