MiR-18a-5p Facilitates Progression of Hepatocellular Carcinoma by Targeting CPEB3
Objective: To explore the function of the miR-18a-5p/CPEB3 axis in regulating the occurrence of hepatocellular carcinoma (HCC). Methods: Differentially expressed miRNAs and mRNAs were acquired by bioinformatics analysis. qRT-PCR was used for miR-18a-5p and CPEB3 mRNA expression detection. Cell funct...
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SAGE Publishing
2021
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oai:doaj.org-article:d13529c889cf421d859dfe77aae6f6d72021-11-05T22:33:23ZMiR-18a-5p Facilitates Progression of Hepatocellular Carcinoma by Targeting CPEB31533-033810.1177/15330338211043976https://doaj.org/article/d13529c889cf421d859dfe77aae6f6d72021-11-01T00:00:00Zhttps://doi.org/10.1177/15330338211043976https://doaj.org/toc/1533-0338Objective: To explore the function of the miR-18a-5p/CPEB3 axis in regulating the occurrence of hepatocellular carcinoma (HCC). Methods: Differentially expressed miRNAs and mRNAs were acquired by bioinformatics analysis. qRT-PCR was used for miR-18a-5p and CPEB3 mRNA expression detection. Cell functional assays were implemented to examine the biological functions of HCC cells. The binding relationship between miR-18a-5p and CPEB3 was verified by a dual luciferase assay. Results: In HCC, miR-18a-5p was remarkably highly expressed, while CPEB3 was markedly lowly expressed. HCC cell progression was facilitated after cells transfecting miR-18a-5p mimic, whereas silencing miR-18a-5p caused the opposite result. Overexpressing CPEB3 could restore promoting effect of miR-18a-5p on the growth of HCC cells. Conclusion: Oncogene miR-18a-5p accelerates malignant phenotype by suppressing CPEB3. MiR-18a-5p/CPEB3 axis in HCC identified in this study provides a new target for HCC treatment.Mingxin Cui MMFengzhi Qu MMLibing Wang MMDaming Cheng MBXiaogang Liu MMSAGE PublishingarticleNeoplasms. Tumors. Oncology. Including cancer and carcinogensRC254-282ENTechnology in Cancer Research & Treatment, Vol 20 (2021) |
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Neoplasms. Tumors. Oncology. Including cancer and carcinogens RC254-282 |
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Neoplasms. Tumors. Oncology. Including cancer and carcinogens RC254-282 Mingxin Cui MM Fengzhi Qu MM Libing Wang MM Daming Cheng MB Xiaogang Liu MM MiR-18a-5p Facilitates Progression of Hepatocellular Carcinoma by Targeting CPEB3 |
description |
Objective: To explore the function of the miR-18a-5p/CPEB3 axis in regulating the occurrence of hepatocellular carcinoma (HCC). Methods: Differentially expressed miRNAs and mRNAs were acquired by bioinformatics analysis. qRT-PCR was used for miR-18a-5p and CPEB3 mRNA expression detection. Cell functional assays were implemented to examine the biological functions of HCC cells. The binding relationship between miR-18a-5p and CPEB3 was verified by a dual luciferase assay. Results: In HCC, miR-18a-5p was remarkably highly expressed, while CPEB3 was markedly lowly expressed. HCC cell progression was facilitated after cells transfecting miR-18a-5p mimic, whereas silencing miR-18a-5p caused the opposite result. Overexpressing CPEB3 could restore promoting effect of miR-18a-5p on the growth of HCC cells. Conclusion: Oncogene miR-18a-5p accelerates malignant phenotype by suppressing CPEB3. MiR-18a-5p/CPEB3 axis in HCC identified in this study provides a new target for HCC treatment. |
format |
article |
author |
Mingxin Cui MM Fengzhi Qu MM Libing Wang MM Daming Cheng MB Xiaogang Liu MM |
author_facet |
Mingxin Cui MM Fengzhi Qu MM Libing Wang MM Daming Cheng MB Xiaogang Liu MM |
author_sort |
Mingxin Cui MM |
title |
MiR-18a-5p Facilitates Progression of Hepatocellular Carcinoma by Targeting CPEB3 |
title_short |
MiR-18a-5p Facilitates Progression of Hepatocellular Carcinoma by Targeting CPEB3 |
title_full |
MiR-18a-5p Facilitates Progression of Hepatocellular Carcinoma by Targeting CPEB3 |
title_fullStr |
MiR-18a-5p Facilitates Progression of Hepatocellular Carcinoma by Targeting CPEB3 |
title_full_unstemmed |
MiR-18a-5p Facilitates Progression of Hepatocellular Carcinoma by Targeting CPEB3 |
title_sort |
mir-18a-5p facilitates progression of hepatocellular carcinoma by targeting cpeb3 |
publisher |
SAGE Publishing |
publishDate |
2021 |
url |
https://doaj.org/article/d13529c889cf421d859dfe77aae6f6d7 |
work_keys_str_mv |
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1718444010184376320 |