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pmid:37065781

Integrated analysis of multiple transcriptomic data identifies ST8SIA6‑AS1 and LINC01093 as potential biomarkers in HBV‑associated liver cancer.

Jianhua Xue · Hui Zhao · Yifei Fu · Xu Liu · Xiangxiang Wu

Oncology letters · 2023 doi:10.3892/ol.2023.13771

Paper

complete

Experiment

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Data

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Analysis

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Execution

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pmid:37065781
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title
Integrated analysis of multiple transcriptomic data identifies ST8SIA6‑AS1 and LINC01093 as potential biomarkers in HBV‑associated liver cancer.
doi
10.3892/ol.2023.13771
pmid
37065781
authors array · 5 items
[0]
Jianhua Xue
[1]
Hui Zhao
[2]
Yifei Fu
[3]
Xu Liu
[4]
Xiangxiang Wu
journal
Oncology letters
year
2023
abstract
The mechanisms of long-non-coding RNAs (lncRNAs) in hepatitis B virus (HBV) infection-associated liver cancer remain largely unclear. Therefore, the aim of the present study was to investigate the regulatory mechanisms of lncRNAs in this disease. HBV-liver cancer related transcriptome expression profile data (GSE121248 and GSE55092) from the Gene Expression Omnibus database and survival prognosis information from The Cancer Genome Atlas (TCGA) database were obtained for analysis. The limma package was used to identify the overlapped differentially expressed RNAs (DERs), including DElncRNAs and DEmRNAs, in the GSE121248 and GSE55092 datasets. The screened optimized lncRNA signatures were used to develop a nomogram model based on the GSE121248 dataset, which was validated using the GSE55092 and TCGA datasets. A competitive endogenous RNA (ceRNA) network was constructed based on the screened prognosis-associated lncRNA signatures from TCGA dataset. In addition, the levels of specific lncRNAs were evaluated in HBV-infected human liver cancer tissues and cells, and Cell Counting Kit-8, ELISA and Transwell assays were performed to evaluate the effects of the lncRNAs in HBV-expressing liver cancer cells. A total of 535 overlapped DERs, including 30 DElncRNAs and 505 DEmRNAs, were identified in the GSE121248 and GSE55092 datasets. An optimized DElncRNA signature comprising 10 lncRNAs was used to establish a nomogram. ST8SIA6-AS1 and LINC01093 were identified as lncRNAs associated with HBV-liver cancer prognosis in TCGA dataset, and were applied to construct a ceRNA network. Reverse transcription-quantitative PCR analysis showed that ST8SIA6-AS1 was upregulated and LINC01093 was downregulated in HBV-infected human liver cancer tissues and HBV-expressing liver cancer cells compared with non-HBV-infected controls. ST8SIA6-AS1 knockdown and LINC01093 overexpression independently reduced the number of copies of HBV DNA, the levels of hepatitis B surface antigen and hepatitis B e antigen, as well as cell proliferation, migration and invasion. In summary, the present study identified ST8SIA6-AS1 and LINC01093 as two potential biomarkers that may be effective therapeutic targets for HBV-associated liver cancer.
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sections[4] "Screening of overlapped differentially expressed RNAs (DERs)" paragraph 2
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The limma package of R3.6.1 version 3.34.7 (20) was utilized to screen the DERs, including DElncRNAs and DEmRNAs, between the HBV-liver cancer and normal control groups in GSE121248 and GSE55092.
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sections[4] "Screening of overlapped differentially expressed RNAs (DERs)" paragraph 2
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The limma package of R3.6.1 version 3.34.7 (20) was utilized to screen the DERs, including DElncRNAs and DEmRNAs, between the HBV-liver cancer and normal control groups in GSE121248 and GSE55092.
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Gene expression profiling of chronic hepatitis B induced HCC and adjacent-normal tissues
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type
dataset
label
GEO GSE121248
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agent:corpus-assay-engine
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extraction
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agent:minimax-reader
[2] object · 4 fields
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activity-resolve-GSE121248
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accession_resolution
used array · 1 item
[0]
data:geo:GSE121248
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agent:corpus-assay-engine
agents array · 2 items
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agent:corpus-assay-engine
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software
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agent:minimax-reader
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software
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source_run_id
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dsl_catalogue_fingerprint
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capability_table_fingerprint
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lineage object · 4 fields
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fork_of
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gaps array · 9 items
[0]
asset:data:geo:GSE121248 licence not read
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asset:data:geo:GSE121248 not downloaded
[2]
asset:data:geo:GSE55092 licence not read
[3]
asset:data:geo:GSE55092 not downloaded
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execution.not_run
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method.reader_differs_from_extractor
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review.human_critique
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review.independent_reader
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review.machine_critique
assays array · 3 items
[0] object · 11 fields
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data_generation
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support_state
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source_hashes object · 1 field
assay_lexicon
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confidence
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evidence array · 1 item
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tissues and cells, and Cell Counting Kit-8, ELISA and Transwell assays were performed to evalu
order_basis
paper_text_order:1199
id
assay:1
[1] object · 11 fields
role
data_generation
