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pmid:32337286

Identification of Potential Biomarkers for Thyroid Cancer Using Bioinformatics Strategy: A Study Based on GEO Datasets.

Yujie Shen · Shikun Dong · Jinhui Liu · Liqing Zhang · Jiacheng Zhang · Han Zhou · Weida Dong

BioMed research international · 2020 doi:10.1155/2020/9710421

Paper

complete

Experiment

complete

Data

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Analysis

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Execution

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
id
pmid:32337286
kind
science-record
content_hash
sha256:220fd25e7dabad8f201baaf99d18cac6ee9ebc46f0e71f1efcd90dee95ccbf76
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https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json
created_at
2026-11-01T15:41:00Z
updated_at
2026-11-01T22:01:33Z
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paper object · 10 fields
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complete
title
Identification of Potential Biomarkers for Thyroid Cancer Using Bioinformatics Strategy: A Study Based on GEO Datasets.
doi
10.1155/2020/9710421
pmid
32337286
authors array · 7 items
[0]
Yujie Shen
[1]
Shikun Dong
[2]
Jinhui Liu
[3]
Liqing Zhang
[4]
Jiacheng Zhang
[5]
Han Zhou
[6]
Weida Dong
journal
BioMed research international
year
2020
abstract
BACKGROUND: The molecular mechanisms and genetic markers of thyroid cancer are unclear. In this study, we used bioinformatics to screen for key genes and pathways associated with thyroid cancer development and to reveal its potential molecular mechanisms. METHODS: The GSE3467, GSE3678, GSE33630, and GSE53157 expression profiles downloaded from the Gene Expression Omnibus database (GEO) contained a total of 164 tissue samples (64 normal thyroid tissue samples and 100 thyroid cancer samples). The four datasets were integrated and analyzed by the RobustRankAggreg (RRA) method to obtain differentially expressed genes (DEGs). Using these DEGs, we performed gene ontology (GO) functional annotation, pathway analysis, protein-protein interaction (PPI) analysis and survival analysis. Then, CMap was used to identify the candidate small molecules that might reverse thyroid cancer gene expression. RESULTS: By integrating the four datasets, 330 DEGs, including 154 upregulated and 176 downregulated genes, were identified. GO analysis showed that the upregulated genes were mainly involved in extracellular region, extracellular exosome, and heparin binding. The downregulated genes were mainly concentrated in thyroid hormone generation and proteinaceous extracellular matrix. Pathway analysis showed that the upregulated DEGs were mainly attached to ECM-receptor interaction, p53 signaling pathway, and TGF-beta signaling pathway. Downregulation of DEGs was mainly involved in tyrosine metabolism, mineral absorption, and thyroxine biosynthesis. Among the top 30 hub genes obtained in PPI network, the expression levels of FN1, NMU, CHRDL1, GNAI1, ITGA2, GNA14 and AVPR1A were associated with the prognosis of thyroid cancer. Finally, four small molecules that could reverse the gene expression induced by thyroid cancer, namely ikarugamycin, adrenosterone, hexamethonium bromide and clofazimine, were obtained in the CMap database. CONCLUSION: The identification of the key genes and pathways enhances the understanding of the molecular mechanisms for thyroid cancer. In addition, these key genes may be potential therapeutic targets and biomarkers for the treatment of thyroid cancer.
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The four datasets were integrated and analyzed by the RobustRankAggreg (RRA) method to obtain differentially expressed genes (DEGs).
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sections[0] "Abstract" paragraph 2
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The four datasets were integrated and analyzed by the RobustRankAggreg (RRA) method to obtain differentially expressed genes (DEGs).
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The data used to support the findings of this study are included within the article.
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sections[24] "Data Availability" paragraph 2
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The data used to support the findings of this study are included within the article.
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https://doi.org/10.1155/2020/9710421
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GSM831849
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GSM831850
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GSM831851
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GSM831852
[104]
GSM831853
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105
group_sizes
null
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null
platform
570
taxon
Homo sapiens
title
Normal thyrocytes vs papillary vs anaplastic thyroid carcinomas
resolution_checked_at
2026-11-01T15:39:54Z
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identifier_resolution_only_no_download_no_licence_read
downloaded
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data:geo:GSE3467
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The data used to support the findings of this study are included within the article.
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GSM77374
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GSM77375
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GSM77376
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GSM77378
[17]
GSM77379
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18
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null
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570
taxon
Homo sapiens
title
The role of micro-RNA genes in papillary thyroid carcinoma
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2026-11-01T15:39:54Z
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identifier_resolution_only_no_download_no_licence_read
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The data used to support the findings of this study are included within the article.
