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pmid:36057607
Effects of Let-7c on the processing of hepatitis B virus associated liver diseases.
Like Zhang · Xia Jiang · Guiqi Wang · Tatsuo Kanda · Osamu Yokosuka · Congjie Zhai · Lei Zhang · Peng Liu · Zengren Zhao · Zhongxin Li
Infectious agents and cancer · 2022 doi:10.1186/s13027-022-00458-8
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Experiment
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Complete file
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The lin28B/Let-7c/MYC axis is associated with the occurrence of many cancers. Therefore, we aimed to illuminate the function of the lin28B/Let-7c/MYC axis in hepatocellular carcinoma. We aimed to evaluate the critical involvement of lin28B and Let-7c in the carcinogenesis of human hepatocellular carcinoma (B-HCC).\nMETHODS: Data from the GEO database were used to analyse differentially expressed genes and IRGs. A protein - protein interaction (PPI) network and Venn diagram were generated to analyse relationships. Real-time RT-PCR, Western blotting, and cell counting kit-8 assays were used to examine the association of lin28B, Let-7c, and MYC with cell proliferation.\nRESULTS: A total of 2552 functionally annotated differentially expressed RNAs were analysed in HBV patients from the GSE135860 database. In addition, 46 let-7c target genes were screened in HBV patients, and the interactions were analysed through PPI network analysis. The results confirmed that Let-7c and its target genes play a key role in HBV-related diseases. Next, we discovered a gradual decrease in Let-7c expression during the progression from HBV-associated chronic hepatitis (B-CH) and HBV-associated liver cirrhosis (B-LC) to B-HCC. We found evidence for a negative association between lin28B expression and Let-7c expression. The expression of MYC was obviously upregulated when Let-7c was inhibited.\nCONCLUSION: Our results highlight that Let-7c and lin28B participate in the carcinogenesis of HBV-associated diseases through the lin28B/Let-7c/MYC axis.", "claims": [{"id": "claim-method", "statement": "R software’s limma package was used to carry out the differential gene analysis. 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Real-time RT-PCR, Western blotting, and cell counting kit-8 assays were used to"], "order_basis": "paper_text_order:709", "id": "assay:1"}, {"role": "data_generation", "definition_id": "cell_culture", "definition_version": "99e1195c7d6f", "definition_digest": null, "required_operations": [], "support_state": "partial", "source_hashes": {"assay_lexicon": "99e1195c7d6f"}, "confidence": 0.99, "evidence": ["ichuan Medical College, Nanchong, China). We cultured human hepatoma HepG2 cells in Dulbecco’s mod", ", calculated by Chi-square test Cell culture HepG2.2.15 cells containing the complete HBV genom", "Nanchong, China). We cultured human hepatoma HepG2 cells in Dulbecco’s modified Eagle’s medium,", "CH serum samples. c Let-7c expression in the HepG2 group and HepG2.2.15 group. The last group w"], "order_basis": "paper_text_order:4169", "id": "assay:2"}, {"role": "data_generation", "definition_id": "qpcr", "definition_version": "99e1195c7d6f", "definition_digest": null, "required_operations": [], "support_state": "partial", "source_hashes": {"assay_lexicon": "99e1195c7d6f"}, "confidence": 0.99, "evidence": ["tion of lin28B in the B-HCC samples. We used real-time PCR to detect expression. Overall, the results w", "fected by HBV. 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