3rd Department of Breast Cancer, China Tianjin Breast Cancer Prevention, Treatment and Research center, Tianjin Medical University Institute and Hospital, Tianjin 300060, PR China.
Curr Cancer Drug Targets. 2013 Feb;13(2):175-87. doi: 10.2174/1568009611313020007.
The PI3K/Akt/mTOR signaling pathway is involved in the inhibition of tumor cell apoptosis, the promotion of cell survival, cell cycle regulation, tumor angiogenesis, invasion, and metastasis and therefore plays an important role intumorigenesis, tumor growth, patient prognosis, and tumor treatment. Recent studies have identified this signaling pathway in breast cancer, and the PI3K/Akt/mTOR pathway is therefore being considered as a new therapeutic target anda hotspot in breast cancer research. Pre-clinical studies have confirmed that PI3K inhibitors and mTOR inhibitors achieve anticancer effects by targeting different levels of the PI3K/Akt/mTOR signaling pathway. Among the PI3K inhibitors, some molecules target only PI3K, whereas others target both PI3K and mTOR. Currently, researchers tend to focus on molecular targets based on the different PI3K subtypes to achieve more targeted and specific inhibition of the PI3K pathway. However, the clinical efficacy and efficiency of these inhibitors need to be further studied. The mTOR inhibitors target mTORC1 and have become relatively well-developed targeted therapies for the PI3K/AKT/mTOR pathway. Rapamycin derivatives have been studied in Phase II / III clinical trials in breast cancer, and these derivatives achieved positive results in the treatment of metastatic breast cancer when combined with endocrine therapy or HER2-targeted therapies. This review summarizes the activation of the PI3K/AKT/mTOR pathway, its role in breast cancer, and the latest clinical trials of a variety of PI3K and mTOR inhibitors to improve the understanding of the role of these drugs in breast cancer treatment.
PI3K/Akt/mTOR 信号通路参与抑制肿瘤细胞凋亡、促进细胞存活、细胞周期调控、肿瘤血管生成、侵袭和转移,因此在肿瘤发生、肿瘤生长、患者预后和肿瘤治疗中起着重要作用。最近的研究已经确定了该信号通路在乳腺癌中的作用,因此 PI3K/Akt/mTOR 通路被认为是乳腺癌研究中的一个新的治疗靶点和热点。临床前研究已经证实,PI3K 抑制剂和 mTOR 抑制剂通过靶向 PI3K/Akt/mTOR 信号通路的不同水平来发挥抗癌作用。在 PI3K 抑制剂中,有些分子仅靶向 PI3K,而有些则同时靶向 PI3K 和 mTOR。目前,研究人员倾向于根据不同的 PI3K 亚型关注分子靶点,以实现对 PI3K 通路更有针对性和特异性的抑制。然而,这些抑制剂的临床疗效和效率仍需进一步研究。mTOR 抑制剂靶向 mTORC1,已成为 PI3K/AKT/mTOR 通路相对成熟的靶向治疗方法。雷帕霉素衍生物已在乳腺癌的 II 期/III 期临床试验中进行了研究,这些衍生物在与内分泌治疗或 HER2 靶向治疗联合治疗转移性乳腺癌时取得了积极的结果。本综述总结了 PI3K/AKT/mTOR 通路的激活及其在乳腺癌中的作用,以及各种 PI3K 和 mTOR 抑制剂的最新临床试验结果,以提高对这些药物在乳腺癌治疗中的作用的认识。