Departamento de Bioquímica, Instituto de Química, Universidade de São Paulo, São Paulo, Brazil.
Urology. 2013 Oct;82(4):974.e1-7. doi: 10.1016/j.urology.2013.06.026. Epub 2013 Aug 3.
To investigate the expression of CASP7 protein in renal cell carcinoma clear cell subtype (ccRCC) and its value to predict cancer-specific survival (CSS).
A tissue microarray containing 120 samples of ccRCC, 45 non-ccRCC, and 66 nontumor paired samples from patients who underwent partial or radical nephrectomy was hybridized with anti-CASP7 antibody. Tissue sections were scored according to intensity and the percentage of stained cells. CASP7 immunostaining scores were used to estimate the association with clinicopathologic parameters and calculate Kaplan-Meier survival curves.
Reduced CASP7 expression was observed in ccRCC and non-ccRCC subtypes in comparison with nontumor renal tissues (P <.0001). CASP7 immunostaining was associated (P <.05) with clinicopathologic parameters (size, incidental tumor, clinical stage, renal vein invasion, and tumor necrosis) and correlated with CSS (P = .032) and global survival (P = .046) of patients with ccRCC. In addition, CASP7 expression was able to substratify patients with ccRCC with favorable prognosis according to low clinical stage, in which negative CASP7 staining was associated with patients with lower CSS (P = .045). Finally, CASP7 staining was able to provide significant stratification according to CSS (P = .018) among patients with ccRCC with disease relapse.
Our results implicate the loss of CASP7 expression in the aggressiveness of ccRCC and indicate its potential use as a clinical prognostic marker of the disease.
研究胱天蛋白酶 7(CASP7)蛋白在肾透明细胞癌(ccRCC)中的表达及其对预测癌症特异性生存(CSS)的价值。
采用组织微阵列技术,对 120 例 ccRCC 患者、45 例非 ccRCC 患者和 66 例接受部分或根治性肾切除术的非肿瘤配对患者的组织样本进行杂交,用抗 CASP7 抗体进行染色。根据染色细胞的强度和百分比对组织切片进行评分。使用 CASP7 免疫组化评分来评估与临床病理参数的相关性,并计算 Kaplan-Meier 生存曲线。
与非肿瘤肾组织相比,ccRCC 和非 ccRCC 亚型中观察到 CASP7 表达降低(P<.0001)。CASP7 免疫染色与临床病理参数(大小、偶然肿瘤、临床分期、肾静脉侵犯和肿瘤坏死)相关(P<.05),并与 ccRCC 患者的 CSS(P=.032)和总体生存(P=.046)相关。此外,根据低临床分期,CASP7 表达能够对 ccRCC 患者进行亚组分层,其中阴性 CASP7 染色与 CSS 较低的患者相关(P=.045)。最后,CASP7 染色能够根据 CSS 对 ccRCC 患者的疾病复发进行显著分层(P=.018)。
我们的结果表明,CASP7 表达缺失与 ccRCC 的侵袭性有关,并提示其可能作为该疾病的临床预后标志物。