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舒尼替尼、索拉非尼及mTOR抑制剂在肾癌中的应用

Sunitinib, sorafenib and mTOR inhibitors in renal cancer.

作者信息

Radulovic Sinisa, Bjelogrlic Snezana K

机构信息

Department of Translational Research, Institute for Oncology and Radiology of Serbia, Belgrade, Serbia.

出版信息

J BUON. 2007 Sep;12 Suppl 1:S151-62.

Abstract

Understanding the alterations in cellular protein interactions and their relations to genetic mutations that cause renal cell carcinoma (RCC) provides a unique opportunity for the development of disease-specific therapy for patients with advanced forms of this disease. There is substantial evidence of an association between mutation on von Hippel-Lindau (VHL) gene and the earliest stages of tumorigenesis of RCC. The main consequence of VHL loss is the upregulation of downstream proangiogenic factors leading to highly vascular tumors. Overexpression of hypoxia inducible factor (HIF) is also caused by the mammalian target of rapamycin (mTOR), a key component of signaling pathways inside the cell, involved in cell proliferation. The inhibition of proangiogenic factors and mTOR was the main idea behind the development of new targeted agents in advanced RCC. Since December 2005, 3 targeted agents have been approved by the U.S. Food and Drug Administration (FDA) for the treatment of advanced RCC: sorafenib, sunitinib and temsirolimus. Sorafenib and sunitinib are synthetic, orally active agents shown to directly inhibit vascular endothelial growth factor receptors -2 and -3 (VEGFR-2, VEGFR-3) and platelet-derived growth factor receptor beta (PDGFR-beta), while temsirolimus is an mTOR inhibitor. Recent clinical studies form the basis for new guidelines for the treatment of advanced RCC: sorafenib should be used as a second-line treatment, sunitinib as the first-line therapy for good and intermediate-risk patients, and temsirolimus should be considered as first-line treatment for poor-risk patients. Future approaches to targeted therapy should focus on optimizing the use of current active drugs, exploring their combinations or investigating their sequential use. In addition, it is important to define the mechanisms of resistance on their use and to further investigate biomarkers and enhance treatment efficacy for the individual patients. The development of these targeted therapies represents an exciting step forward in the treatment of advanced RCC.

摘要

了解细胞蛋白质相互作用的改变及其与导致肾细胞癌(RCC)的基因突变之间的关系,为开发针对这种疾病晚期患者的疾病特异性疗法提供了独特的机会。有大量证据表明,冯·希佩尔-林道(VHL)基因突变与RCC肿瘤发生的最早阶段之间存在关联。VHL缺失的主要后果是下游促血管生成因子上调,导致肿瘤血管高度丰富。缺氧诱导因子(HIF)的过表达也是由哺乳动物雷帕霉素靶蛋白(mTOR)引起的,mTOR是细胞内信号通路的关键组成部分,参与细胞增殖。抑制促血管生成因子和mTOR是晚期RCC新型靶向药物开发背后的主要理念。自2005年12月以来,3种靶向药物已被美国食品药品监督管理局(FDA)批准用于治疗晚期RCC:索拉非尼、舒尼替尼和替西罗莫司。索拉非尼和舒尼替尼是合成的口服活性药物,已证明可直接抑制血管内皮生长因子受体-2和-3(VEGFR-2、VEGFR-3)以及血小板衍生生长因子受体β(PDGFR-β),而替西罗莫司是一种mTOR抑制剂。近期的临床研究为晚期RCC的新治疗指南奠定了基础:索拉非尼应用作二线治疗,舒尼替尼用作中高危患者的一线治疗,替西罗莫司应被视为低危患者的一线治疗。未来的靶向治疗方法应侧重于优化当前活性药物的使用、探索其联合使用或研究其序贯使用。此外,确定其使用过程中的耐药机制以及进一步研究生物标志物并提高个体患者的治疗效果也很重要。这些靶向治疗的发展代表了晚期RCC治疗向前迈出的令人兴奋的一步。

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