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Clinical implications of insulin-like growth factor II mRNA-binding protein 3 expression in non-small cell lung carcinoma

机译:胰岛素样生长因子ⅡmRNA结合蛋白3在非小细胞肺癌中的表达

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In order to examine the role of insulin-like growth factor II mRNA-binding protein 3 (IMP3) expression for the prognostic evaluation of non-small cell lung carcinoma (NSCLC), a total of 186 breast cancer patients, with adjacent non-tumor lung tissues, were selected for immunohistochemical staining of IMP3 protein. The NSCLC tissues and paired adjacent non-tumor tissues of six patients were quantified using reverse transcription quantitative polymerase chain reaction. The correlations between IMP3 overexpression and the clinical features of NSCLC were evaluated using the (2) test and Fisher's exact test. The survival rate was calculated using the Kaplan-Meier method, and the association between prognostic factors and patient survival was also analyzed by Cox's proportional hazards models. The results showed that IMP3 protein exhibited a mainly cytoplasmic staining pattern in the NSCLC tissues. The positive rate of IMP3 protein expression was 74.7% (139/186) in the NSCLC tissues and was significantly higher than the rate of 19.9% (37/186) in the adjacent non-tumor tissues. The expression rate of the NQO1 protein was correlated with a large tumor size, poor differentiation, lymph node metastasis, late clinical stage, and disease-free and overall survival rates in the NSCLC patients. In the early- and late-stage NSCLC groups, the disease-free and overall survival rates of the patients with IMP3 expression were significantly lower than those of the patients without IMP3 expression. Further analysis using Cox's proportional hazard regression model revealed that IMP3 expression was a significant independent hazard factor for the overall survival rate of patients with NSCLC. In conclusion, the present study found that IMP3 plays a significant role in the progression of NSCLC, and that it may potentially be used as an independent biomarker for prognostic evaluation of the cancer.
机译:为了检查胰岛素样生长因子II mRNA结合蛋白3(IMP3)的表达在非小细胞肺癌(NSCLC)预后评估中的作用,共有186例乳腺癌患者,伴有非肿瘤选择肺组织用于IMP3蛋白的免疫组织化学染色。使用逆转录定量聚合酶链反应对6例患者的NSCLC组织和配对的相邻非肿瘤组织进行了定量。使用(2)检验和Fisher精确检验评估IMP3过表达与NSCLC临床特征之间的相关性。使用Kaplan-Meier方法计算生存率,并通过Cox比例风险模型分析预后因素与患者生存之间的关联。结果表明,IMP3蛋白在NSCLC组织中主要表现为细胞质染色。在非小细胞肺癌组织中,IMP3蛋白表达的阳性率为74.7%(139/186),显着高于在相邻的非肿瘤组织中的19.9%(37/186)。 NQO1蛋白的表达率与NSCLC患者的肿瘤大,分化差,淋巴结转移,临床晚期以及无病生存率和总生存率相关。在早期和晚期NSCLC组中,具有IMP3表达的患者的无病生存率和总生存率显着低于不具有IMP3表达的患者。使用Cox比例风险回归模型进行的进一步分析表明,IMP3表达是NSCLC患者总体生存率的重要独立危险因素。总而言之,本研究发现IMP3在NSCLC的进展中起着重要作用,并且有可能被潜在地用作癌症预后评估的独立生物标志物。

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