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首页> 外文期刊>Oncology letters >Tazarotene-induced gene 2 is associated with poor survival in non-small cell lung cancer
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Tazarotene-induced gene 2 is associated with poor survival in non-small cell lung cancer

机译:他扎罗汀诱导的基因2与非小细胞肺癌的不良生存相关

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摘要

The aim of the present study was to investigate the expression of tazarotene-induced gene 2 (TIG2) and evaluate the clinicopathological variables and prognostic value for non-small cell lung cancer (NSCLC) patients. Reverse transcription-polymerase chain reaction and western blotting were utilized to detect TIG2 expression in NSCLC specimens and adjacent noncancerous tissue. Furthermore, the present study investigated the protein expression and the clinicopathological significance of TIG2 in 98 paraffin-embedded NSCLC samples by using immunohistochemistry. The results of the present study demonstrated that the expression of TIG2 mRNA (P=0.003) and protein (P=0.0024) was significantly reduced in NSCLC compared with corresponding noncancerous tissue. TIG2 protein expression in NSCLC was significantly associated with lymph node metastasis (P=0.006), Tumor-Node-Metastasis stage (P=0.021) and degree of differentiation (P=0.025). The Kaplan-Meier method and log-rank test revealed that high TIG2 expression was significantly associated with increased survival of NSCLC patients (P=0.003). Multivariate analysis revealed that TIG2 expression was an independent prognostic factor of the overall survival of NSCLC patients. Decreased expression of TIG2 may be useful as a biomarker for poor prognosis in NSCLC carcinogenesis and may act as a target for gene therapy for the treatment of NSCLC patients.
机译:本研究的目的是调查他扎罗汀诱导基因2(TIG2)的表达,并评估非小细胞肺癌(NSCLC)患者的临床病理变量和预后价值。逆转录聚合酶链反应和免疫印迹被用来检测TIG2在非小细胞肺癌标本和邻近的非癌组织中的表达。此外,本研究通过免疫组化研究了98例石蜡包埋的NSCLC样品中TIG2的蛋白表达及其临床病理意义。本研究结果表明,与相应的非癌组织相比,NSCLC中TIG2 mRNA(P = 0.003)和蛋白质(P = 0.0024)的表达显着降低。非小细胞肺癌中TIG2蛋白的表达与淋巴结转移(P = 0.006),肿瘤-淋巴结转移阶段(P = 0.021)和分化程度(P = 0.025)显着相关。 Kaplan-Meier方法和对数秩检验表明,高TIG2表达与NSCLC患者的存活率增加显着相关(P = 0.003)。多变量分析显示,TIG2表达是NSCLC患者总体生存的独立预后因素。 TIG2的表达降低可作为NSCLC癌变预后不良的生物标志物,并可作为基因治疗NSCLC患者的靶标。

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