Department of Thoracic Surgery, Daping Hospital, Third Military Medical University, Chongqing, China.
PLoS One. 2011;6(11):e24855. doi: 10.1371/journal.pone.0024855. Epub 2011 Nov 10.
In this study, we investigated whether PKR protein expression is correlated with mRNA levels and also evaluated molecular biomarkers that are associated with PKR, such as phosphorylated PKR (p-PKR) and phosphorylated eIF2α (p-eIF2α).
We determined the levels of PKR protein expression and mRNA in 36 fresh primary lung tumor tissues by using Western blot analysis and real-time reverse-transcriptase PCR (RT-PCR), respectively. We used tissue microarrays for immunohistochemical evaluation of the expression of p-PKR and p-eIF2α proteins. We demonstrated that PKR mRNA levels are significantly correlated with PKR protein levels (Spearman's rho = 0.55, p<0.001), suggesting that PKR protein levels in tumor samples are regulated by PKR mRNA. We also observed that the patients with high p-PKR or p-eIF2α expression had a significantly longer median survival than those with little or no p-PKR or p-eIF2α expression (p = 0.03 and p = 0.032, respectively). We further evaluated the prognostic effect of combined expression of p-PKR plus PKR and p-eIF2α plus PKR and found that both combinations were strong independent prognostic markers for overall patient survival on stage I and all stage patients.
Our findings suggest that PKR protein expression may controlled by transcription level. Combined expression levels of PKR and p-PKR or p-eIF2α can be new markers for predicting the prognosis of patients with NSCLC.
在这项研究中,我们研究了 PKR 蛋白表达是否与 mRNA 水平相关,并评估了与 PKR 相关的分子生物标志物,如磷酸化 PKR(p-PKR)和磷酸化 eIF2α(p-eIF2α)。
我们通过 Western blot 分析和实时逆转录 PCR(RT-PCR)分别确定了 36 例新鲜原发性肺肿瘤组织中 PKR 蛋白表达和 mRNA 的水平。我们使用组织微阵列进行 p-PKR 和 p-eIF2α 蛋白表达的免疫组织化学评估。我们证明 PKR mRNA 水平与 PKR 蛋白水平显著相关(Spearman's rho=0.55,p<0.001),提示肿瘤样本中 PKR 蛋白水平受 PKR mRNA 调节。我们还观察到,高表达 p-PKR 或 p-eIF2α 的患者中位生存时间明显长于低表达或无表达 p-PKR 或 p-eIF2α 的患者(p=0.03 和 p=0.032,分别)。我们进一步评估了 p-PKR 加 PKR 与 p-eIF2α 加 PKR 联合表达的预后效应,发现这两种组合均为 I 期和所有分期患者总生存的强独立预后标志物。
我们的研究结果表明,PKR 蛋白表达可能受转录水平调控。PKR 和 p-PKR 或 p-eIF2α 的联合表达水平可能成为预测 NSCLC 患者预后的新标志物。