College of Life Science and Bioengineering, Beijing Jiaotong University, Beijing 100044, China.
Int J Mol Sci. 2019 Feb 11;20(3):755. doi: 10.3390/ijms20030755.
The mammalian or mechanistic target of rapamycin (mTOR) pathway plays a crucial role in regulation of cell survival, metabolism, growth and protein synthesis in response to upstream signals in both normal physiological and pathological conditions, especially in cancer. Aberrant mTOR signaling resulting from genetic alterations from different levels of the signal cascade is commonly observed in various types of cancers. Upon hyperactivation, mTOR signaling promotes cell proliferation and metabolism that contribute to tumor initiation and progression. In addition, mTOR also negatively regulates autophagy via different ways. We discuss mTOR signaling and its key upstream and downstream factors, the specific genetic changes in the mTOR pathway and the inhibitors of mTOR applied as therapeutic strategies in eight solid tumors. Although monotherapy and combination therapy with mTOR inhibitors have been extensively applied in preclinical and clinical trials in various cancer types, innovative therapies with better efficacy and less drug resistance are still in great need, and new biomarkers and deep sequencing technologies will facilitate these mTOR targeting drugs benefit the cancer patients in personalized therapy.
哺乳动物雷帕霉素靶蛋白(mTOR)途径在正常生理和病理条件下,对上游信号做出反应,对细胞存活、代谢、生长和蛋白质合成进行调控,发挥着关键作用,尤其在癌症中更是如此。不同信号级联水平的遗传改变导致异常的 mTOR 信号,在各种类型的癌症中都很常见。mTOR 信号过度激活后,促进细胞增殖和代谢,从而促进肿瘤的发生和发展。此外,mTOR 还通过不同的方式负调控自噬。我们讨论了 mTOR 信号及其关键的上游和下游因子、mTOR 通路中的特定遗传变化,以及作为治疗策略的 mTOR 抑制剂在八种实体瘤中的应用。尽管 mTOR 抑制剂的单药治疗和联合治疗已在多种癌症类型的临床前和临床试验中广泛应用,但仍需要更有效的、耐药性更低的创新疗法,新的生物标志物和深度测序技术将有助于这些 mTOR 靶向药物使癌症患者在个性化治疗中受益。