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MicroRNA-146 up-regulation predicts the prognosis of non-small cell lung cancer by miRNA in situ hybridization

机译:MicroRNA-146上调通过miRNA原位杂交预测非小细胞肺癌的预后

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Non-small cell lung cancer (NSCLC) accounts for approximately 70% of all lung cancer-related deaths worldwide. Prognostic markers are essential for the early detection of lung cancer in patients. In this study, we first identified microRNA146 (miR-146) expression in cancer cell lines using miRNA in situ hybridization (MISH) and confirmed the accuracy of MISH using q-RT-PCR. In addition, two different systems, BCIP/NBT and ELF, were used to detect the signal for a comparative analysis of the specificity of MISH. Compared to the BCIP/NBT system, the ELF detection system was more effective for MISH. Furthermore we detected the expression of miR-146 in NSCLC tissues (43 cases) and normal tissues (32 cases). Based on our results, we can conclude that miR-146 is more highly expressed in cancer tissue than normal tissue (t-test, P < 0.05) and that miR-146 can predict the prognosis of NSCLC by MISH. Our findings preliminary demonstrate that MISH can be applied as a molecular diagnostic tool to determine the expression and localization of miRNAs in cancer tissues and that miR-146, determined by MISH, predicts the prognosis of NSCLC patients.
机译:非小细胞肺癌(NSCLC)约占全球所有肺癌相关死亡的70%。预后标志物对于早期检测患者的肺癌至关重要。在这项研究中,我们首先使用miRNA原位杂交(MISH)在癌细胞系中鉴定了microRNA146(miR-146)表达,并使用q-RT-PCR证实了MISH的准确性。另外,使用了两个不同的系统BCIP / NBT和ELF来检测信号,以比较分析MISH的特异性。与BCIP / NBT系统相比,ELF检测系统对MISH更为有效。此外,我们检测到miR-146在NSCLC组织(43例)和正常组织(32例)中的表达。根据我们的结果,我们可以得出结论,miR-146在癌组织中的表达高于正常组织(t检验,P <0.05),并且miR-146可以通过MISH预测NSCLC的预后。我们的研究结果初步证明,MISH可作为分子诊断工具来确定miRNA在癌症组织中的表达和定位,并且由MISH确定的miR-146可预测NSCLC患者的预后。

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