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哺乳动物雷帕霉素靶蛋白抑制剂研发的现状和未来方向。

Current and future directions in mammalian target of rapamycin inhibitors development.

机构信息

Istituto Nazionale dei Tumori, via Venezian 1, Milan, Italy.

出版信息

Expert Opin Investig Drugs. 2011 Mar;20(3):381-94. doi: 10.1517/13543784.2011.541154. Epub 2011 Feb 8.

Abstract

INTRODUCTION

The mammalian target of the rapamycin (mTOR) signalling pathway has a central role in the regulation of cell growth, survival and angiogenesis and the frequent dysregulation of this pathway in tumor cells makes it a crucial target in the treatment of cancer. Temsirolimus and everolimus are approved for use in metastatic renal cell carcinoma and temsirolimus is also approved for mantle cell lymphoma. All three rapalogs, temsirolimus, everolimus and deforolimus, are currently being evaluated in Phase III studies in several tumors.

AREAS COVERED

This paper provides a review of the published literature on the mTOR pathway and related pathway signaling, analogs and novel mTOR inhibitors. The most recent and important data on the mTOR pathway, the role of mTOR inhibitors in cancer treatment and the current status of development of second-generation highly potent and selective mTOR inhibitors are overviewed.

EXPERT OPINION

The published data on new mTOR inhibitors are still limited, but the available preclinical results indicate that they have a potent antiproliferative activity against a broad panel of tumor cell lines, have a favorable safety profile, can obtain disease stabilization or even tumor regression and, in some cases, enhance the efficacy of other targeted or standard-of-care anticancer drugs when used in vivo in preclinical studies.

摘要

简介

哺乳动物雷帕霉素靶蛋白(mTOR)信号通路在细胞生长、存活和血管生成的调节中具有核心作用,肿瘤细胞中该通路的频繁失调使其成为癌症治疗的关键靶点。替西罗莫司和依维莫司已被批准用于转移性肾细胞癌,替西罗莫司也被批准用于套细胞淋巴瘤。所有三种雷帕霉素类似物,替西罗莫司、依维莫司和德氟罗莫司,目前都在几种肿瘤的 III 期研究中进行评估。

涵盖领域

本文综述了已发表的关于 mTOR 通路及相关通路信号、类似物和新型 mTOR 抑制剂的文献。概述了 mTOR 通路的最新和重要数据、mTOR 抑制剂在癌症治疗中的作用以及第二代高活性和选择性 mTOR 抑制剂的开发现状。

专家意见

关于新型 mTOR 抑制剂的已发表数据仍然有限,但现有临床前结果表明,它们对广泛的肿瘤细胞系具有强大的抗增殖活性,具有良好的安全性特征,可在体内获得疾病稳定甚至肿瘤消退,并且在某些情况下,在临床前研究中与其他靶向或标准治疗抗癌药物联合使用时可增强疗效。

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