Li Jin F, Chu Yi W, Wang Guo M, Zhu Tong Y, Rong Rui M, Hou Jun, Xu Ming
Department of Urology, Zhong Shan Hospital, Shanghai Medical College, Fudan University, Shanghai, China.
BJU Int. 2009 Feb;103(3):399-405. doi: 10.1111/j.1464-410X.2008.08151.x. Epub 2008 Nov 19.
To investigate the prognostic value of regulatory T cells (Tregs) and its correlation with cyclooxygenase-2 (COX-2) expression in clear cell renal cell carcinoma (RCC).
CD4+, Foxp3+ tumour-infiltrating lymphocytes and tumour COX-2 expression were assessed by immunohistochemistry in tissue microarrays containing RCC from 125 patients. Prognostic effects of low and high expression were evaluated by Cox regression and Kaplan-Meier analysis using the median values as thresholds. The expression of Tregs and COX-2 were compared with the clinicopathological variables. In addition, Tregs and its correlation with COX-2 expression was also analysed.
Peritumoral Tregs were positively correlated with intratumoral COX-2 expression (Spearman rank correlation 0.336, P < 0.001). Peritumoral Tregs were associated with TNM stage (P = 0.001) and tumour size (P = 0.002), while intratumoral COX-2 expression was associated with TNM stage (P = 0.018) and grade (P = 0.013). Using multivariate analysis, increased peritumoral Tregs, higher TNM stage (III + IV), larger tumour size (> or =7 cm) and higher nuclear grade (III + IV) were independent predictors for significantly shorter overall survival and disease-free survival.
Increased peritumoral Tregs are associated with worse prognosis in clear cell RCC. The high intratumoral COX-2 expression may be the underlying reason for the aberrant gathering of Tregs. These results suggest that clinical application of COX-2 inhibitors may benefit those patients with higher intratumoral COX-2 immunostaining by reducing the transformation of Tregs in RCC.
探讨调节性T细胞(Tregs)在透明细胞肾细胞癌(RCC)中的预后价值及其与环氧合酶-2(COX-2)表达的相关性。
采用免疫组织化学方法,对125例RCC患者的组织芯片中的CD4+、Foxp3+肿瘤浸润淋巴细胞及肿瘤COX-2表达进行评估。以中位数为阈值,通过Cox回归和Kaplan-Meier分析评估低表达和高表达的预后影响。将Tregs和COX-2的表达与临床病理变量进行比较。此外,还分析了Tregs及其与COX-2表达的相关性。
瘤周Tregs与瘤内COX-2表达呈正相关(Spearman等级相关系数为0.336, P < 0.001)。瘤周Tregs与TNM分期(P = 0.001)和肿瘤大小(P = 0.002)相关,而瘤内COX-2表达与TNM分期(P = 0.018)和分级(P = 0.013)相关。多因素分析显示,瘤周Tregs增加、TNM分期较高(III + IV期)、肿瘤较大(≥7 cm)及核分级较高(III + IV级)是总生存期和无病生存期显著缩短的独立预测因素。
瘤周Tregs增加与透明细胞RCC的预后较差相关。瘤内COX-2高表达可能是Tregs异常聚集的潜在原因。这些结果表明,COX-2抑制剂的临床应用可能通过减少RCC中Tregs 的转化,使那些瘤内COX-2免疫染色较高的患者受益。