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YBX1 mediates autophagy by targeting p110β and decreasing the sensitivity to cisplatin in NSCLC

机译:YBX1通过靶向P110β并降低NSCLC中顺铂的敏感性介导自噬

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Y-box binding protein 1 (YBX1) is involved in the development of multiple types of tumors. However, the relationship between YBX1 and autophagy in non-small cell lung cancer (NSCLC) remains unclear. In this study, we analyzed the expression and clinical significance of YBX1 and markers of autophagy (LC3I/II) in NSCLC and examined their roles in regulating sensitivity to cisplatin in NSCLC. The retrospective analysis of patients with NSCLC indicated that YBX1 was positively correlated with autophagy. Increased levels of YBX1 or autophagy also observed in NSCLC cells compared with those in 16HBE cells. Compared to the controls, the knockdown of YBX1 expression suppressed autophagy, increased drug sensitivity and promoted apoptosis in response to cisplatin in NSCLC cells by targeting the p110β promoter and inhibiting p110β/Vps34/beclin1 signaling pathways. We also demonstrated in an in vivo study that the overexpressed YBX1 effectively increased NSCLC growth and progression and decreased the sensitivity to cisplatin by inducing autophagy in a xenograft tumor model, and these effects were concomitant with the increasing of p110β and beclin1 expression. Collectively, these results show that YBX1 plays an essential role in autophagy in NSCLC.
机译:Y盒结合蛋白1(YBX1)参与多种肿瘤的发育。然而,在非小细胞肺癌(NSCLC)中YBX1和自噬之间的关系仍不清楚。在这项研究中,我们分析了NSCLC中YBX1和自噬(LC3I / II)的标记的表达及临床意义,并检查了其在NSCLC中对顺铂的敏感性的作用。 NSCLC患者的回顾性分析表明YBX1与自噬呈正相关。与16HBE细胞中的那些相比,在NSCLC细胞中也观察到增加的YBX1或自噬水平。与对照相比,通过靶向P110β启动子并抑制P110β/ VPS34 / BECLIN1信号通路,YBX1表达的敲低抑制了逐噬细胞,增加了药物敏感性,增加了药物敏感性,增加了药物敏感性,增加了药物敏感性,促进了Cisclatin。我们还在体内研究中证明了过表达的YBX1有效地增加了NSCLC生长和进展,并通过在异种移植肿瘤模型中诱导自噬降低了对顺铂的敏感性,并且这些效果伴随着P110β和BECLIN1表达的增加。总的来说,这些结果表明,YBX1在NSCLC中的自噬起到了重要作用。

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