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首页> 外文期刊>Journal of Thoracic Disease >Serum β-klotho is a potential biomarker in the prediction of clinical outcomes among patients with NSCLC
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Serum β-klotho is a potential biomarker in the prediction of clinical outcomes among patients with NSCLC

机译:血清β-klotho是一种潜在的生物标志物,其在NSCLC患者中预测临床结果

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Background: We aimed to investigate the β-klotho (KLB) expression in non-small cell lung cancer (NSCLC) and to determine its value as a novel molecular target for survival prognosis in patients with NSCLC. Methods: The serum KLB concentrations in 50 patients with NSCLC and the 20 healthy persons were measured by enzyme-linked immunosorbent assay (ELISA) methods. The relationship between serum KLB level, including the level change after therapy, and the progression-free survival (PFS) and overall survival (OS) were analyzed. The KLB expression in A549 cells was measured by real-time polymerase chain reaction (RT-PCR) and western blotting. The function of cells was revealed by in vitro studies. Results: The concentrations of serum KLB in patients with NSCLC were obviously lower than those in healthy subjects. KLB expression was significantly increased in patients after chemotherapy and epidermal growth factor receptor tyrosine kinase inhibitor (EGFR-TKI) targeted therapy. In addition, expression of KLB was positively related with PFS and OS. Compared with 16-human bronchial epithelial (HBE) cells, the expression level of KLB was significantly decreased in A549 cells. Overexpression of KLB suppressed the proliferation of A549 cells, along with G1-to-S phase arrest and apoptosis induction. Conclusions: KLB plays an anti-tumorigenic role in NSCLC. KLB may be a candidate target for the diagnosis and treatment of NSCLC and may serve a potentially significant role in future clinical applications.
机译:背景:我们旨在研究非小细胞肺癌(NSCLC)中的β-Klotho(KLB)表达,并确定其作为NSCLC患者患者存活预后的新分子靶标的价值。方法:通过酶联免疫吸附测定(ELISA)方法测量50例NSCLC和20名健康人患者中的血清KLB浓度。分析了血清KLB水平之间的关系,包括治疗后的水平变化以及无进展生存(PFS)和总存活(OS)。通过实时聚合酶链反应(RT-PCR)和Western印迹测量A549细胞中的KLB表达。通过体外研究揭示了细胞的功能。结果:NSCLC患者血清KLB的浓度明显低于健康受试者的浓度。化疗和表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKI)靶向治疗后患者KLB表达显着增加。此外,KLB的表达与PFS和OS呈正相关。与16人支气管上皮(HBE)细胞相比,A549细胞中KLB的表达水平显着降低。 KLB的过度表达抑制了A549细胞的增殖,以及G1至S期阻滞和凋亡诱导。结论:KLB在NSCLC中发挥抗致致瘤的作用。 KLB可以是NSCLC诊断和治疗的候选目标,并且可以在未来的临床应用中发挥潜在的重要作用。

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