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MicroRNA-18a Targets IRF2 and CBX7 to Promote Cell Proliferation in Hepatocellular Carcinoma
MicroRNAs (miRNAs) are a family of noncoding RNAs of ∼22 nt in length that play important roles in the tumor initiation and progression processes. The aberrant expression status of miR-18a has been reported in hepatocellular carcinoma (HCC). However, the biological role and the underlying me...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cognizant Communication Corporation
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7844746/ https://www.ncbi.nlm.nih.gov/pubmed/29386090 http://dx.doi.org/10.3727/096504018X15165493852990 |
Sumario: | MicroRNAs (miRNAs) are a family of noncoding RNAs of ∼22 nt in length that play important roles in the tumor initiation and progression processes. The aberrant expression status of miR-18a has been reported in hepatocellular carcinoma (HCC). However, the biological role and the underlying mechanism of miR-18a in HCC progression are still to be elucidated. In this study, we examined the expression level of miR-18a in HCC cell lines using the quantitative real-time PCR method. We showed that miR-18a expression in human HCC cell lines was elevated compared with the normal liver cell line. Meanwhile, increasing miR-18a expression by an miR-18a mimic in HCC cell lines promoted cell proliferation and migration, while inhibiting miR-18a expression by an miR-18a inhibitor caused the opposite effects. Using the bioinformatic analyses method, we found that the 3′-untranslated regions (3′-UTRs) of interferon regulatory factor 2 (IRF2) and chromobox protein homolog 7 (CBX7) contain putative binding sequences for miR-18a. Further, luciferase assay validated that both IRF2 and CBX7 were the direct targets of miR-18a in HCC. Moreover, we revealed that overexpression of IRF2 and CBX7 has similar effects as miR-18a downregulation on HCC cell lines. Our results illustrated that miR-18a plays a positive role in HCC progression process by stimulating cell proliferation and migration partly through regulating IRF2 and CBX7. |
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