Rybárová Silvia, Hodorová Ingrid, Mihalik Jozef, Mirossay Ladislav
Department of Anatomy, Faculty of Medicine, P.J. Šafárik University, Šrobárova 2, 041 80 Košice, Slovak Republic.
Department of Anatomy, Faculty of Medicine, P.J. Šafárik University, Šrobárova 2, 041 80 Košice, Slovak Republic.
Acta Histochem. 2014 Oct;116(8):1390-8. doi: 10.1016/j.acthis.2014.09.002. Epub 2014 Sep 23.
We detected MRP1 (multidrug resistance-associated protein 1) and GSTp1 (glutathione-S-transferase p1) protein expression in samples of non-small cell lung cancer (NSCLC) and our results were compared to basic clinicopathological parameters. The indirect immunohistochemical method was used for localization of monitored proteins. A total of 135 tissue samples of NSCLC were characterized according to histopathological type of tumor. Next, we compared our results with basic clinicopathological parameters (histopathological type of tumor, tumor grade and TNM stage of disease). In MRP1 and GSTp1 positive tumor cells, strong brown cytoplasmic immunostaining was visible. In our set of samples 71% showed MRP1 positivity, while according to histopathological type the squamous cell carcinoma reached the highest level of positivity (76%). Our GSTp1 results showed that similarly to MRP1, 70% of samples were GSTp1 positive. According to histopathological type the adenocarcinoma samples showed the highest GSTp1 expression (77%). For precise statistical evaluation the Kruskal-Wallis, Chi-square and Mann-Whitney tests were used. We did not find any statistically significant correlations between MRP1 and clinicopathological parameters. In the group of GSTp1, by Mann-Whitney test we found a statistically significant correlation between GSTp1 and histological grade (p=0.025) in adenocarcinoma samples. As this was only one group of statistically significant correlation we wanted to confirm this finding. For this we applied also Chi-square test which revealed no statistically significant dependence (p=0.077). No statistically significant relation was seen in the coexpression of both proteins (p=0.753). Despite this, the majority of samples simultaneously expressed MRP1 and GSTp1 proteins. In conclusion, our results show that MRP1 and GSTp1 proteins represent independent prognostic features in NSCLC. Nevertheless, the clinical outcome in individual patients is often difficult to predict. Identification of the factors that characterize the resistant cases would permit immediate treatment of the patients with alternative therapeutic approaches.
我们检测了非小细胞肺癌(NSCLC)样本中多药耐药相关蛋白1(MRP1)和谷胱甘肽-S-转移酶p1(GSTp1)的蛋白表达,并将结果与基本临床病理参数进行比较。采用间接免疫组织化学方法定位所监测的蛋白。根据肿瘤的组织病理学类型对135例NSCLC组织样本进行了特征分析。接下来,我们将结果与基本临床病理参数(肿瘤组织病理学类型、肿瘤分级和疾病TNM分期)进行比较。在MRP1和GSTp1阳性肿瘤细胞中,可见强烈的棕色细胞质免疫染色。在我们的样本组中,71%显示MRP1阳性,而根据组织病理学类型,鳞状细胞癌的阳性率最高(76%)。我们的GSTp1检测结果表明,与MRP1类似,70%的样本GSTp1呈阳性。根据组织病理学类型,腺癌样本的GSTp1表达最高(77%)。为了进行精确的统计评估,使用了Kruskal-Wallis检验、卡方检验和Mann-Whitney检验。我们未发现MRP1与临床病理参数之间存在任何统计学显著相关性。在GSTp1组中,通过Mann-Whitney检验,我们发现腺癌样本中GSTp1与组织学分级之间存在统计学显著相关性(p = 0.025)。由于这只是一组具有统计学显著相关性的数据,我们想证实这一发现。为此,我们还应用了卡方检验,结果显示无统计学显著相关性(p = 0.077)。两种蛋白的共表达未见统计学显著相关性(p = 0.753)。尽管如此,大多数样本同时表达MRP1和GSTp1蛋白。总之,我们的结果表明,MRP1和GSTp1蛋白是NSCLC中独立的预后特征。然而,个体患者的临床结局往往难以预测。识别耐药病例的特征因素将有助于立即采用替代治疗方法对患者进行治疗。