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pmid:36295640

Anti-CXCL8 Autoantibody: A Potential Diagnostic Biomarker for Esophageal Squamous Cell Carcinoma.

Huili Chen · Guiying Sun · Zhuo Han · Huimin Wang · Jiaxin Li · Hua Ye · Chunhua Song · Jianying Zhang · Peng Wang

Medicina (Kaunas, Lithuania) · 2022 doi:10.3390/medicina58101480

Paper

complete

Experiment

complete

Data

partial

Analysis

partial

Execution

absent

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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pmid:36295640
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title
Anti-CXCL8 Autoantibody: A Potential Diagnostic Biomarker for Esophageal Squamous Cell Carcinoma.
doi
10.3390/medicina58101480
pmid
36295640
authors array · 9 items
[0]
Huili Chen
[1]
Guiying Sun
[2]
Zhuo Han
[3]
Huimin Wang
[4]
Jiaxin Li
[5]
Hua Ye
[6]
Chunhua Song
[7]
Jianying Zhang
[8]
Peng Wang
journal
Medicina (Kaunas, Lithuania)
year
2022
abstract
Background and Objectives: Esophageal squamous cell carcinoma (ESCC) is one of the most common malignancies. Anti-tumor associated antigen autoantibodies (TAAbs) can be used as biomarkers for tumor detection. The aim of this study was to identify a reliable TAAb as the diagnostic marker for ESCC. Materials and Methods: The Cancer Genome Atlas (TCGA) database was used to screen candidate genes. The mRNA expression of the key gene was then verified by micro array dataset GSE44021 from the Gene Expression Omnibus (GEO) database and the diag nostic value of the corresponding autoantibody to the key gene in ESCC was detected by enzyme-linked im muno sorbent assay (ELISA). Results: CXCL8 was identified as the key gene. The dataset GSE44021 showed that CXCL8 mRNA expression was prominently over-expressed in ESCC tissues compared with normal tissues. ELISA results showed that the level of anti-CXCL8 autoantibody in ESCC patients was significantly higher than in normal controls and the receiver operating char ac teristic (ROC) curve indicated that anti-CXCL8 autoantibody could discriminate ESCC patients from normal controls, with the area under the ROC curve (AUC) for the verification cohort, and the validation cohort were 0.713 and 0.751, respectively. Conclusions: Our study illustrated that anti-CXCL8 autoantibody had good diagnostic value, and may become a candidate biomarker for ESCC.
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The differences in expression levels of autoantibodies between ESCC patients and normal controls were compared by using the nonparametric test. Receiver operating characteristic (ROC) curves were used to assess the diagnostic ability of anti-CXCL8 autoantibody. Meanwhile, Youden’s index, likelihood ratio, and predictive value were calculated to evaluate the ability of anti-CXCL8 autoantibody to differentiate ESCC patients from normal controls. The area under the ROC curve (AUC) values of different clinical subgroups were analyzed by DeLong test. The frequency of anti-CXCL8 autoantibody in clinical subgroups was analyzed by chi-square test.
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The differences in expression levels of autoantibodies between ESCC patients and normal controls were compared by using the nonparametric test. Receiver operating characteristic (ROC) curves were used to assess the diagnostic ability of anti-CXCL8 autoantibody. Meanwhile, Youden’s index, likelihood ratio, and predictive value were calculated to evaluate the ability of anti-CXCL8 autoantibody to differentiate ESCC patients from normal controls. The area under the ROC curve (AUC) values of different clinical subgroups were analyzed by DeLong test. The frequency of anti-CXCL8 autoantibody in clinical subgroups was analyzed by chi-square test.
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The analyzed data sets generated during the study are available from the corresponding author on reasonable request for noncommercial use.
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Anti-CXCL8 autoantibody discriminates ESCC patients from normal controls, with AUC values of 0.713 and 0.751 in the verification and validation cohorts, respectively.
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ELISA results showed that the level of anti-CXCL8 autoantibody in ESCC patients was significantly higher than in normal controls and the receiver operating char ac teristic (ROC) curve indicated that anti-CXCL8 autoantibody could discriminate ESCC patients from normal controls, with the area under the ROC curve (AUC) for the verification cohort, and the validation cohort were 0.713 and 0.751, respectively.
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Anti-CXCL8 autoantibody discriminates ESCC patients from normal controls, with AUC values of 0.713 and 0.751 in the verification and validation cohorts, respectively.
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Intergrated analysis of array-miRNAs and matched Affymetrix gene