definition_id
transfection
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required_operations array · 0 items
support_state
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assay_lexicon
99e1195c7d6f
confidence
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evidence array · 1 item
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with non-HBV-infected controls. ST8SIA6-AS1 knockdown and LINC01093 overexpression independently r
order_basis
paper_text_order:1948
id
assay:2
[2] object · 11 fields
role
analysis
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differential_expression
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required_operations array · 3 items
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evidence array · 1 item
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The limma package of R3.6.1 version 3.34.7 (20) was utilized to screen the DERs, including DElncRNAs and DEmRNAs, between the HBV-liver cancer and normal control groups in GSE121248 and GSE55092.
order_basis
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:37065781", "kind": "science-record", "revision": 4, "content_hash": "sha256:c58b3612d3de9e2cf6f077d15603c0f5add2407f65fadee8f774d163629bdbd8", "created_at": "2026-11-01T19:01:43Z", "updated_at": "2026-11-01T22:51:43Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Integrated analysis of multiple transcriptomic data identifies ST8SIA6‑AS1 and LINC01093 as potential biomarkers in HBV‑associated liver cancer.", "doi": "10.3892/ol.2023.13771", "pmid": "37065781", "authors": ["Jianhua Xue", "Hui Zhao", "Yifei Fu", "Xu Liu", "Xiangxiang Wu"], "journal": "Oncology letters", "year": 2023, "abstract": "The mechanisms of long-non-coding RNAs (lncRNAs) in hepatitis B virus (HBV) infection-associated liver cancer remain largely unclear. Therefore, the aim of the present study was to investigate the regulatory mechanisms of lncRNAs in this disease. HBV-liver cancer related transcriptome expression profile data (GSE121248 and GSE55092) from the Gene Expression Omnibus database and survival prognosis information from The Cancer Genome Atlas (TCGA) database were obtained for analysis. The limma package was used to identify the overlapped differentially expressed RNAs (DERs), including DElncRNAs and DEmRNAs, in the GSE121248 and GSE55092 datasets. The screened optimized lncRNA signatures were used to develop a nomogram model based on the GSE121248 dataset, which was validated using the GSE55092 and TCGA datasets. A competitive endogenous RNA (ceRNA) network was constructed based on the screened prognosis-associated lncRNA signatures from TCGA dataset. In addition, the levels of specific lncRNAs were evaluated in HBV-infected human liver cancer tissues and cells, and Cell Counting Kit-8, ELISA and Transwell assays were performed to evaluate the effects of the lncRNAs in HBV-expressing liver cancer cells. A total of 535 overlapped DERs, including 30 DElncRNAs and 505 DEmRNAs, were identified in the GSE121248 and GSE55092 datasets. An optimized DElncRNA signature comprising 10 lncRNAs was used to establish a nomogram. ST8SIA6-AS1 and LINC01093 were identified as lncRNAs associated with HBV-liver cancer prognosis in TCGA dataset, and were applied to construct a ceRNA network. Reverse transcription-quantitative PCR analysis showed that ST8SIA6-AS1 was upregulated and LINC01093 was downregulated in HBV-infected human liver cancer tissues and HBV-expressing liver cancer cells compared with non-HBV-infected controls. ST8SIA6-AS1 knockdown and LINC01093 overexpression independently reduced the number of copies of HBV DNA, the levels of hepatitis B surface antigen and hepatitis B e antigen, as well as cell proliferation, migration and invasion. In summary, the present study identified ST8SIA6-AS1 and LINC01093 as two potential biomarkers that may be effective therapeutic targets for HBV-associated liver cancer.", "claims": [{"id": "claim-method", "statement": "The limma package of R3.6.1 version 3.34.7 (20) was utilized to screen the DERs, including DElncRNAs and DEmRNAs, between the HBV-liver cancer and normal control groups in GSE121248 and GSE55092.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:37065781", "locator": "sections[4] \"Screening of overlapped differentially expressed RNAs (DERs)\" paragraph 2", "quote": "The limma package of R3.6.1 version 3.34.7 (20) was utilized to screen the DERs, including DElncRNAs and DEmRNAs, between the HBV-liver cancer and normal control groups in GSE121248 and GSE55092."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:37065781", "locator": "sections[27] \"Availability of data and materials\" paragraph 2", "quote": "The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request."}], "state": "complete"}, {"id": "claim-target-result", "statement": "The limma package was used to screen differentially expressed RNAs between HBV-liver cancer and normal control groups in the GSE121248 and GSE55092 datasets.", "kind": "quantitative", "target": {"value": 3.6, "unit": "correlation coefficient", "tolerance": null, "source": "The limma package of R3.6.1 version 3.34.7 (20) was utilized to screen the DERs, including DElncRNAs and DEmRNAs, between the HBV-liver cancer and normal control groups in GSE121248 and GSE55092."}, "evidence": [{"asset": "source:pmid:37065781", "locator": "sections[4] \"Screening of overlapped differentially expressed RNAs (DERs)\" paragraph 2", "quote": "The limma package of R3.6.1 version 3.34.7 (20) was utilized to screen the DERs, including DElncRNAs and DEmRNAs, between the HBV-liver cancer and normal control groups in GSE121248 and GSE55092."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "The limma package was used to screen differentially expressed RNAs between HBV-liver cancer and normal control groups in the GSE121248 and GSE55092 datasets.", "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:37065781"], "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. This lane did not download the dataset or read its licence.", "duration_hours": null, "parameters": {}, "inputs": ["data:geo:GSE121248"], "outputs": ["the source data with its repository provenance"], "instruments": [], "reagents": []}, {"id": "run_analysis", "order": 3, "name": "Run the published analysis", "kind": "analysis", "state": "complete", "blocked_on": null, "description": "Apply the paper's statistical method to the resolved series and compare the result with the published target.", "duration_hours": null, "parameters": {}, "inputs": ["data:geo:GSE121248"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:37065781", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.3892/ol.2023.13771", "sha256": 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