The University of Texas MD Anderson Cancer Center, Department of Gastrointestinal Medical Oncology, 1515 Holcombe, Unit 426, Houston, TX 77030, USA.
Expert Opin Investig Drugs. 2012 Dec;21(12):1775-88. doi: 10.1517/13543784.2012.721353. Epub 2012 Sep 16.
Recently, deregulation of protein synthesis has begun to gain attention as a major player in cancer development and progression. Specifically, deregulation of the process of translation initiation appears to play a key role in oncogenesis. The PI3K/Akt/mTOR pathway is vital for cellular metabolism, growth and proliferation and thus an attractive therapeutic target in oncology. Accordingly, several mTOR inhibitors are currently being tested in many cancers including colorectal cancer (CRC).
In this review, the key components of the PI3K/Akt/mTOR pathways, their molecular alterations and the inhibitors targeting the mTOR pathway in CRC are described. Complex interactions with other pathways such as the MAPK pathway are analyzed, as are possible drug combinations that target this pathway. In addition, novel strategies for use of mTOR pathway inhibitors in CRC treatment are introduced.
Clinical trials of mTOR inhibitors have been investigated in CRC. mTOR inhibitors may represent an attractive antitumor target in combination with strategies to target other pathways that may overcome resistance. Further research is needed to identify critical molecular effector mechanisms, molecular markers that predict responsiveness and potential toxicities.
最近,蛋白质合成的去调控已开始作为癌症发生和发展的主要因素受到关注。具体来说,翻译起始过程的失调似乎在致癌作用中起着关键作用。PI3K/Akt/mTOR 途径对细胞代谢、生长和增殖至关重要,因此是肿瘤学中有吸引力的治疗靶点。因此,目前正在许多癌症中包括结直肠癌(CRC)中测试几种 mTOR 抑制剂。
在这篇综述中,描述了 PI3K/Akt/mTOR 途径的关键组成部分、它们的分子改变以及 CRC 中针对 mTOR 途径的抑制剂。分析了与 MAPK 途径等其他途径的复杂相互作用,以及针对该途径的可能药物组合。此外,还介绍了在 CRC 治疗中使用 mTOR 途径抑制剂的新策略。
已经在 CRC 中研究了 mTOR 抑制剂的临床试验。mTOR 抑制剂可能与靶向可能克服耐药性的其他途径的策略一起作为有吸引力的抗肿瘤靶标。需要进一步研究以确定关键的分子效应机制、预测反应性的分子标志物和潜在的毒性。