Department of Medical Oncology, Regina Elena National Cancer Institute, via Elio Chianesi 53, 00144 Rome, Italy.
Anticancer Res. 2013 Jan;33(1):21-8.
Mammalian target of rapamycin (mTOR) is a crucial mediator of tumor progression and may be a promising target in a significant proportion of patients with breast cancer. More specifically, the phosphatidylinositol-3-kinase (PI3K)/protein kinase B (AKT)/mTOR pathway plays a critical role in multiple cellular functions including metabolism, proliferation, growth and survival. This pathway is higly active in many types of cancer and is linked to resistance to many types of therapy. Direct blockade of the mTOR pathway is a new area in breast cancer therapy, with the potential to modulate growth factor- and estrogen-dependent and estrogen-independent pathways, which contribute to the pathogenesis and progression of tumors. Thus, inhibitors of mTOR are of interest as potential therapeutic agents for patients with breast cancer, everolimus and temsirolimus being the main representatives of this category. This review of the literature analyzes the available data emerging from trials and evaluates the efficacy and safety of mTOR inhibitors in all subtypes of breast cancer.
哺乳动物雷帕霉素靶蛋白(mTOR)是肿瘤进展的关键介质,可能是相当一部分乳腺癌患者有前途的治疗靶点。更具体地说,磷脂酰肌醇-3-激酶(PI3K)/蛋白激酶 B(AKT)/mTOR 途径在包括代谢、增殖、生长和存活在内的多种细胞功能中发挥关键作用。该途径在许多类型的癌症中非常活跃,并与对许多类型的治疗的耐药性有关。mTOR 途径的直接阻断是乳腺癌治疗的一个新领域,有可能调节生长因子和雌激素依赖性和雌激素非依赖性途径,这些途径有助于肿瘤的发病机制和进展。因此,mTOR 抑制剂作为乳腺癌患者的潜在治疗药物引起了关注,依维莫司和替西罗莫司是该类药物的主要代表。对文献的回顾分析了来自试验的现有数据,并评估了 mTOR 抑制剂在所有乳腺癌亚型中的疗效和安全性。