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βKlotho is identified as a target for theranostics in non-small cell lung cancer

机译:βKlotho被鉴定为非小细胞肺癌治疗靶

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Non-small cell lung cancer (NSCLC) remains a great challenge, calling for the identification of novel molecular targets with diagnostic/therapeutic value. Here, we sought to characterize the expression of βKlotho and its anti-tumor roles in NSCLC. Methods: The expression of βKlotho was examined in NSCLC cells and tissues by western blot, qRT-PCR and immunohistochemistry staining respectively. Biological roles of βKlotho were revealed by a series of functional in vitro and in vivo studies. Serum βKlotho concentrations of patients were measured using specific ELISA methods. Results: Serum βKlotho concentrations of NSCLC patients were significantly lower than the control group. Moreover, βKlotho expression was negatively associated with lymph node metastasis, overall survival and progression-free survival. Overexpression of βKlotho or exogenous βKlotho administration inhibited the proliferation and migration of NSCLC cells, accompanied by induction of apoptosis, G1 to S phase arrest, and inactivation of ERK1/2, AKT and STAT3 signaling. Furthermore, βKlotho overexpression inhibited NSCLC tumor growth in vivo . Conclusions: βKlotho serves as a novel target for theranostics in NSCLC, which has potential clinical applications in the future.
机译:非小细胞肺癌(NSCLC)仍然是一个很大的挑战,呼吁鉴定具有诊断/治疗价值的新型分子靶标。在这里,我们寻求表征βKlotho的表达及其在NSCLC中的抗肿瘤作用。方法:分别通过蛋白质印迹,QRT-PCR和免疫组织化学染色在NSCLC细胞和组织中检查βKlotho的表达。体外和体内研究的一系列功能揭示了βKlotho的生物学作用。使用特定的ELISA方法测量患者血清βKlotho浓度。结果:NSCLC患者的血清βKlotho浓度明显低于对照组。此外,βKlotho表达与淋巴结转移,整体存活和无进展生存产生了负面相关。 βKlotho或外源βKlotho给药的过度表达抑制了NSCLC细胞的增殖和迁移,伴随诱导细胞凋亡,G1至S期阻滞和ERK1 / 2,AKT和Stat3信号传导的灭活。此外,βKlotho过表达抑制体内的NSCLC肿瘤生长。结论:βKlotho作为NSCLC中的Theranostics的新靶点,在未来具有潜在的临床应用。

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