Division of Hematology and Oncology, Memorial Health Care, Pembroke Pines, FL 33028, USA.
Division of Internal Medicine, Memorial Health Care, Pembroke Pines, FL 33028, USA.
Int J Mol Sci. 2024 Feb 6;25(4):1973. doi: 10.3390/ijms25041973.
The dysregulation of the phosphatidylinositol-3-kinase (PI3K) pathway can lead to uncontrolled cellular growth and tumorigenesis. Targeting PI3K and its downstream substrates has been shown to be effective in preclinical studies and phase III trials with the approval of several PI3K pathway inhibitors by the Food and Drug Administration (FDA) over the past decade. However, the limited clinical efficacy of these inhibitors, intolerable toxicities, and acquired resistances limit the clinical application of PI3K inhibitors. This review discusses the PI3K signaling pathway, alterations in the PI3K pathway causing carcinogenesis, current and novel PI3K pathway inhibitors, adverse effects, resistance mechanisms, challenging issues, and future directions of PI3K pathway inhibitors.
磷酸肌醇-3-激酶(PI3K)途径的失调可导致细胞不受控制的生长和肿瘤发生。在过去十年中,食品和药物管理局(FDA)批准了几种 PI3K 途径抑制剂,临床前研究和 III 期临床试验表明靶向 PI3K 及其下游底物是有效的。然而,这些抑制剂的临床疗效有限,毒性不可耐受,以及获得性耐药性限制了 PI3K 抑制剂的临床应用。本文综述了 PI3K 信号通路、导致致癌作用的 PI3K 通路改变、目前和新型 PI3K 通路抑制剂、不良反应、耐药机制、挑战性问题以及 PI3K 通路抑制剂的未来方向。