| Literature DB >> 26238082 |
Ji Cheng1, Rui Deng1, Peng Zhang1, Chuanqing Wu1, Ke Wu1, Liang Shi1, Xinghua Liu1, Jie Bai1, Meizhou Deng1, Xiaoming Shuai1, Jinbo Gao1, Guobin Wang1, Kaixiong Tao1.
Abstract
Sall4 is a novel oncogene found upregulated in several malignancies including colon cancer. However, its upstream regulatory miRNA is still undefined. miR-219-5p is regarded as a tumor-related miRNA in cancer research. Nevertheless, its actual role of whether inhibiting or promoting tumorigenesis is unclear in colon cancer. Potential interaction between Sall4 and miR-219-5p is predicted by TargetScan. CCK-8 test was used for evaluation of cell proliferation and cell survival rates. Western blot analysis and real-time PCR were applied for detection of target molecules. Luciferase assay was a direct confirmation of mutual interaction. Wound healing assay and transwell assay were conducted for cell migration and invasion tests. Flow cytometry was used for cell apoptosis analysis. Tissue specimens and cell lines were explored for miR-219-5p inhibition on colon cancer proliferation, migration, invasion, apoptosis and drug resistance by targeting Sall4. The results show that miR-219-5p inhibited carcinogenesis of colon cancer by targeting oncogene Sall4.Entities:
Mesh:
Substances:
Year: 2015 PMID: 26238082 DOI: 10.3892/or.2015.4168
Source DB: PubMed Journal: Oncol Rep ISSN: 1021-335X Impact factor: 3.906