胰腺癌
转移
癌症
MMP2型
医学
癌症研究
CA19-9号
肝癌
肿瘤科
小RNA
胰腺疾病
内科学
胰腺
生物
基因
生物化学
作者
Yi Zou,Jian Li,Zhixin Chen,Xiaogang Li,Shiying Zheng,Yi Dong,Anyuan Zhong,Jen‐Ping Chen
出处
期刊:Carcinogenesis
[Oxford University Press]
日期:2015-04-11
卷期号:36 (6): 676-684
被引量:42
标识
DOI:10.1093/carcin/bgv027
摘要
We investigated mechanisms of pancreatic cancer metastasis and defined the biological role of miR-29c in pancreatic cancer metastasis. After two rounds of cell selection in vivo, pancreatic cancer cells with various metastatic potentials derived from spontaneous liver metastases were used as a model of pancreatic cancer to determine the role of miR-29c in pancreatic cancer metastasis. Pancreatic cancer samples were analyzed for miRNA-29c expression, and these levels were associated with survival between groups. miR-29c suppresses cell migration and invasion by targeting the MMP2 3′UTR. Overexpression of miR-29c suppresses pancreatic cancer liver metastasis in a nude mouse orthotopic implantation model. miR-29c expression was associated with metastasis and pancreatic cancer patient survival. miR-29c plays an important role in mediating pancreatic cancer metastasis to the liver by targeting MMP2. Therefore, miR-29c may serve as a novel marker of pancreatic cancer metastasis and possibly as a therapeutic target to treat pancreatic cancer liver metastasis.
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