Breast Disease Center, Cancer Center, West China Hospital, Sichuan University, Chengdu 610000, China.
Multi-Omics Laboratory of Breast Diseases, State Key Laboratory of Biotherapy, National Collaborative, Innovation Center for Biotherapy, West China Hospital, Sichuan University, Chengdu 610000, China.
Cells. 2022 Aug 12;11(16):2508. doi: 10.3390/cells11162508.
Phosphatidylinositol 3-kinase (PI3K), protein kinase B (PKB/AKT) and mechanistic target of rapamycin (mTOR) (PAM) pathways play important roles in breast tumorigenesis and confer worse prognosis in breast cancer patients. The inhibitors targeting three key nodes of these pathways, PI3K, AKT and mTOR, are continuously developed. For breast cancer patients to truly benefit from PAM pathway inhibitors, it is necessary to clarify the frequency and mechanism of abnormal alterations in the PAM pathway in different breast cancer subtypes, and further explore reliable biomarkers to identify the appropriate population for precision therapy. Some PI3K and mTOR inhibitors have been approved by regulatory authorities for the treatment of specific breast cancer patient populations, and many new-generation PI3K/mTOR inhibitors and AKT isoform inhibitors have also been shown to have good prospects for cancer therapy. This review summarizes the changes in the PAM signaling pathway in different subtypes of breast cancer, and the latest research progress about the biomarkers and clinical application of PAM-targeted inhibitors.
磷脂酰肌醇 3-激酶(PI3K)、蛋白激酶 B(PKB/AKT)和雷帕霉素靶蛋白(mTOR)(PAM)通路在乳腺癌的发生中起着重要作用,并为乳腺癌患者带来更差的预后。针对这些通路的三个关键节点(PI3K、AKT 和 mTOR)的抑制剂不断被开发。为了使乳腺癌患者真正受益于 PAM 通路抑制剂,有必要阐明 PAM 通路在不同乳腺癌亚型中的异常改变的频率和机制,并进一步探索可靠的生物标志物,以确定适合精准治疗的人群。一些 PI3K 和 mTOR 抑制剂已被监管机构批准用于治疗特定的乳腺癌患者人群,许多新一代的 PI3K/mTOR 抑制剂和 AKT 同工型抑制剂也显示出在癌症治疗方面具有良好的前景。本综述总结了 PAM 信号通路在不同亚型乳腺癌中的变化,以及 PAM 靶向抑制剂的生物标志物和临床应用的最新研究进展。