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HSP70 Inhibition Synergistically Enhances the Effects of Magnetic Fluid Hyperthermia in Ovarian Cancer

机译:HSP70抑制协同增强磁流体热疗在卵巢癌中的影响

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Hyperthermia has been investigated as a potential treatment for cancer. However, specificity in hyperthermia application remains a significant challenge. Magnetic fluid hyperthermia (MFH) may be an alternative to surpass such a challenge, but implications of MFH at the cellular level are not well understood. Therefore, the present work focused on the examination of gene expression after MFH treatment and using such information to identify target genes that wheninhibited could produce an enhanced therapeutic outcome after MFH. Genomic analyzes were performed using ovarian cancer cells exposed to MFH for 30 minutes at 43 degrees C, which revealed that heat shock protein (HSP) genes, including HSPA6, were upregulated. HSPA6 encodes the Hsp70, and its expression was confirmed by PCR in HeyA8 and A2780cp20 ovarian cancer cells. Two strategies were investigated to inhibit Hsp70-related genes, siRNA and Hsp70 protein function inhibition by 2-phenylethyenesulfonamide (PES). Both strategies resulted in decreased cell viability following exposure to MFH. Combination index was calculated for PES treatment reporting a synergistic effect. In vivo efficacy experiments with HSPA6 siRNA and MFH were performed using the A2780cp20 and HeyA8 ovarian cancer mouse models. A significantly reduction in tumor growth rate was observed with combination therapy. PES and MFH efficacy were also evaluated in the HeyA8 intraperitoneal tumor model, and resulted in robust antitumor effects. This work demonstrated that HSP70 inhibition combination with MFH generate a synergistic effect and could be a promising target to enhance MFH therapeutic outcomes in ovarian cancer. Mol Cancer Ther; (C) 2017 AACR.
机译:热疗被调查为癌症的潜在治疗。然而,高温申请的特异性仍然是一个重大挑战。磁性流体热疗(MFH)可能是超越这种挑战的替代方案,但MFH在细胞水平上的影响并不能理解。因此,目前的作品集中于MFH处理后基因表达的检查,并使用此类信息鉴定靶基因,即在MFH后可能产生增强的治疗结果。在43摄氏度下使用暴露于MFH的卵巢癌细胞进行基因组分析,揭示了较上调热休克蛋白(HSP)基因,包括HSPA6。 HSPA6编码HSP70,并通过Heya8和A2780cp20卵巢癌细胞的PCR确认其表达。研究了两种策略以抑制HSP70相关基因,siRNA和HSP70蛋白功能抑制2-苯基乙胺磺胺酰胺(PES)。在接触MFH后,两种策略导致细胞活力降低。针对PES治疗报告协同效应计算组合指数。使用HSPA6 siRNA和MFH的体内疗效实验使用A2780CP20和Heya8卵巢癌小鼠模型进行。用联合治疗观察到肿瘤生长速率显着降低。在Heya8腹膜内肿瘤模型中也评估了PES和MFH疗效,并导致抗肿瘤效果稳健。这项工作表明,HSP70抑制与MFH的抑制组合产生协同效应,并且可以是增强卵巢癌中MFH治疗结果的有希望的靶标。 mol癌症; (c)2017年AACR。

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