Aberrant expression of two miRNAs promotes proliferation, hepatitis B virus amplification, migration and invasion of hepatocellular carcinoma cells: evidence from bioinformatic analysis and experimental validation.

{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:32377460", "kind": "science-record", "revision": 8, "content_hash": "sha256:2379c5d5803d9f2ed4a0d613b150c43f83126bcd3f66c5c487efe7493dc4d1c2", "created_at": "2026-11-01T15:41:01Z", "updated_at": "2026-11-01T22:44:49Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Aberrant expression of two miRNAs promotes proliferation, hepatitis B virus amplification, migration and invasion of hepatocellular carcinoma cells: evidence from bioinformatic analysis and experimental validation.", "doi": "10.7717/peerj.9100", "pmid": "32377460", "authors": ["Yanming Liu", "Yue Cao", "Wencan Cai", "Liangyin Wu", "Pingsen Zhao", "Xin-Guang Liu"], "journal": "PeerJ", "year": 2020, "abstract": "BACKGROUND: As key negative regulators of gene expression, microRNAs (miRNAs) play an important role in the onset and progression of hepatocellular carcinoma (HCC). This study aimed to identify the miRNAs involved in HCC carcinogenesis and their regulated genes.\nMETHODS: The Gene Expression Omnibus (GEO) dataset (GSE108724) was chosen and explored to identify differentially expressed miRNAs using GEO2R. For the prediction of potential miRNA target genes, the miRTarBase was explored. Enrichment analysis of Gene Ontology (GO) and the Kyoto Encyclopedia of Genes and Genomes (KEGG) was performed by the DAVID online tool. The hub genes were screened out using the CytoHubba plug-in ranked by degrees. The networks between miRNAs and hub genes were constructed by Cytoscape software. MiRNA mimics and negative control were transfected into HCC cell lines and their effects on proliferation, hepatitis B virus DNA (HBV-DNA) replication, TP53 expression, migration, and invasion were investigated. The following methods were employed: MTT assay, quantitative PCR (qPCR) assay, western blotting, wound healing assay, and transwell assay.\nRESULTS: A total of 50 differentially expressed miRNAs were identified, including 20 upregulated and 30 downregulated miRNAs, in HCC tumor tissues compared to matched adjacent tumor-free tissues. The top three upregulated (miR-221-3p, miR-222-3p, and miR-18-5p) and downregulated (miR-375, miR-214-3p and miR-378d) miRNAs, ranked by |log2 fold change (log2FC)|, were chosen and their potential target genes were predicted. Two gene sets, targeted by the upregulated and the downregulated miRNAs, were identified respectively. GO and KEGG pathway analysis showed that the predicted target genes of upregulated and downregulated miRNAs were mainly enriched in the cell cycle and cancer-related pathways. The top ten hub nodes of gene sets ranked by degrees were identified as hub genes. Analysis of miRNA-hub gene network showed that miR-221-3p and miR-375 modulated most of the hub genes, especially involving regulation of TP53. The q-PCR results showed that miR-221-3p and miR-375 were markedly upregulated and downregulated, respectively, in HCC cells and HCC clinical tissue samples compared to non-tumoral tissues. Furthermore, miR-221-3p overexpression significantly enhanced proliferation, HBV-DNA replication, as well as the migration and invasion of HCC cells, whereas miR-375 overexpression resulted in opposite effects. Western blotting analysis showed that the overexpression of miR-221-3p and miR-375 reduced and increased TP53 expression, respectively.\nCONCLUSION: The present study revealed that miR-211-3p and miR-375 may exert vital effects on cell proliferation, HBV-DNA replication, cell migration, and invasion through the regulation of TP53 expression in HCC.", "claims": [{"id": "claim-data-access", "statement": "The raw measurements are available in the Supplemental Files.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:32377460", "locator": "sections[25] \"Additional Information and Declarations\" paragraph 5", "quote": "The raw measurements are available in the Supplemental Files."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": null, "steps": [{"id": "read_published_estimate", "order": 1, "name": "Read the published estimate from the source", "kind": "other", "state": "complete", "blocked_on": null, "description": "The claim, method and evidence span published with the source article.", "duration_hours": null, "parameters": {}, "inputs": ["source:pmid:32377460"], "outputs": ["the published estimate and its evidence"], "instruments": [], "reagents": []}, {"id": "obtain_source_data", "order": 2, "name": "Obtain the source data from the named repository", "kind": "data-preparation", "state": "complete", "blocked_on": null, "description": "The GEO series accession resolves and its sample accessions are listed. 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MiRNA mimics and negative control were transfected into HCC cell lines and their effects on pro", ". HCC cell lines, clinical samples, and cell transfection Immortalized normal human liver HL7702 cells", "manufacturer’s instructions, the riboFECT CP Transfection Kit (C10511-05; RiboBio, Guangzhou, China) w"], "order_basis": "paper_text_order:995", "id": "assay:1"}, {"role": "data_generation", "definition_id": "apoptosis_assay", "definition_version": "99e1195c7d6f", "definition_digest": null, "required_operations": [], "support_state": "partial", "source_hashes": {"assay_lexicon": "99e1195c7d6f"}, "confidence": 0.93, "evidence": ["igated. The following methods were employed: MTT assay, quantitative PCR (qPCR) assay, wester"], "order_basis": "paper_text_order:1205", "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": 0.93, "evidence": ["were employed: MTT assay, quantitative PCR (qPCR) assay, western blotting, wound healing assa"], "order_basis": "paper_text_order:1235", "id": "assay:3"}, {"role": "data_generation", "definition_id": "western_blot", "definition_version": "99e1195c7d6f", "definition_digest": null, "required_operations": [], "support_state": "partial", "source_hashes": {"assay_lexicon": "99e1195c7d6f"}, "confidence": 0.99, "evidence": ["d: MTT assay, quantitative PCR (qPCR) assay, western blotting, wound healing assay, and transwell assay. R", "overexpression resulted in opposite effects. Western blotting analysis showed that the overexpression of m"], "order_basis": "paper_text_order:1247", "id": "assay:4"}, {"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": ["Co., Ltd. (Guangzhou, China). All cells were cultured in Dulbecco’s modified Eagle’s medium/High Gluc", "an liver HL7702 cells and the HCC cell lines HepG2, HepG2.2.15, and MHCC-LM3 were purchased fro", "r HL7702 cells and the HCC cell lines HepG2, HepG2.2.15, and MHCC-LM3 were purchased from Cellc", "s and clinical samples Three HCC cell lines (HepG2, HepG2.2.15, and HCC-LM3) and a normal liver"], "order_basis": "paper_text_order:4210", "id": "assay:5"}, {"role": "analysis", "definition_id": "differential_expression", "definition_version": "f2132e96ae6c7a4e", "definition_digest": null, "required_operations": ["normalise_counts", "differential_expression_fit", "fdr_bh"], "support_state": "supported", "source_hashes": {"dsl_catalogue": "f2132e96ae6c7a4e"}, "confidence": 1.0, "evidence": ["“The DE-miRNAs between HCC and matched adjacent tumor-free tissues were screened using GEO2R (http://www.ncbi.nlm.nih.gov/geo/geo2r) according to the cut-off criterion that P-value < 0.05 and |log2 fold change (log2FC)| > 2, an online interactive web tool with built-in GEOquery and limma R packages that allows to compare two or more datasets across experimental conditions.”"], "order_basis": "consumes_earlier_output", "id": "assay:6"}]}