Cancer Cell Biology Research Group, School of Biomedical Sciences and Pharmacy, College of Health Medicine and Wellbeing, The University of Newcastle, Callaghan, NSW 2308, Australia.
Precision Medicine Research Program, Hunter Medical Research Institute, New Lambton Heights, NSW 2305, Australia.
Int J Mol Sci. 2022 Dec 29;24(1):563. doi: 10.3390/ijms24010563.
Acute myeloid leukaemia (AML) is a heterogeneous disease with one of the worst survival rates of all cancers. The bone marrow microenvironment is increasingly being recognised as an important mediator of AML chemoresistance and relapse, supporting leukaemia stem cell survival through interactions among stromal, haematopoietic progenitor and leukaemic cells. Traditional therapies targeting leukaemic cells have failed to improve long term survival rates, and as such, the bone marrow niche has become a promising new source of potential therapeutic targets, particularly for relapsed and refractory AML. This review briefly discusses the role of the bone marrow microenvironment in AML development and progression, and as a source of novel therapeutic targets for AML. The main focus of this review is on drugs that modulate/target this bone marrow microenvironment and have been examined in in vivo models or clinically.
急性髓系白血病 (AML) 是一种异质性疾病,其所有癌症的生存率最差。骨髓微环境越来越被认为是 AML 化疗耐药和复发的重要介质,通过基质细胞、造血祖细胞和白血病细胞之间的相互作用,支持白血病干细胞的存活。针对白血病细胞的传统疗法未能提高长期生存率,因此,骨髓龛已成为潜在治疗靶点的有前途的新来源,特别是对于复发和难治性 AML。本文简要讨论了骨髓微环境在 AML 发展和进展中的作用,以及作为 AML 新治疗靶点的来源。本篇综述的主要重点是调节/靶向该骨髓微环境的药物,并已在体内模型或临床中进行了检查。