MicroRNA regulation of DNA repair gene expression in 4-aminobiphenyl-treated HepG2 cells
Autor: | Chi Yao Chang, Jong C. Wu, Yi Kuang Tsen, Nianhan Ma, Lin Chen Huan, Ssu Ching Chen, Bin Hao Chiou, Chin Hui Chen |
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Rok vydání: | 2014 |
Předmět: |
DNA Repair
DNA damage DNA repair Cell Survival Blotting Western Gene Expression Toxicology LIG1 Real-Time Polymerase Chain Reaction FANCG Aminobiphenyl Compounds Humans RNA Messenger Gene In Situ Hybridization Gene knockdown biology Molecular biology Proliferating cell nuclear antigen Culture Media Comet assay biology.protein Carcinogens RNA Comet Assay DNA Damage |
Zdroj: | Toxicology. 322 |
ISSN: | 1879-3185 |
Popis: | We examined the role of miRNAs in DNA damage response in HepG2 cells following exposure to 4-aminobiphenyl (4-ABP). The arylamine 4-ABP is a human carcinogen. Using the Comet assay, we showed that 4-ABP (18.75-300μM) induces DNA damage in HepG2 cells after 24h. DNA damage signaling pathway-based PCR arrays were used to investigate expression changes in genes involved in DNA damage response. Results showed down-regulation of 16 DNA repair-related genes in 4-ABP-treated cells. Among them, the expression of selected six genes (UNG, LIG1, EXO1, XRCC2, PCNA, and FANCG) from different DNA repair pathways was decreased with quantitative real-time PCR (qRT-PCR). In parallel, using the miRNA array, we reported that the expression of 27 miRNAs in 4-ABP-treated cells was at least 3-fold higher than that in the control group. Of these differential 27 miRNAs, the most significant expression of miRNA-513a-5p and miRNA-630 was further validated by qRT-PCR, and was predicted to be implicated in the deregulation of FANCG and RAD18 genes, respectively, via bioinformatic analysis. Both FANCG and RAD18 proteins were found to be down-regulated in 4-ABP-treated cells. In addition, overexpression and knockdown of miRNA-513a-5p and miRNA-630 reduced and increased the expression of FANCG and RAD18 proteins, respectively. Based on the above results, we indicated that miRNA-513a-5p and miRNA-630 could play a role in the suppression of DNA repair genes, and eventually lead to DNA damage. |
Databáze: | OpenAIRE |
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