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miR-219-5p plays a tumor suppressive role in colon cancer by targeting oncogene Sall4
Author(s) -
Ji Cheng,
Rui Deng,
Peng Zhang,
Chuanqing Wu,
Ke Wu,
Liang Shi,
Xinghua Liu,
Jie Bai,
Meizhou Deng,
Xiaoming Shuai,
Jinbo Gao,
Guobin Wang,
Kaixiong Tao
Publication year - 2015
Publication title -
oncology reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.094
H-Index - 96
eISSN - 1791-2431
pISSN - 1021-335X
DOI - 10.3892/or.2015.4168
Subject(s) - oncogene , carcinogenesis , cancer research , molecular medicine , cell cycle , cancer , microrna , cell growth , colorectal cancer , biology , apoptosis , cell , flow cytometry , immunology , gene , biochemistry , genetics
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.

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