Abstract |
The long non-coding FGD5-AS1 (LncFGD5-AS1) has been reported to be a novel carcinogenic gene and participant in regulating tumor progression by sponging microRNAs ( miRNAs). However, the pattern of expression and the biological role of FGD5-AS1 in hepatocellular carcinoma (HCC) remains largely unknown. The expression level of FGD5-AS1 in tumor tissues and cell lines was measured by RT-qPCR. CCK-8, EdU, flow cytometry, wound healing, and transwell chamber assays were performed to investigate the role of FGD5-AS1 in cell proliferation, apoptosis, migration, and invasion in HCC. Dual luciferase reporter, and RNA pull-down assays were performed to identify the regulatory interactions among FGD5-AS1, miR-873-5p and GTP-binding protein 4 (GTPBP4). We found that the expression of FGD5-AS1 was upregulated in HCC tissues and cell lines. Moreover, the knockdown of FGD5-AS1 suppressed cell proliferation, migration and invasion, and induced apoptosis in HCC cells. Further studies demonstrated that FGD5-AS1 could function as a competitive RNA by sponging miR-873-5p in HCC cells. Moreover, GTPBP4 was identified as direct downstream target of miR-873-5p in HCC cells and FGD5-AS1mediated the effects of GTPBP4 by competitively binding with miR-873-5p. Taken together, this study demonstrated the regulatory role of FGD5-AS1 in the progression of HCC and identified the miR-873-5p/GTPBP4 axis as the direct downstream pathway. It represents a promising novel therapeutic strategy for HCC patients.
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Authors | Nuobei Zhang, Hao Shen, Shenan Huang, Fenfen Wang, Huifang Liu, Fen Xie, Lei Jiang, Xin Chen |
Journal | European journal of histochemistry : EJH
(Eur J Histochem)
Vol. 65
Issue 4
(Nov 16 2021)
ISSN: 2038-8306 [Electronic] Italy |
PMID | 34783233
(Publication Type: Journal Article)
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Chemical References |
- MIRN873 microRNA, human
- MicroRNAs
- Neoplasm Proteins
- Nuclear Proteins
- RNA, Long Noncoding
- RNA, Neoplasm
- GTP-Binding Proteins
- GTPBP4 protein, human
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Topics |
- Carcinoma, Hepatocellular
(genetics, metabolism)
- GTP-Binding Proteins
(biosynthesis, genetics)
- Gene Expression Regulation, Neoplastic
- Hep G2 Cells
- Humans
- Liver Neoplasms
(genetics, metabolism)
- MicroRNAs
(biosynthesis, genetics)
- Neoplasm Proteins
(biosynthesis, genetics)
- Nuclear Proteins
(biosynthesis, genetics)
- Oncogenes
- RNA, Long Noncoding
(genetics, metabolism)
- RNA, Neoplasm
(genetics, metabolism)
- Up-Regulation
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