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pmid:33519887

RNA Sequencing Reveals LINC00167 as a Potential Diagnosis Biomarker for Primary Osteoarthritis: A Multi-Stage Study.

Liying Jiang · Yiqin Zhou · Junjie Shen · Yi Chen · Ziyuan Ma · Yuhui Yu · Minjie Chu · Qirong Qian · Xun Zhuang · Shengli Xia

Frontiers in genetics · 2020 doi:10.3389/fgene.2020.539489

Paper

complete

Experiment

complete

Data

partial

Analysis

partial

Execution

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title
RNA Sequencing Reveals LINC00167 as a Potential Diagnosis Biomarker for Primary Osteoarthritis: A Multi-Stage Study.
doi
10.3389/fgene.2020.539489
pmid
33519887
authors array · 10 items
[0]
Liying Jiang
[1]
Yiqin Zhou
[2]
Junjie Shen
[3]
Yi Chen
[4]
Ziyuan Ma
[5]
Yuhui Yu
[6]
Minjie Chu
[7]
Qirong Qian
[8]
Xun Zhuang
[9]
Shengli Xia
journal
Frontiers in genetics
year
2020
abstract
OBJECTIVES: Given the roles played by lncRNA in human diseases and the high incidence of OA, this study investigated the pivotal pathways involved in the disease and identified potential biomarkers for OA diagnosis. METHODS: We first performed an exploration of RNA-sequencing in peripheral blood leukocytes from six subjects (3 OA and 3 healthy controls). Promising candidate lncRNAs were evaluated in first stage validation using a GEO dataset (GSE114007) of 38 subjects (20 OA and 18 healthy controls), followed by a second stage validation using quantitative PCR analysis with 101 subjects (67 OA and 34 controls). The third stage investigated the potential value of validated lncRNA in the early diagnosis of OA in peripheral blood leukocytes from a total of 120 participants (60 cases and 60 controls). RESULTS: The dataset identified a total of 1,380 up-regulated and 719 down-regulated mRNAs and 5,743 up-regulated and 7,384 down-regulated lncRNAs. The up-regulated DEGs were mainly enriched in the extracellular matrix, while the down-regulated DEGs were mainly enriched in the IL-17 and wnt signaling pathways. 18 overlapping candidate lncRNAs survived after first-stage validation. 3 hub lncRNAs were selected for the second validation stage and qualified in an external sample, and lncRNA LINC00167 was further confirmed with a similar result (down-expressed in both stages). Receiver operating characteristic analysis showed that LINC00167 can distinguish OA cases from healthy controls with a high area under the curve of 0.879 (95%CI: 0.819, 0.938; P < 0.001), with a sensitivity of 80.7% and specificity of 83.5%. CONCLUSION: The expression profile of OA was identified and critical pathways were elucidated by an integrated approach to RNA-seq from easily accessible blood. LINC00167 may serve as a potential early diagnosis marker for OA in clinical practice. The detailed mechanism of action of this lncRNA requires further elucidation in future studies.
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To investigate the potential value in OA diagnosis, the ROC curve was calculated using subjects from the third stage validation, including 60 OA cases and 60 healthy controls.
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sections[13] "Evaluation of Hub-lncRNA for OA Diagnosis" paragraph 2
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To investigate the potential value in OA diagnosis, the ROC curve was calculated using subjects from the third stage validation, including 60 OA cases and 60 healthy controls.
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This manuscript contains previously unpublished data. The name of the repository is GEO and accession number is GSE163552.
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Identification of transcription factors responsible for dysregulated networks in human osteoarthritis cartilage by global gene expression analysis
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Next Generation Sequencing Facilitates Quantitative Analysis of Osteoarthritis related long non-coding RNAs (LcnRNAs)
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Association Between the Serum Levels of LINC0067 and Clinical Characteristics of OA Patients
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RNA Sequencing Reveals LINC00167 as a Potential Diagnosis B
[1]
ETHODS: We first performed an exploration of RNA-sequencing in peripheral blood leukocytes from six subj
[2]
were elucidated by an integrated approach to RNA-seq from easily accessible blood. LINC00167 may
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:33519887", "kind": "science-record", "revision": 7, "content_hash": "sha256:9a112d0958f1b1ef9674dd490054a1c52f75961223ce0618cb431a2808786d87", "created_at": "2026-11-01T15:41:23Z", "updated_at": "2026-11-01T22:03:00Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "RNA Sequencing Reveals LINC00167 as a Potential Diagnosis Biomarker for Primary Osteoarthritis: A Multi-Stage Study.", "doi": "10.3389/fgene.2020.539489", "pmid": "33519887", "authors": ["Liying Jiang", "Yiqin Zhou", "Junjie Shen", "Yi Chen", "Ziyuan Ma", "Yuhui Yu", "Minjie Chu", "Qirong Qian", "Xun Zhuang", "Shengli Xia"], "journal": "Frontiers in genetics", "year": 2020, "abstract": "OBJECTIVES: Given the roles played by lncRNA in human diseases and the high incidence of OA, this study investigated the pivotal pathways involved in the disease and identified potential biomarkers for OA diagnosis.\nMETHODS: We first performed an exploration of RNA-sequencing in peripheral blood leukocytes from six subjects (3 OA and 3 healthy controls). Promising candidate lncRNAs were evaluated in first stage validation using a GEO dataset (GSE114007) of 38 subjects (20 OA and 18 healthy controls), followed by a second stage validation using quantitative PCR analysis with 101 subjects (67 OA and 34 controls). The third stage investigated the potential value of validated lncRNA in the early diagnosis of OA in peripheral blood leukocytes from a total of 120 participants (60 cases and 60 controls).\nRESULTS: The dataset identified a total of 1,380 up-regulated and 719 down-regulated mRNAs and 5,743 up-regulated and 7,384 down-regulated lncRNAs. The up-regulated DEGs were mainly enriched in the extracellular matrix, while the down-regulated DEGs were mainly enriched in the IL-17 and wnt signaling pathways. 18 overlapping candidate lncRNAs survived after first-stage validation. 3 hub lncRNAs were selected for the second validation stage and qualified in an external sample, and lncRNA LINC00167 was further confirmed with a similar result (down-expressed in both stages). Receiver operating characteristic analysis showed that LINC00167 can distinguish OA cases from healthy controls with a high area under the curve of 0.879 (95%CI: 0.819, 0.938; P < 0.001), with a sensitivity of 80.7% and specificity of 83.5%.\nCONCLUSION: The expression profile of OA was identified and critical pathways were elucidated by an integrated approach to RNA-seq from easily accessible blood. LINC00167 may serve as a potential early diagnosis marker for OA in clinical practice. The detailed mechanism of action of this lncRNA requires further elucidation in future studies.", "claims": [{"id": "claim-method", "statement": "To investigate the potential value in OA diagnosis, the ROC curve was calculated using subjects from the third stage validation, including 60 OA cases and 60 healthy controls.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:33519887", "locator": "sections[13] \"Evaluation of Hub-lncRNA for OA Diagnosis\" paragraph 2", "quote": "To investigate the potential value in OA diagnosis, the ROC curve was calculated using subjects from the third stage validation, including 60 OA cases and 60 healthy controls."}], "state": "complete"}, {"id": "claim-data-access", "statement": "This manuscript contains previously unpublished data. 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