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The differences in expression levels of autoantibodies between ESCC patients and normal controls were compared by using the nonparametric test. Receiver operating characteristic (ROC) curves were used to assess the diagnostic ability of anti-CXCL8 autoantibody. Meanwhile, Youden’s index, likelihood ratio, and predictive value were calculated to evaluate the ability of anti-CXCL8 autoantibody to differentiate ESCC patients from normal controls. The area under the ROC curve (AUC) values of different clinical subgroups were analyzed by DeLong test. The frequency of anti-CXCL8 autoantibody in clinical subgroups was analyzed by chi-square test.
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cted by enzyme-linked im muno sorbent assay (ELISA). Results: CXCL8 was identified as the key g
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f2132e96ae6c7a4e
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The differences in expression levels of autoantibodies between ESCC patients and normal controls were compared by using the nonparametric test. Receiver operating characteristic (ROC) curves were used to assess the diagnostic ability of anti-CXCL8 autoantibody. Meanwhile, Youden’s index, likelihood ratio, and predictive value were calculated to evaluate the ability of anti-CXCL8 autoantibody to differentiate ESCC patients from normal controls. The area under the ROC curve (AUC) values of different clinical subgroups were analyzed by DeLong test. The frequency of anti-CXCL8 autoantibody in clinical subgroups was analyzed by chi-square test.
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{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:36295640", "kind": "science-record", "revision": 4, "content_hash": "sha256:cf8d32175dcfd21a1ad5c3cc4598f7acdd2ae955ce5d52f596c6efa2e002f39a", "created_at": "2026-11-01T18:15:42Z", "updated_at": "2026-11-01T22:07:57Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Anti-CXCL8 Autoantibody: A Potential Diagnostic Biomarker for Esophageal Squamous Cell Carcinoma.", "doi": "10.3390/medicina58101480", "pmid": "36295640", "authors": ["Huili Chen", "Guiying Sun", "Zhuo Han", "Huimin Wang", "Jiaxin Li", "Hua Ye", "Chunhua Song", "Jianying Zhang", "Peng Wang"], "journal": "Medicina (Kaunas, Lithuania)", "year": 2022, "abstract": "Background and Objectives: Esophageal squamous cell carcinoma (ESCC) is one of the most common malignancies. Anti-tumor associated antigen autoantibodies (TAAbs) can be used as biomarkers for tumor detection. The aim of this study was to identify a reliable TAAb as the diagnostic marker for ESCC. Materials and Methods: The Cancer Genome Atlas (TCGA) database was used to screen candidate genes. The mRNA expression of the key gene was then verified by micro array dataset GSE44021 from the Gene Expression Omnibus (GEO) database and the diag nostic value of the corresponding autoantibody to the key gene in ESCC was detected by enzyme-linked im muno sorbent assay (ELISA). Results: CXCL8 was identified as the key gene. The dataset GSE44021 showed that CXCL8 mRNA expression was prominently over-expressed in ESCC tissues compared with normal tissues. ELISA results showed that the level of anti-CXCL8 autoantibody in ESCC patients was significantly higher than in normal controls and the receiver operating char ac teristic (ROC) curve indicated that anti-CXCL8 autoantibody could discriminate ESCC patients from normal controls, with the area under the ROC curve (AUC) for the verification cohort, and the validation cohort were 0.713 and 0.751, respectively. Conclusions: Our study illustrated that anti-CXCL8 autoantibody had good diagnostic value, and may become a candidate biomarker for ESCC.", "claims": [{"id": "claim-method", "statement": "The differences in expression levels of autoantibodies between ESCC patients and normal controls were compared by using the nonparametric test. Receiver operating characteristic (ROC) curves were used to assess the diagnostic ability of anti-CXCL8 autoantibody. Meanwhile, Youden’s index, likelihood ratio, and predictive value were calculated to evaluate the ability of anti-CXCL8 autoantibody to differentiate ESCC patients from normal controls. The area under the ROC curve (AUC) values of different clinical subgroups were analyzed by DeLong test. The frequency of anti-CXCL8 autoantibody in clinical subgroups was analyzed by chi-square test.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:36295640", "locator": "sections[8] \"2.6. Statistical Analysis\" paragraph 2", "quote": "The differences in expression levels of autoantibodies between ESCC patients and normal controls were compared by using the nonparametric test. Receiver operating characteristic (ROC) curves were used to assess the diagnostic ability of anti-CXCL8 autoantibody. Meanwhile, Youden’s index, likelihood ratio, and predictive value were calculated to evaluate the ability of anti-CXCL8 autoantibody to differentiate ESCC patients from normal controls. The area under the ROC curve (AUC) values of different clinical subgroups were analyzed by DeLong test. 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This lane did not download the dataset or read its licence.", "duration_hours": null, "parameters": {}, "inputs": ["data:geo:GSE44021"], "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:GSE44021"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:36295640", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.3390/medicina58101480", "sha256": 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