帕唑帕尼
替西罗莫司
阿西替尼
索拉非尼
依维莫司
医学
肾细胞癌
癌症研究
舒尼替尼
酪氨酸激酶
PI3K/AKT/mTOR通路
靶向治疗
血管生成
肿瘤科
癌症
内科学
信号转导
生物
mTOR抑制剂的发现与发展
受体
肝细胞癌
生物化学
作者
Alexander Vozianov,A K Butenko,Klaudia Żak
出处
期刊:Likars'ka sprava / Ministerstvo okhorony zdorov'ia Ukraïny
[LLC Information and Research Center Likarska Sprava]
日期:2010-04-01
卷期号:: 3-11
摘要
Two main ways playing a cardinal role in the pathogenesis of metastatic renal cell carcinoma (mRCC) have been identified in recent years, they are following: 1) a way of the mutation of a gene suppressor VHL (Van-Hippel-Lindau), stimulating various types of tyrosine-kinases participating in the development of tumors; 2) mTOR way, where ramapycyn plays a leading role, which effect proliferation and angiogenesis of mRCC. This discovery enabled the development of a new generation of highly effective medications for target-therapy of mRCCC--tyrosine-kinases inhibitors (VEGFR-1, VEGFR-2, VEGFR-3, PDGFR-alpha/PDGFR-beta, Raf-kinases, etc.) sunitimab, sorafenib, pazopanib, axitinib, etc. and mTOR inhibitors--everolimus and temsirolimus as well as monoclonal neutralising antibody VEGF (bevasizumab). The review is devoted to the analysis of antitumor activity, patient tolerance and side effect of these preparations in the system therapy of patients with mRCC.
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