Abstract:As key mediators of intercellular communication, exosomes play a crucial regulatory role in the pathogenesis of acute myeloid leukemia (AML) and the remodeling of the bone marrow microenvironment by participating in multiple pathological processes, including tumor angiogenesis, immune evasion, chemotherapy resistance, and functional reprogramming of stromal cells. The interactions mediated by exosomes between leukemia cells and various cellular components within the bone marrow microenvironment form a highly complex bidirectional regulatory network, profoundly influencing bone marrow microenvironment remodeling and immune homeostasis, thereby collectively promoting or suppressing AML progression. Therefore, in-depth analysis of key nodal molecules and signaling pathways within this interactive network will help clarify the pathogenesis of AML. Furthermore, it lays a solid theoretical foundation for the development of exosome-based diagnostic markers, the screening of therapeutic targets, and the formulation of combination intervention strategies, and points out a new direction for translational research.