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GSM85222
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GSM85223
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GSM85224
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GSM85225
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GSM85226
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GSM85227
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GSM85228
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14
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null
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null
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570
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Homo sapiens
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PTC versus paired normal thyroid tissue
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2026-11-01T15:39:54Z
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identifier_resolution_only_no_download_no_licence_read
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data:geo:GSE53157
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null
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The data used to support the findings of this study are included within the article.
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GSM1283116
[2]
GSM1283117
[3]
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GSM1283121
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GSM1283124
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27
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null
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null
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570
taxon
Homo sapiens
title
Gene expression profiling associated with the progression to poorly differentiated thyroid carcinomas
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2026-11-01T15:39:54Z
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The four datasets were integrated and analyzed by the RobustRankAggreg (RRA) method to obtain differentially expressed genes (DEGs).
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GSE53157
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asset:data:geo:GSE3678 licence not read
[5]
asset:data:geo:GSE3678 not downloaded
[6]
asset:data:geo:GSE53157 licence not read
[7]
asset:data:geo:GSE53157 not downloaded
[8]
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:32337286", "kind": "science-record", "revision": 7, "content_hash": "sha256:220fd25e7dabad8f201baaf99d18cac6ee9ebc46f0e71f1efcd90dee95ccbf76", "created_at": "2026-11-01T15:41:00Z", "updated_at": "2026-11-01T22:01:33Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Identification of Potential Biomarkers for Thyroid Cancer Using Bioinformatics Strategy: A Study Based on GEO Datasets.", "doi": "10.1155/2020/9710421", "pmid": "32337286", "authors": ["Yujie Shen", "Shikun Dong", "Jinhui Liu", "Liqing Zhang", "Jiacheng Zhang", "Han Zhou", "Weida Dong"], "journal": "BioMed research international", "year": 2020, "abstract": "BACKGROUND: The molecular mechanisms and genetic markers of thyroid cancer are unclear. In this study, we used bioinformatics to screen for key genes and pathways associated with thyroid cancer development and to reveal its potential molecular mechanisms.\nMETHODS: The GSE3467, GSE3678, GSE33630, and GSE53157 expression profiles downloaded from the Gene Expression Omnibus database (GEO) contained a total of 164 tissue samples (64 normal thyroid tissue samples and 100 thyroid cancer samples). The four datasets were integrated and analyzed by the RobustRankAggreg (RRA) method to obtain differentially expressed genes (DEGs). Using these DEGs, we performed gene ontology (GO) functional annotation, pathway analysis, protein-protein interaction (PPI) analysis and survival analysis. Then, CMap was used to identify the candidate small molecules that might reverse thyroid cancer gene expression.\nRESULTS: By integrating the four datasets, 330 DEGs, including 154 upregulated and 176 downregulated genes, were identified. GO analysis showed that the upregulated genes were mainly involved in extracellular region, extracellular exosome, and heparin binding. The downregulated genes were mainly concentrated in thyroid hormone generation and proteinaceous extracellular matrix. Pathway analysis showed that the upregulated DEGs were mainly attached to ECM-receptor interaction, p53 signaling pathway, and TGF-beta signaling pathway. Downregulation of DEGs was mainly involved in tyrosine metabolism, mineral absorption, and thyroxine biosynthesis. Among the top 30 hub genes obtained in PPI network, the expression levels of FN1, NMU, CHRDL1, GNAI1, ITGA2, GNA14 and AVPR1A were associated with the prognosis of thyroid cancer. Finally, four small molecules that could reverse the gene expression induced by thyroid cancer, namely ikarugamycin, adrenosterone, hexamethonium bromide and clofazimine, were obtained in the CMap database.\nCONCLUSION: The identification of the key genes and pathways enhances the understanding of the molecular mechanisms for thyroid cancer. In addition, these key genes may be potential therapeutic targets and biomarkers for the treatment of thyroid cancer.", "claims": [{"id": "claim-method", "statement": "The four datasets were integrated and analyzed by the RobustRankAggreg (RRA) method to obtain differentially expressed genes (DEGs).", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:32337286", "locator": "sections[0] \"Abstract\" paragraph 2", "quote": "The four datasets were integrated and analyzed by the RobustRankAggreg (RRA) method to obtain differentially expressed genes (DEGs)."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The data used to support the findings of this study are included within the article.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:32337286", "locator": "sections[24] \"Data Availability\" paragraph 2", "quote": "The data used to support the findings of this study are included within the article."}], "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:32337286"], "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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