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Expression and clinicopathological significance of miR-193a-3p and its potential target astrocyte elevated gene-1 in non-small lung cancer tissues

机译:miR-193a-3p及其潜在靶星形胶质细胞升高基因-1在非小肺癌组织中的表达及临床病理学意义

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Background Aberrant expression of miR-193a-3p and astrocyte elevated gene-1 (AEG-1) have been revealed to be related to the tumorigenesis of various cancers, including non-small cell lung cancer (NSCLC). However, the significance of miR-193a-3p and its correlation with AEG-1 in NSCLC has not been explored. The purpose of this study was to evaluate the association between miR-193a-3p and AEG-1 and their relationship with the clinicopathological features in NSCLC patients. Methods Via online in silico prediction, complementary sequences were found between miR-193a-3p and the 3′-untranslated region of AEG-1. Three independent cohorts were applied in the current study. Firstly, miR-193a-3p level was detected in 125 cases of NSCLC with quantitative real-time PCR (qRT-PCR). Secondly, AEG-1 protein level was evaluated in 339 cases of lung cancers with immunohistochemistry. Finally, the relationship between miR-193a-3p and AEG-1 protein expression was verified in another group with 65 cases of NSCLC. Results The results showed that miR-193a-3p level was decreased in NSCLC tissues and significantly negatively related to tumor size (r?=??0.277, P?=?0.002), clinical TNM stage (r?=??0.226, P?=?0.011), lymph node metastasis (r?=??0.186, P?=?0.038), epidermal growth factor receptor (EGFR) protein level (r?=??0.272, P?=?0.041). On the contrary, AEG-1 protein expression was up-regulated in NSCLC and positively relative to tumor size (r?=?0.240, P? Conclusion In conclusion, miR-193a-3p and AEG-1 might be responsible for the carcinogenesis and aggressiveness of NSCLC. AEG-1 has the potential to be one of the targeted genes of miR-193a-3p. However, future in vitro and in vivo experiments are needed to verify this hypothesis.
机译:背景技术MIR-193A-3P和星形胶质细胞升高的基因-1(AEG-1)的异常表达与各种癌症的肿瘤鉴定有关,包括非小细胞肺癌(NSCLC)。然而,未探讨MIR-193A-3P的重要性及其与NSCLC中AEG-1的相关性。本研究的目的是评估miR-193a-3p和aeg-1之间的关联及其与NSCLC患者临床病理特征的关系。方法通过在线在线预测,在MIR-193A-3P和AEG-1的3'-未翻译区域之间发现互补序列。在目前的研究中应用了三个独立的队列。首先,在NSCLC的125例具有定量实时PCR(QRT-PCR)中检测miR-193a-3p水平。其次,在339例具有免疫组化的肺癌病例中评价AEG-1蛋白质水平。最后,在另一组中验证了MiR-193A-3P和AEG-1蛋白表达的关系,其中NSCLC 65例。结果结果表明,NSCLC组织中的miR-193a-3p水平降低,与肿瘤大小显着呈负相关(r?= 0.277,p?= 0.002),临床TNM阶段(R?= ?? 0.226,p ?=?0.011),淋巴结转移(r?=Δ= 0.186,p?= 0.038),表皮生长因子受体(EGFR)蛋白质水平(R?= 0.272,p?= 0.041)。相反,AEG-1蛋白表达在NSCLC中升高,相对于肿瘤大小呈正常调节(R?= 0.240,P?结论,MIR-193A-3P和AEG-1可能对致癌作用负责NSCLC的侵略性。AEG-1具有MIR-193A-3P的靶向基因的潜力。然而,需要在体外​​和体内实验中的未来进行验证这一假设。

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