癌相关成纤维细胞
上皮-间质转换
癌症研究
生物
外体
腺样囊性癌
基因敲除
肿瘤微环境
伤口愈合
微泡
细胞生物学
癌症
免疫学
小RNA
细胞培养
转移
癌
生物化学
遗传学
肿瘤细胞
基因
作者
Hyat Ahmed Ibrahim Al-Raimi,Xiu‐Qiong Fu,Ran Yan,Lei Zhu,Jiao Li,Xue Liu,Xuesong Yang,Dongyuan Qi,Tingjiao Liu
标识
DOI:10.1016/j.arcmed.2022.12.005
摘要
Carcinoma-associated fibroblasts (CAFs) play a pivotal role in cancer progression. Salivary adenoid cystic carcinoma (SACC) has a high tendency to invade and metastasize. Understanding how CAFs interact with SACC cells is essential for developing new targeted therapies for SACC. Extracellular vesicles (EVs) play important roles in intercellular communication. However, the role of CAFs-derived EVs in SACC invasion remains poorly understood.To show that CAFs EVs are involved in the EMT of SACC and promote tumor invasion.CAFs-derived EVs were characterized by western blot and transmission electron microscopy. Wound healing and transwell assay were performed for assessing biological foundation of CAFs-EVs for tumor cells. RNA interference transfection, western blot, wound healing and transwell assay were applied to study the effect of IL6 from CAFs-EVs on SACC cells and the mechanism. A subcutaneous xenograft model was used to evaluate the EMT of SACC induced by CAFs in vivo.In this study, we show that CAFs EVs promote the migration and invasion of SACC cells. The expression of biomarkers of epithelial-mesenchymal transition (EMT) was higher in SACC cells treated with CAFs EVs than in the negative controls, and high levels of IL6 were detected in CAFs and their EVs. Knockdown of IL6 in CAFs decreased tissue invasiveness and EMT biomarker expression in SACC cells induced by CAFs EVs. CAFs EV-associated IL6 promoted SACC EMT by activating the JAK2/STAT3 signaling pathway.CAFs-derived EVs carry IL6 to improve EMT of SACC by activating the JAK2/STAT3 signaling pathway.
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