Chatterjee Devasis, Sabo Edmond, Tavares Rosemarie, Resnick Murray B
Department of Medicine, Rhode Island Hospital, Providence, Rhode Island 02903, USA.
Clin Cancer Res. 2008 May 15;14(10):2994-3001. doi: 10.1158/1078-0432.CCR-07-4496.
Raf Kinase Inhibitory Protein (RKIP) plays a pivotal role in cancer by regulating apoptosis induced by chemotherapeutic agents, or immune-mediated stimuli and is a metastasis suppressor protein. The signal transducer and activator of transcription 3 (STAT3) is a transcription factor that is frequently activated in gastric adenocarcinomas, thereby promoting tumor growth. We examined the expression patterns of RKIP and STAT3 with regard to human gastric cancer, predicting that elevated RKIP status may favor clinical outcome.
Tissue microarrays were created from samples from 143 patients with gastric adenocarcinomas. The microarrays were immunohistochemically stained for RKIP and STAT3, and the intensity and extent of the staining was semiquantitatively scored.
In intestinal-type gastric adenocarcinomas, RKIP and STAT3, expression were inversely associated. Cytoplasmic RKIP expression directly correlated with patient survival. Nuclear STAT3 expression inversely correlated with survival. In the diffuse tumor type, no significant correlation was found between RKIP and patient outcome. In the intestinal-type gastric adenocarcinoma, multivariate analysis adjusted for treatment types revealed RKIP and tumor stage to be significant independent predictors of survival. In the diffuse tumor type, stage was the only significant predictor of survival.
These results indicate the predictive and protective role of cytoplasmic RKIP expression in gastric adenocarcinoma of the intestinal subtype. In contrast, nuclear STAT3 expression is associated with poor patient prognosis in the intestinal subtype. Significantly, we show an inverse association between RKIP and STAT3 and a positive correlation between RKIP and patient survival.
拉夫激酶抑制蛋白(RKIP)通过调节化疗药物或免疫介导刺激诱导的细胞凋亡在癌症中发挥关键作用,是一种转移抑制蛋白。信号转导和转录激活因子3(STAT3)是一种转录因子,在胃腺癌中经常被激活,从而促进肿瘤生长。我们研究了RKIP和STAT3在人类胃癌中的表达模式,预测RKIP状态升高可能有利于临床结果。
从143例胃腺癌患者的样本中制作组织微阵列。对微阵列进行RKIP和STAT3的免疫组织化学染色,并对染色强度和范围进行半定量评分。
在肠型胃腺癌中,RKIP和STAT3的表达呈负相关。细胞质RKIP表达与患者生存率直接相关。核STAT3表达与生存率呈负相关。在弥漫型肿瘤中,未发现RKIP与患者预后之间存在显著相关性。在肠型胃腺癌中,对治疗类型进行校正的多变量分析显示,RKIP和肿瘤分期是生存率的重要独立预测因素。在弥漫型肿瘤中,分期是生存率的唯一重要预测因素。
这些结果表明细胞质RKIP表达在肠型胃腺癌中具有预测和保护作用。相比之下,核STAT3表达与肠型亚型患者的不良预后相关。重要的是,我们显示RKIP与STAT3之间呈负相关,RKIP与患者生存率之间呈正相关。