胰腺癌
转移
癌症研究
癌症
MMP2型
车站3
生物
癌细胞
分子肿瘤学
MMP9公司
医学
癌变
信号转导
内科学
下调和上调
基因
细胞生物学
遗传学
作者
Bin Hu,Kundong Zhang,Shaobo Li,Hao Li,Zhao-Wen Yan,Li Huang,Jianghong Wu,Xiao Han,Weiliang Jiang,Tunike Mulatibieke,Lin Zheng,Rong Wan,Xingpeng Wang,Guoyong Hu
出处
期刊:Cancer Letters
[Elsevier BV]
日期:2016-07-01
卷期号:376 (2): 387-398
被引量:38
标识
DOI:10.1016/j.canlet.2016.04.013
摘要
Hypermethylated in cancer 1 (HIC1) is a tumour suppressor gene that is frequently deleted or epigenetically silenced in many human cancers. However, the molecular function of HIC1 in pancreatic cancer has not been fully elucidated, especially in cancer invasion and metastasis. We aimed to clarify the clinical relevance of HIC1 and human pancreatic cancer and the mechanism of its effect on invasion and metastasis .HIC1 was downregulated in pancreatic cancer patient cancer tissue and pancreatic cancer cell lines. A tissue microarray analysis demonstrated that negative HIC1 expression predicted advanced pathological stages and worse patient survival. In addition, HIC1 inhibited the invasion and metastasis of pancreatic cancer cells both in vitro and in vivo. Finally, HIC1 repressed the expression of STAT3 target genes, including c-Myc, VEGF, CyclinD1, MMP2 and MMP9, by binding and interacting with STAT3 to impede its DNA-binding ability but without affecting the protein levels of STAT3 and p-STAT3. Therefore, HIC1 appears to function as a STAT3 inhibitor and may be a promising target for cancer research and for the development of an optimal treatment approach for pancreatic cancer.
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