Wang Andi, Zhong Hua
a Department of Hematology , South Campus Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University , Shanghai , People's Republic of China.
Hematology. 2018 Dec;23(10):729-739. doi: 10.1080/10245332.2018.1486064. Epub 2018 Jun 14.
To summarize the effects of the bone marrow niche on hematopoiesis and leukemogenesis and discuss the chemotherapy resistance that can arise from interactions between the niche and leukemia stem cells.
We review the major roles of the bone marrow niche in cell proliferation, adhesion and drug resistance. The signaling pathways and major molecular participants in the niche are discussed. We also address potential niche-targeting strategies for the treatment of acute myeloid leukemia (AML).
The bone marrow niche supports normal hematopoiesis and affects acute myeloid leukemia (AML) initiation, progression and chemotherapy resistance.
AML is a group of heterogeneous malignant diseases characterized by the excessive proliferation of hematopoietic stem and/or progenitor cells. Even with intensive chemotherapy regimens and stem cell transplantation, the overall survival rate for AML is poor. The bone marrow niches of malignant cells are remodeled into a leukemia-permissive environment, and these reformed niches protect AML cells from chemotherapy-induced cell death. Inhibiting the cellular and molecular interactions between the niche and leukemia cells is a promising direction for targeted therapies for AML treatment.
Interactions between leukemia cells and the bone marrow niche influence hematopoiesis, leukemogenesis, and chemotherapy resistance in AML and require ongoing study. Understanding the mechanisms that underlie these interactions will help identify rational niche-targeting therapies to improve treatment outcomes in AML patients.
总结骨髓微环境对造血和白血病发生的影响,并探讨微环境与白血病干细胞相互作用可能产生的化疗耐药性。
我们回顾了骨髓微环境在细胞增殖、黏附及耐药性方面的主要作用。讨论了微环境中的信号通路及主要分子参与者。我们还探讨了治疗急性髓系白血病(AML)的潜在靶向微环境策略。
骨髓微环境支持正常造血,并影响急性髓系白血病(AML)的起始、进展及化疗耐药性。
AML是一组异质性恶性疾病,其特征为造血干细胞和/或祖细胞过度增殖。即使采用强化化疗方案及干细胞移植,AML的总体生存率仍较低。恶性细胞的骨髓微环境被重塑为有利于白血病发生的环境,这些重塑的微环境保护AML细胞免受化疗诱导的细胞死亡。抑制微环境与白血病细胞之间的细胞和分子相互作用是AML靶向治疗的一个有前景的方向。
白血病细胞与骨髓微环境之间的相互作用影响AML中的造血、白血病发生及化疗耐药性,需要持续研究。了解这些相互作用的潜在机制将有助于确定合理的靶向微环境治疗方法,以改善AML患者的治疗效果。