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GSK-3 抑制体外和体内增强索拉非尼在肾细胞癌 (RCC)中的抗肿瘤作用。

GSK-3 inhibition in vitro and in vivo enhances antitumor effect of sorafenib in renal cell carcinoma (RCC).

机构信息

Laboratory of Molecular Oncology, Department of Urology, Yamagata University School of Medicine, Iida-nishi 2-2-2, Yamagata 990-9585, Japan.

出版信息

Biochem Biophys Res Commun. 2012 Jul 6;423(3):490-5. doi: 10.1016/j.bbrc.2012.05.147. Epub 2012 Jun 5.

Abstract

Sorafenib is a multikinase inhibitor approved for the systemic treatment of renal cell carcinoma (RCC). However, sorafenib treatment has a limited effect due to acquired chemoresistance of RCC. Previously, we identified glycogen synthase kinase-3 (GSK-3) as a new therapeutic target in RCC. Here, we observed that sorafenib inhibits proliferation and survival of RCC cells. Significantly, we revealed that sorafenib enhances GSK-3 activity in RCC cells, which could be a potential mechanism of acquired chemoresistance. We found that pharmacological inhibition of GSK-3 potentiates sorafenib antitumor effect in vitro and in vivo. Our results suggest that combining GSK-3 inhibitor and sorafenib might be a potential new therapeutic approach for RCC treatment.

摘要

索拉非尼是一种多激酶抑制剂,被批准用于肾细胞癌(RCC)的系统治疗。然而,由于 RCC 的获得性化疗耐药性,索拉非尼的治疗效果有限。先前,我们发现糖原合酶激酶-3(GSK-3)是 RCC 的一个新的治疗靶点。在这里,我们观察到索拉非尼抑制 RCC 细胞的增殖和存活。重要的是,我们揭示了索拉非尼增强了 RCC 细胞中的 GSK-3 活性,这可能是获得性化疗耐药的潜在机制。我们发现,GSK-3 的药理学抑制增强了索拉非尼在体外和体内的抗肿瘤作用。我们的研究结果表明,GSK-3 抑制剂与索拉非尼联合应用可能是 RCC 治疗的一种潜在新的治疗方法。

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