Unknown

Dataset Information

0

Downregulated miR-621 promotes cell proliferation via targeting CAPRIN1 in hepatocellular carcinoma.


ABSTRACT: MicroRNAs (miRNAs) have been reported to play an essential role in tumor development and progression. However, the function of miR-621 in hepatocellular carcinoma (HCC) remains largely unexplored. In this study, we found that miR-621 was downregulated in the HCC specimens and cell lines, and lower expression of miR-621 indicated poor survival. Overexpression of miR-621 was shown to induce G0/G1 cell cycle arrest and inhibit cell proliferation in vitro and in vivo. Luciferase assays revealed that cell cycle-associated protein 1 (CAPRIN1) is a novel functional downstream target of miR-621. miR-621 could regulate c-MYC and cyclin D2 expression by directly targeting CAPRIN1. Further study revealed that CAPRIN1 was upregulated in the HCC specimens and cell lines. Restoration of CAPRIN1 neutralized the miR-621-induced cell cycle arrest and cell proliferation inhibition. Taken together, our findings suggest that miR-621 acts as a tumor suppressor gene in HCC progression by downregulating CAPRIN1 expression and could be a novel potential diagnostic and prognostic biomarker for HCC.

SUBMITTER: Zhang Y 

PROVIDER: S-EPMC6220141 | biostudies-literature | 2018

REPOSITORIES: biostudies-literature

altmetric image

Publications

Downregulated miR-621 promotes cell proliferation via targeting CAPRIN1 in hepatocellular carcinoma.

Zhang Yao Y   You Wei W   Zhou Haoming H   Chen Zhiqiang Z   Han Guoyong G   Zuo Xueliang X   Zhang Long L   Wu Jindao J   Wang Xuehao X  

American journal of cancer research 20181001 10


MicroRNAs (miRNAs) have been reported to play an essential role in tumor development and progression. However, the function of miR-621 in hepatocellular carcinoma (HCC) remains largely unexplored. In this study, we found that miR-621 was downregulated in the HCC specimens and cell lines, and lower expression of miR-621 indicated poor survival. Overexpression of miR-621 was shown to induce G0/G1 cell cycle arrest and inhibit cell proliferation <i>in vitro</i> and <i>in vivo</i>. Luciferase assays  ...[more]

Similar Datasets

| S-EPMC7960996 | biostudies-literature
| S-EPMC6535842 | biostudies-literature
| S-EPMC6549920 | biostudies-literature
| S-EPMC7864765 | biostudies-literature
| S-EPMC6825988 | biostudies-literature
| S-EPMC6495981 | biostudies-literature
| S-EPMC8668908 | biostudies-literature
| S-EPMC6501494 | biostudies-literature
| S-EPMC4767473 | biostudies-literature
| S-EPMC6323674 | biostudies-other