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Inhibitory effect of STAT3 gene combined with CDDP on growth of human Wilms tumour SK-NEP-1 cells

机译:STAT3基因与CDDP结合对人Wilms肿瘤SK-NEP-1细胞生长的抑制作用

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摘要

To investigate the effects of signal transducer and activator of transcription 3 (STAT3) combined with cisplatin (CDDP) on the growth of human Wilms tumour (WT) SK-NEP-1 cell subcutaneous xenografts in nude mice and the possible mechanisms. Human WT SK-NEP-1 cells were subcutaneously transplanted to establish the BALB/c nude mice xenograft model. Mice were randomly divided into five groups: blank control group, adenovirus control group (NC group), STAT3 group, CDDP group and STAT3 plus CDDP group (combination group). Tumour volume and tumour weight were observed during the therapeutic process. The expression levels of STAT3, glucose regulatory protein 78 (GRP78) and BCL2-associated X protein (BAX) were evaluated by immunohistochemical analysis. Compared with the STAT3 group or CDDP group, the tumour weight and volume was significantly reduced in the combination group (P<0.05). No statistical significance was found in NC group compared with the blank control group (P > 0.05). Immunohistochemical analysis showed that STAT3, GRP78 and BAX protein levels in the combination group were significantly higher than those in STAT3 group and CDDP group (P<0.05). Exogenous STAT3 and CDDP may synergistically inhibit the xenograft tumour growth through up-regulation of BAX protein via GRP78.
机译:研究信号转导和转录激活因子3(STAT3)与顺铂(CDDP)结合对裸鼠人Wilms肿瘤(WT)SK-NEP-1细胞皮下移植瘤生长的影响及其可能的机制。将人WT SK-NEP-1细胞皮下移植以建立BALB / c裸鼠异种移植模型。将小鼠随机分为五组:空白对照组,腺病毒对照组(NC组),STAT3组,CDDP组和STAT3加CDDP组(联合组)。在治疗过程中观察到肿瘤体积和肿瘤重量。通过免疫组化分析评估STAT3,葡萄糖调节蛋白78(GRP78)和BCL2相关X蛋白(BAX)的表达水平。与STAT3组或CDDP组相比,联合组的肿瘤重量和体积明显减少(P <0.05)。与空白对照组相比,NC组无统计学意义(P> 0.05)。免疫组化分析显示,联合组STAT3,GRP78和BAX蛋白水平明显高于STAT3组和CDDP组(P <0.05)。外源STAT3和CDDP可能通过上调BRP蛋白通过GRP78协同抑制异种移植瘤的生长。

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