Extracellular vesicles and oncogenic signaling

被引:32
|
作者
Schubert, Antonia [1 ,2 ,3 ]
Boutros, Michael [1 ,2 ]
机构
[1] German Canc Res Ctr, Div Signaling & Funct Genom, Heidelberg, Germany
[2] Heidelberg Univ, Heidelberg, Germany
[3] Univ Med Ctr Gottingen, Clin Hematol & Med Oncol, Gottingen, Germany
关键词
exosomes; extracellular vesicles; metastasis; microvesicles; signaling; tumor progression; ENDOTHELIAL GROWTH-FACTOR; BETA-CATENIN; TUMOR-GROWTH; PROSTATE-CANCER; DENDRITIC CELLS; FACTOR RECEPTOR; EXOSOMES; EXPRESSION; VEGF; MICROVESICLES;
D O I
10.1002/1878-0261.12855
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In recent years, extracellular vesicles (EVs) emerged as potential diagnostic and prognostic markers for cancer therapy. While the field of EV research is rapidly developing and their application as vehicles for therapeutic cargo is being tested, little is still known about the exact mechanisms of signaling specificity and cargo transfer by EVs, especially in vivo. Several signaling cascades have been found to use EVs for signaling in the tumor-stroma interaction. These include potentially oncogenic, verbatim transforming, signaling cascades such as Wnt and TGF-beta signaling, and other signaling cascades that have been tightly associated with tumor progression and metastasis, such as PD-L1 and VEGF signaling. Multiple mechanisms of how these signaling cascades and EVs interplay to mediate these complex processes have been described, such as direct signal activation through pathway components on or in EVs or indirectly by influencing vesicle biogenesis, cargo sorting, or uptake dynamics. In this review, we summarize the current knowledge of EVs, their biogenesis, and our understanding of EV interactions with recipient cells with a focus on selected oncogenic and cancer-associated signaling pathways. After an in-depth look at how EVs mediate and influence signaling, we discuss potentially translatable EV functions and existing knowledge gaps.
引用
收藏
页码:3 / 26
页数:24
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