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pmid:33731144

Identifying SLC27A5 as a potential prognostic marker of hepatocellular carcinoma by weighted gene co-expression network analysis and in vitro assays.

Fan Zhang · Mengjuan Xue · Xin Jiang · Huiyuan Yu · Yixuan Qiu · Jiaming Yu · Fan Yang · Zhijun Bao

Cancer cell international · 2021 doi:10.1186/s12935-021-01871-6

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Data

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pmid:33731144
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2026-11-01T15:41:29Z
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title
Identifying SLC27A5 as a potential prognostic marker of hepatocellular carcinoma by weighted gene co-expression network analysis and in vitro assays.
doi
10.1186/s12935-021-01871-6
pmid
33731144
authors array · 8 items
[0]
Fan Zhang
[1]
Mengjuan Xue
[2]
Xin Jiang
[3]
Huiyuan Yu
[4]
Yixuan Qiu
[5]
Jiaming Yu
[6]
Fan Yang
[7]
Zhijun Bao
journal
Cancer cell international
year
2021
abstract
BACKGROUND: The incidence and mortality rates of hepatocellular carcinoma are among the highest of all cancers all over the world. However the survival rates are relatively low due to lack of effective treatments. Efforts to elucidate the mechanisms of HCC and to find novel prognostic markers and therapeutic targets are ongoing. Here we tried to identify prognostic genes of HCC through co-expression network analysis. METHODS: We conducted weighted gene co-expression network analysis with a microarray dataset GSE14520 of HCC from Gene Expression Omnibus database and identified a hub module associated with HCC prognosis. Function enrichment analysis of the hub module was performed. Clinical information was analyzed to select candidate hub genes. The expression profiles and survival analysis of the selected genes were performed using additional datasets (GSE45267 and TCGA-LIHC) and the hub gene was identified. GSEA and in vitro experiments were conducted to further verify the function of the hub gene. RESULTS: Genes in the hub module were mostly involved in the metabolism pathway. Four genes (SLC27A5, SLC10A1, PCK2 and FMO4) from the module were identified as candidate hub genes according to correlation analysis with prognostic indicators. All these genes were significantly down-regulated in tumor tissues compared with non-tumor tissues in additional datasets. After survival analysis and network construction, SLC27A5 was selected as a prognostic marker. GSEA analysis and in vitro assays suggested that SLC27A5 downregulation promoted tumor cell migration via enhancing epithelial-mesenchymal transition. CONCLUSION: SLC27A5 is a potential biomarker of HCC and SLC27A5 downregulation promoted HCC progression by enhancing EMT.
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Overrepresentation analysis (ORA) based on the hypergeometric distribution was used as the gene set enrichment method.
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sections[7] "Gene ontology (GO) enrichment and Kyoto encyclopedia of genes and genomes (KEGG) pathway analysis of the hub module" paragraph 2
quote
Overrepresentation analysis (ORA) based on the hypergeometric distribution was used as the gene set enrichment method.
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The data supporting the findings of this study are available in GEO at https://www.ncbi.nlm.nih.gov/geo/, reference number GSE14520 and GSE45267, and in TCGA at https://portal.gdc.cancer.gov/, reference number TCGA-LIHC.
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sections[31] "notes" paragraph 1
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The data supporting the findings of this study are available in GEO at https://www.ncbi.nlm.nih.gov/geo/, reference number GSE14520 and GSE45267, and in TCGA at https://portal.gdc.cancer.gov/, reference number TCGA-LIHC.
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The data supporting the findings of this study are available in GEO at https://www.ncbi.nlm.nih.gov/geo/, reference number GSE14520 and GSE45267, and in TCGA at https://portal.gdc.cancer.gov/, reference number TCGA-LIHC.
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The data supporting the findings of this study are available in GEO at https://www.ncbi.nlm.nih.gov/geo/, reference number GSE14520 and GSE45267, and in TCGA at https://portal.gdc.cancer.gov/, reference number TCGA-LIHC.
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3921;571
taxon
Homo sapiens
title
Gene expression data of human hepatocellular carcinoma (HCC)
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2026-11-01T15:39:54Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
