Increasing evidence indicates that extracellular vesicle (EV) play an important role in cancer cell-to-cell communication. The Epstein-Barr virus (EBV) encoded latent membrane protein 1 (LMP1), which is closely associated with… Click to show full abstract
Increasing evidence indicates that extracellular vesicle (EV) play an important role in cancer cell-to-cell communication. The Epstein-Barr virus (EBV) encoded latent membrane protein 1 (LMP1), which is closely associated with nasopharyngeal carcinoma (NPC) pathogenesis, can trigger multiple cell signaling pathways that affect cell progression. Several reports have shown that LMP1 promotes EV secretion, and LMP1 trafficking by EVs can enhances cancer progression and metastasis. However, the molecular mechanism by which LMP1 promotes EV secretion is not well understood. In the present study, we found that LMP1 promotes EV secretion via upregulated syndecan-2 (SDC2) and synaptotagmin-like-4 (SYTL4) through NF-κB signaling in NPC cells. Further study indicated that SDC2 interacted with syntenin, which promoted the formation of the EVs, and SYTL4 is associated with the release of EVs. Moreover, we found that stimulation of EV secretion by LMP1 can enhance the proliferation and invasion ability of recipient NPC cells and tumor growth in vivo. In summary, we found a new mechanism by which LMP1 upregulates the SDC2 and SYTL4 via NF-kB signaling to promote EV secretion, and further enhance cancer progression of NPC.
               
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