Mendes Manuel, Monteiro Ana C, Neto Estrela, Barrias Cristina C, Sobrinho-Simões Manuel A, Duarte Delfim, Caires Hugo R
i3S-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, 4200-135 Porto, Portugal.
ICBAS-Instituto de Ciências Biomédicas de Abel Salazar, Universidade do Porto, 4050-313 Porto, Portugal.
Int J Mol Sci. 2024 Apr 17;25(8):4430. doi: 10.3390/ijms25084430.
Acute myeloid leukaemia (AML) management remains a significant challenge in oncology due to its low survival rates and high post-treatment relapse rates, mainly attributed to treatment-resistant leukaemic stem cells (LSCs) residing in bone marrow (BM) niches. This review offers an in-depth analysis of AML progression, highlighting the pivotal role of extracellular vesicles (EVs) in the dynamic remodelling of BM niche intercellular communication. We explore recent advancements elucidating the mechanisms through which EVs facilitate complex crosstalk, effectively promoting AML hallmarks and drug resistance. Adopting a temporal view, we chart the evolving landscape of EV-mediated interactions within the AML niche, underscoring the transformative potential of these insights for therapeutic intervention. Furthermore, the review discusses the emerging understanding of endothelial cell subsets' impact across BM niches in shaping AML disease progression, adding another layer of complexity to the disease progression and treatment resistance. We highlight the potential of cutting-edge methodologies, such as organ-on-chip (OoC) and single-EV analysis technologies, to provide unprecedented insights into AML-niche interactions in a human setting. Leveraging accumulated insights into AML EV signalling to reconfigure BM niches and pioneer novel approaches to decipher the EV signalling networks that fuel AML within the human context could revolutionise the development of niche-targeted therapy for leukaemia eradication.
急性髓系白血病(AML)的治疗仍然是肿瘤学中的一项重大挑战,因为其生存率低且治疗后复发率高,这主要归因于存在于骨髓(BM)微环境中的治疗抗性白血病干细胞(LSCs)。本综述对AML的进展进行了深入分析,强调了细胞外囊泡(EVs)在BM微环境细胞间通讯动态重塑中的关键作用。我们探讨了最近的进展,阐明了EVs促进复杂串扰、有效促进AML特征和耐药性的机制。从时间角度来看,我们描绘了AML微环境中EV介导相互作用的不断演变的格局,强调了这些见解对治疗干预的变革潜力。此外,该综述讨论了对内皮细胞亚群在塑造AML疾病进展过程中对整个BM微环境的影响的新认识,这为疾病进展和治疗抗性增加了另一层复杂性。我们强调了前沿方法的潜力,如芯片器官(OoC)和单EV分析技术,以在人体环境中提供对AML-微环境相互作用前所未有的见解。利用对AML EV信号传导积累的见解来重新配置BM微环境,并开创在人体环境中破译推动AML的EV信号网络的新方法,可能会彻底改变根除白血病的微环境靶向治疗的发展。