微泡
内体
小RNA
血管生成
生物标志物
癌症研究
药物输送
多发性骨髓瘤
癌症
医学
细胞生物学
生物
生物信息学
计算生物学
免疫学
纳米技术
材料科学
基因
细胞内
内科学
生物化学
作者
Aghdas Ramezani,Aida Tafazoli,Fatemeh Salimi,Mahlegha Ghavami,Hanie Arjmandi,Bahman Khalesi,Zahra Sadat Hashemi,Saeed Khalili
标识
DOI:10.1016/j.abb.2024.109994
摘要
Interactions between the plasma cells and the BM microenvironment of Multiple myeloma (MM) take place through factors such as exosomes. Many studies have confirmed the role of exosomes in these interactions. By carrying proteins, cytokines, lipids, microRNAs, etc. as their cargo, exosomes can regulate the interactions between MM plasma cells and neighboring cells and participate in the signaling between cancer cells and the environment. It has been shown that MM-derived exosomes can induce angiogenesis, enhance osteoblast activity, confer drug resistance, and have immunosuppressive properties. Abnormal cargos in endosomes originating from MM patients, can be used as a cancer biomarker to detect or screen early prognosis in MM patients. The native nanostructure of exosomes, in addition to their biocompatibility, stability, and safety, make them excellent candidates for therapeutic, drug delivery, and immunomodulatory applications against MM. On the other hand, exosomes derived from dendritic cells (DC) may be used as vaccines against MM. Thanks to the development of new 'omics' approaches, we anticipate to hear more about exosomes in fight against MM. In the present review, we described the most current knowledge on the role of exosomes in MM pathogenesis and their potential role as novel biomarkers and therapeutic tools in MM.
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