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甲羟戊酸途径阻断增强雷帕霉素靶蛋白激活在肾细胞癌中 mTOR 抑制剂的疗效。

Mevalonate pathway blockage enhances the efficacy of mTOR inhibitors with the activation of retinoblastoma protein in renal cell carcinoma.

机构信息

Department of Molecular-targeting Cancer Prevention, Kyoto Prefectural University of Medicine, Kawaramachi-Hirokoji, Kamigyo-ku, Kyoto, 602-8566, Japan; Department of Urology, Kyoto Prefectural University of Medicine, Japan.

Department of Molecular-targeting Cancer Prevention, Kyoto Prefectural University of Medicine, Kawaramachi-Hirokoji, Kamigyo-ku, Kyoto, 602-8566, Japan.

出版信息

Cancer Lett. 2018 Sep 1;431:182-189. doi: 10.1016/j.canlet.2018.05.025. Epub 2018 May 17.

Abstract

Renal cell carcinoma (RCC) is the most common malignancy of kidney and remains largely intractable once it recurs after resection. mTOR inhibitors have been one of the mainstays used against recurrent RCC; however, there has been a major problem of the resistance to mTOR inhibitors, and thus new combination treatments with mTOR inhibitors are required. We here retrospectively showed that regular use of antilipidemic drug statins could provide a longer progression free survival (PFS) in RCC patients prescribed with an mTOR inhibitor everolimus than without statins (median PFS, 7.5 months vs. 3.2 months, respectively; hazard ratio, 0.52; 95% CI, 0.22-1.11). In order to give a rationale for this finding, we used RCC cell lines and showed the combinatorial effects of an mTOR inhibitor with statins induced a robust activation of retinoblastoma protein, whose mechanisms were involved in statins-mediated hindrance of KRAS or Rac1 protein prenylation. Finally, statins treatment also enhanced the efficacy of an mTOR inhibitor in RCC xenograft models. Thus, we provide molecular and (pre)clinical data showing that statins use could be a drug repositioning for RCC patients to enhance the efficacy of mTOR inhibitors.

摘要

肾细胞癌 (RCC) 是肾脏最常见的恶性肿瘤,在切除后复发时仍然难以治疗。mTOR 抑制剂一直是治疗复发性 RCC 的主要药物之一;然而,mTOR 抑制剂存在严重的耐药问题,因此需要与 mTOR 抑制剂联合使用新的治疗方法。我们回顾性地发现,对于接受 mTOR 抑制剂依维莫司治疗的 RCC 患者,常规使用降脂药他汀类药物可以提供更长的无进展生存期 (PFS)(中位 PFS,7.5 个月比 3.2 个月;风险比,0.52;95%CI,0.22-1.11)。为了为这一发现提供依据,我们使用 RCC 细胞系进行研究,表明 mTOR 抑制剂与他汀类药物联合使用可强力激活视网膜母细胞瘤蛋白,其机制涉及他汀类药物介导的 KRAS 或 Rac1 蛋白异戊烯化受阻。最后,他汀类药物治疗还增强了 RCC 异种移植模型中 mTOR 抑制剂的疗效。因此,我们提供了分子和(临床前)数据,表明他汀类药物的使用可能是一种药物重新定位,可增强 RCC 患者对 mTOR 抑制剂的疗效。

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