Hypoxic nasopharyngeal carcinoma‐derived exosomal miR‐455 increases vascular permeability by targeting ZO‐1 to promote metastasis

Abstract

AbstractNasopharyngeal carcinoma (NPC), the most frequent reason for treatment failure in head and neck tumors, has the greatest incidence of distant metastases. Increased vascular permeability facilitates metastasis. Exosomal microRNAs (miRNAs) have been implicated in the development of the premetastatic niche and are emerging as prospective biomarkers in cancer patients. We discovered that a higher level of miR‐455 was connected to a larger propensity for NPC metastasis based on deep sequencing and RT‐qPCR. We found that hypoxia promoted NPC exosomes release and increased miR‐455 expression in a way that was hypoxia‐inducible factor 1‐alpha (HIF‐1α) dependent. Exosomes from NPC cells with high levels of miR‐455 were found to specifically target zonula occludens 1 (ZO‐1), increasing the permeability of endothelial monolayers in vitro vascular permeability and transendothelial invasion experiments. Additional in vivo studies showed that zebrafish with sustained miR‐455‐overexpressing NPC cell xenografts displayed increased tumor cell mass throughout the body. In vivo, zebrafish vascular tight junction integrity was disrupted by exosomes produced by NPC cells with elevated miR‐455 expression. Mice‐bearing xenografts further supported the finding that exosomes containing miR‐455 might reduce ZO‐1 expression in addition to promote NPC cell growth. These findings suggest that in a hypoxic microenvironment, exosomal miR‐455 released by NPC cells enhances vascular permeability and promotes metastasis by targeting ZO‐1. The HIF‐1α‐miR‐455‐ZO‐1 signaling pathway may be a promising predictor and potential therapeutic target for NPC with metastasis.