微泡
间皮细胞
上皮-间质转换
转移
癌症研究
间皮
医学
癌症
癌细胞
病理
免疫学
生物
内科学
小RNA
生物化学
基因
作者
Guang Deng,Jinglei Qu,Ye Zhang,Xiaofang Che,Yu Cheng,Yibo Fan,Simeng Zhang,Na Di,Yunpeng Liu,Xiujuan Qu
出处
期刊:FEBS Letters
[Wiley]
日期:2017-06-23
卷期号:591 (14): 2167-2179
被引量:104
标识
DOI:10.1002/1873-3468.12722
摘要
An intact mesothelium serves as a protective barrier to inhibit peritoneal carcinomatosis. Cancer-derived exosomes can mediate directional tumor metastasis; however, little is known about whether gastric cancer-derived exosomes will destroy the mesothelial barrier and promote peritoneal dissemination. Here, we demonstrate that gastric cancer-derived exosomes facilitate peritoneal metastasis by causing mesothelial barrier disruption and peritoneal fibrosis. Injury of peritoneal mesothelial cells elicited by gastric cancer-derived exosomes is through concurrent apoptosis and mesothelial-to-mesenchymal transition (MMT). Additionally, upregulation of p-ERK in peritoneal mesothelial cells is primarily responsible for the MMT while contributing little to apoptosis. Together, these data support the concept that exosomes play a crucial role in remodeling the premetastatic microenvironment and identify a novel mechanism for peritoneal metastasis of gastric carcinoma.
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