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The Prognostic Effect of MAC30 Expression on Patients With Non–Small Cell Lung Cancer Receiving Adjuvant Chemotherapy

机译:MAC30表达对非小细胞肺癌辅助化疗患者的预后影响

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摘要

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.
机译:这项研究的目的是检查MAC30在非小细胞肺癌中的表达,并评估其对接受术后化疗的非小细胞肺癌患者的治疗反应的预后价值。在218例回顾性中国非小细胞肺癌患者中,有164例接受了辅助化疗的患者参加了这项研究。进行实时聚合酶链反应以确认MAC30信使RNA在32例非小细胞肺癌及相应的非肿瘤肺组织中的表达。通过免疫组织化学染色分析所有样品中的MAC30蛋白表达。此外,我们评估了MAC30表达与临床病理特征,治疗反应和患者生存率的相关性。在这里,我们观察到与对照组相比,非小细胞肺癌患者MAC30 Messenger RNA的表达增加。 MAC30的过表达与肿瘤分化差,肿瘤-淋巴结转移期高和淋巴结转移密切相关。此外,我们观察到具有增加的MAC30表达的患者表现出总体生存率低下和无病生存期。多变量分析表明,较高的MAC30表达是接受化疗的患者肿瘤分化较差,总生存期较短和无病生存期的重要独立预后因素。 MAC30可能是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的肿瘤分化阶段和预后更差。

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