微泡
下调和上调
结直肠癌
小RNA
转移
癌症研究
外体
肝细胞生长因子
肿瘤进展
癌症
医学
生物
内科学
基因
生物化学
受体
作者
Fei Tian,Peiyun Wang,Dan Lin,Jiajia Dai,Qibing Liu,Yu Guan,Zhan Yang,Yichen Yang,Wenpeng Wang,Jiefu Wang,Jia Liu,Lei Zheng,Yan Zhuang,Jun Hu,Junfeng Wang,Dalu Kong,Kegan Zhu
出处
期刊:Cancer Science
[Wiley]
日期:2021-07-07
卷期号:112 (9): 3744-3755
被引量:30
摘要
Abstract MicroRNAs (miRNAs) are involved in the progression of many cancers through largely unelucidated mechanisms. The results of our present study identified a gene cluster, miR‐221/222, that is constitutively upregulated in serum exosome samples of patients with colorectal carcinoma (CRC) with liver metastasis (LM); this upregulation predicts a poor overall survival rate. Using an in vitro cell coculture model, we demonstrated that CRC exosomes harboring miR‐221/222 activate liver hepatocyte growth factor (HGF) by suppressing SPINT1 expression. Importantly, miR‐221/222 plays a key role in forming a favorable premetastatic niche (PMN) that leads to the aggressive nature of CRC, which was further shown through in vivo studies. Overall, our results show that exosomal miR‐221/222 promotes CRC progression and may serve as a novel prognostic marker and therapeutic target for CRC with LM.
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