| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 2047620 | FEBS Letters | 2015 | 9 Pages |
•miR-1 suppresses the malignant properties of HCC in vitro and in vivo.•miR-1 and API-5 are inversely expressed in human primary HCC tissues.•miR-1 negatively regulates API-5 expression via binding to its 3′UTR.•miR-1 promotes apoptosis of hepatoma cells by directly targeting API-5.
Although microRNA-1 (miR-1) is a known liver cancer suppressor, the role of miR-1 in apoptosis of hepatoma cells has remained largely unknown. Our study shows that ectopic miR-1 overexpression induced apoptosis of liver hepatocellular carcinoma (HepG2) cells. Apoptosis inhibitor 5 (API-5) was found to be a potential regulator of miR-1 induced apoptosis, using a bioinformatics approach. Furthermore, an inverse relationship between miR-1 and API-5 expression was observed in human liver cancer tissues and adjacent normal liver tissues. Negative regulation of API-5 expression by miR-1 was demonstrated to promote apoptosis of HepG2 cells. Our study provides a novel regulatory mechanism of miR-1 in the apoptosis of hepatoma cells.
