肾细胞癌中COX-2表达的评估及其与临床病理因素的相关性:组织芯片研究

G. Ashour, W. Said
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摘要

目的:本研究旨在评估COX-2在肾细胞癌中的表达,并将其与不同患者的临床病理资料相关联,强调COX-2作为肾细胞癌预后因素的作用,并决定哪些病例更可能从后续的靶向治疗中获益。患者和方法:本系列包括47例患者的组织样本(男性30例,女性17例)。所有肿瘤样本均于2009年7月至2010年11月在亚历山大大学医学院病理学系采集。采用档案石蜡包埋肾细胞癌组织标本制备组织微阵列块,用COX-2抗体进行免疫组化染色。标记物表达被分类进行统计分析,然后与临床病理变量相关。结果:组织学类型与COX-2的表达有显著相关性,乳头状型和憎色型肾细胞癌中COX-2的高表达多见于1分和2分的肾细胞癌,透明细胞型肾细胞癌中COX-2的表达多为0分和1分。结论:COX-2标志物的表达与肿瘤的组织学类型有关;COX-2表达研究可提供肿瘤侵袭性的预后信息。这些发现提示COX-2靶向治疗对COX-2过表达肾细胞癌的潜在影响有待进一步研究。
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Evaluation of COX-2 expression in renal cell carcinoma and its correlation with clinicopathological factors: a tissue microarray study
Objectives: This study, aimed to evaluate the expression of COX-2 in renal cell carcinoma, and correlate it with different patient clinicopathological data, emphasizing on the role of COX-2 as a prognostic factor for renal cell carcinoma and to decide which cases more likely benefit from the targeted therapy later on. Patients and Methods: The present series consisted of tissue samples obtained from 47 patients (30 patients were males and 17 were females). All the tumor samples were collected from the Pathology Department, Faculty of Medicine, Alexandria University during the period from July 2009 to November 2010. Archival paraffin-embedded renal cell carcinoma tissue samples were used to prepare tissue microarray blocks for immunohistochemical staining with COX-2 antibody. Marker expression was categorized for statistical analysis then correlated to clinicopathological variables. Results: The histological types was significantly associated with COX-2 expression, with higher expression being more common in papillary and chromophobe renal cell carcinoma, the majority of these two types were in score 1 and 2 while majority of clear cell renal cell carcinoma had score 0 and 1. Conclusion: The association of COX-2 marker was related to the histologic type of tumor; COX-2 expression study might provide prognostic information regarding tumor aggressiveness. These findings suggested a potential impact of COX-2 targeted therapy in the treatment of renal cell carcinoma with overexpressed COX-2 that needs further investigation.
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