Gonçalo Moniz Institute, Oswaldo Cruz Foundation (IGM-FIOCRUZ/BA), Salvador, Bahia, 40296-710, Brazil.
Gonçalo Moniz Institute, Oswaldo Cruz Foundation (IGM-FIOCRUZ/BA), Salvador, Bahia, 40296-710, Brazil.
Crit Rev Oncol Hematol. 2021 Apr;160:103277. doi: 10.1016/j.critrevonc.2021.103277. Epub 2021 Mar 11.
Acute myeloid leukemia (AML) remains the most lethal of leukemias and a small population of cells called leukemic stem cells (LSCs) has been associated with disease relapses. Some cell signaling pathways play an important role in AML survival, proliferation and self-renewal properties and are abnormally activated or suppressed in LSCs. This includes the NF-κB, Wnt/β-catenin, Hedgehog, Notch, EGFR, JAK/STAT, PI3K/AKT/mTOR, TGF/SMAD and PPAR pathways. This review aimed to discuss these pathways as molecular targets for eliminating AML LSCs. Herein, inhibitors/activators of these pathways were summarized as a potential new anti-AML therapy capable of eliminating LSCs to guide future researches. The clinical use of cell signaling pathways data can be useful to enhance the anti-AML therapy.
急性髓细胞白血病(AML)仍然是最致命的白血病,一小部分被称为白血病干细胞(LSCs)的细胞与疾病复发有关。一些细胞信号通路在 AML 的存活、增殖和自我更新特性中发挥着重要作用,并且在 LSCs 中异常激活或抑制。其中包括 NF-κB、Wnt/β-catenin、Hedgehog、Notch、EGFR、JAK/STAT、PI3K/AKT/mTOR、TGF/SMAD 和 PPAR 通路。本综述旨在讨论这些通路作为消除 AML LSCs 的分子靶点。本文总结了这些通路的抑制剂/激活剂,作为一种有潜力的新型抗 AML 疗法,能够消除 LSCs,为未来的研究提供指导。细胞信号通路数据的临床应用可能有助于增强抗 AML 治疗。