| Literature DB >> 27085461 |
Bin Hu1, Kundong Zhang2, Shaobo Li3, Hao Li2, Zhaowen Yan3, Li Huang1, Jianghong Wu1, Xiao Han1, Weiliang Jiang1, Tunike Mulatibieke1, Lin Zheng3, Rong Wan1, Xingpeng Wang4, Guoyong Hu5.
Abstract
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.Entities:
Keywords: HIC1; IL-6/STAT3; Invasion; Metastasis; Pancreatic cancer
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Year: 2016 PMID: 27085461 DOI: 10.1016/j.canlet.2016.04.013
Source DB: PubMed Journal: Cancer Lett ISSN: 0304-3835 Impact factor: 8.679