Ding Hui, Gui Xianhua, Lin Xubo, Chen Ruhua, Ma Tieliang, Sheng Yunlu, Cai Hourong, Fen Yan
1 Department of Respiratory Medicine, Yixing People's Hospital, Affiliated Jiangsu University, Yixing, Jiangsu, China.
2 Department of Respiratory Medicine, Nanjing Drum Tower Hospital, Affiliated Hospital of Nanjing University Medical School, Nanjing, Jiangsu, China.
Technol Cancer Res Treat. 2017 Oct;16(5):645-653. doi: 10.1177/1533034616670443. Epub 2016 Sep 29.
The purpose of this study was to examine the MAC30 expression in non-small cell lung cancer and to evaluate its prognostic value on therapeutic response in patients with non-small cell lung cancer receiving postoperative chemotherapy. Among a total of 218 retrospective Chinese patients with non-small cell lung cancer, 164 patients receiving adjuvant chemotherapy were enrolled in this study. Real-time polymerase chain reaction was performed to confirm the expression of MAC30 messenger RNA in 32 cases of non-small cell lung cancer tumors with the corresponding nontumor lung tissues. The MAC30 protein expression in all specimens was analyzed by immunohistochemical staining. Moreover, we assessed the correlation of MAC30 expression with clinicopathological features, therapeutic response, and survival of patients. Here, we observed the increased expression of MAC30 messenger RNA in patients with non-small cell lung cancer compared to those in control samples. The overexpression of MAC30 was strongly associated with poor tumor differentiation, high tumor-node-metastasis stage, and lymph node metastasis. In addition, we observed that patients with increased MAC30 expression showed gloomy overall survival and disease-free survival. A multivariate analysis explicated that higher MAC30 expression was a valuable independent prognostic factor of poorer tumor differentiation, shorter overall survival, and disease-free survival in patients receiving chemotherapy. MAC30 could be a useful biomarker of tumor differentiation and outcome of patients with non-small cell lung cancer. Overexpression of MAC30 predicts a worse tumor differentiated stage and prognosis in patients with non-small cell lung cancer receiving adjuvant chemotherapy.
本研究的目的是检测非小细胞肺癌中MAC30的表达,并评估其对接受术后化疗的非小细胞肺癌患者治疗反应的预后价值。在总共218例中国非小细胞肺癌回顾性患者中,164例接受辅助化疗的患者纳入本研究。采用实时聚合酶链反应检测32例非小细胞肺癌肿瘤及其相应癌旁肺组织中MAC30信使核糖核酸的表达。通过免疫组织化学染色分析所有标本中MAC30蛋白的表达。此外,我们评估了MAC30表达与患者临床病理特征、治疗反应和生存情况的相关性。在此,我们观察到与对照样本相比,非小细胞肺癌患者中MAC30信使核糖核酸的表达增加。MAC30的过表达与肿瘤低分化、高TNM分期和淋巴结转移密切相关。此外,我们观察到MAC30表达增加的患者总生存期和无病生存期较差。多因素分析表明,较高的MAC30表达是接受化疗患者肿瘤低分化、总生存期和无病生存期较差的有价值的独立预后因素。MAC30可能是预测非小细胞肺癌患者肿瘤分化和预后的有用生物标志物。MAC30的过表达预示着接受辅助化疗的非小细胞肺癌患者肿瘤分化阶段更差,预后更差。