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The data supporting the findings of this study are available in GEO at https://www.ncbi.nlm.nih.gov/geo/, reference number GSE14520 and GSE45267, and in TCGA at https://portal.gdc.cancer.gov/, reference number TCGA-LIHC.
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Homo sapiens
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Gene expression profiles of human hepatocellular carcinoma (training set 1)
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Constructing weighted co-expression network
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d gene co-expression network analysis with a microarray dataset GSE14520 of HCC from Gene Expression
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d for the culture of HepG2 cells. Cells were cultured in a humidified environment consisting of 95% a
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ibco, Australia) was used for the culture of HepG2 cells. Cells were cultured in a humidified e
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:33731144", "kind": "science-record", "revision": 6, "content_hash": "sha256:3d9e8194d571150366b18b5e9d377e0b81d4ac1989958d9b8c6871e0321990b4", "created_at": "2026-11-01T15:41:29Z", "updated_at": "2026-11-01T21:24:53Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Identifying SLC27A5 as a potential prognostic marker of hepatocellular carcinoma by weighted gene co-expression network analysis and in vitro assays.", "doi": "10.1186/s12935-021-01871-6", "pmid": "33731144", "authors": ["Fan Zhang", "Mengjuan Xue", "Xin Jiang", "Huiyuan Yu", "Yixuan Qiu", "Jiaming Yu", "Fan Yang", "Zhijun Bao"], "journal": "Cancer cell international", "year": 2021, "abstract": "BACKGROUND: The incidence and mortality rates of hepatocellular carcinoma are among the highest of all cancers all over the world. However the survival rates are relatively low due to lack of effective treatments. Efforts to elucidate the mechanisms of HCC and to find novel prognostic markers and therapeutic targets are ongoing. Here we tried to identify prognostic genes of HCC through co-expression network analysis.\nMETHODS: We conducted weighted gene co-expression network analysis with a microarray dataset GSE14520 of HCC from Gene Expression Omnibus database and identified a hub module associated with HCC prognosis. Function enrichment analysis of the hub module was performed. Clinical information was analyzed to select candidate hub genes. The expression profiles and survival analysis of the selected genes were performed using additional datasets (GSE45267 and TCGA-LIHC) and the hub gene was identified. GSEA and in vitro experiments were conducted to further verify the function of the hub gene.\nRESULTS: Genes in the hub module were mostly involved in the metabolism pathway. Four genes (SLC27A5, SLC10A1, PCK2 and FMO4) from the module were identified as candidate hub genes according to correlation analysis with prognostic indicators. All these genes were significantly down-regulated in tumor tissues compared with non-tumor tissues in additional datasets. After survival analysis and network construction, SLC27A5 was selected as a prognostic marker. GSEA analysis and in vitro assays suggested that SLC27A5 downregulation promoted tumor cell migration via enhancing epithelial-mesenchymal transition.\nCONCLUSION: SLC27A5 is a potential biomarker of HCC and SLC27A5 downregulation promoted HCC progression by enhancing EMT.", "claims": [{"id": "claim-method", "statement": "Overrepresentation analysis (ORA) based on the hypergeometric distribution was used as the gene set enrichment method.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:33731144", "locator": "sections[7] \"Gene ontology (GO) enrichment and Kyoto encyclopedia of genes and genomes (KEGG) pathway analysis of the hub module\" paragraph 2", "quote": "Overrepresentation analysis (ORA) based on the hypergeometric distribution was used as the gene set enrichment method."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The data supporting the findings of this study are available in GEO at https://www.ncbi.nlm.nih.gov/geo/, reference number GSE14520 and GSE45267, and in TCGA at https://portal.gdc.cancer.gov/, reference number TCGA-LIHC.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:33731144", "locator": "sections[31] \"notes\" paragraph 1", "quote": "The data supporting the findings of this study are available in GEO at https://www.ncbi.nlm.nih.gov/geo/, reference number GSE14520 and GSE45267, and in TCGA at https://portal.gdc.cancer.gov/, reference number TCGA-LIHC."}], "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:33731144"], "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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