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pmid:35058964

Comprehensive Analysis to Identify SPP1 as a Prognostic Biomarker in Cervical Cancer.

Kaidi Zhao · Zhou Ma · Wei Zhang

Frontiers in genetics · 2021 doi:10.3389/fgene.2021.732822

Paper

complete

Experiment

partial

Data

partial

Analysis

partial

Execution

absent

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title
Comprehensive Analysis to Identify SPP1 as a Prognostic Biomarker in Cervical Cancer.
doi
10.3389/fgene.2021.732822
pmid
35058964
authors array · 3 items
[0]
Kaidi Zhao
[1]
Zhou Ma
[2]
Wei Zhang
journal
Frontiers in genetics
year
2021
abstract
Background: SPP1, secreted phosphoprotein 1, is a member of the small integrin-binding ligand N-linked glycoprotein (SIBLING) family. Previous studies have proven SPP1 overexpressed in a variety of cancers and can be identified as a prognostic factor, while no study has explored the function and carcinogenic mechanism of SPP1 in cervical cancer. Methods: We aimed to demonstrate the relationship between SPP1 expression and pan-cancer using The Cancer Genome Atlas (TCGA) database. Next, we validated SPP1 expression of cervical cancer in the Gene Expression Omnibus (GEO) database, including GSE7803, GSE63514, and GSE9750. The receiver operating characteristic (ROC) curve was used to evaluate the feasibility of SPP1 as a differentiating factor by the area under curve (AUC) score. Cox regression and logistic regression were performed to evaluate factors associated with prognosis. The SPP1-binding protein network was built by the STRING tool. Enrichment analysis by the R package clusterProfiler was used to explore potential function of SPP1. The single-sample GSEA (ssGSEA) method from the R package GSVA and TIMER database were used to investigate the association between the immune infiltration level and SPP1 expression in cervical cancer. Results: Pan-cancer data analysis showed that SPP1 expression was higher in most cancer types, including cervical cancer, and we got the same result in the GEO database. The ROC curve suggested that SPP1 could be a potential diagnostic biomarker (AUC = 0.877). High SPP1 expression was associated with poorer overall survival (OS) (P = 0.032). Further enrichment and immune infiltration analysis revealed that high SPP1 expression was correlated with regulating the infiltration level of neutrophil cells and some immune cell types, including macrophage and DC. Conclusion: SPP1 expression was higher in cervical cancer tissues than in normal cervical epithelial tissues. It was significantly associated with poor prognosis and immune cell infiltration. Thus, SPP1 may become a promising prognostic biomarker for cervical cancer patients.
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We performed univariate and multivariate Cox analyses of overall survival (OS) in cervical cancer patients, and results are shown in Table 3.
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sections[10] "Association Between SPP1 Expression and Cancer Patient Survival Prognosis" paragraph 2
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We performed univariate and multivariate Cox analyses of overall survival (OS) in cervical cancer patients, and results are shown in Table 3.
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Publicly available datasets were analyzed in this study. These data can be found freely from TCGA data portal (https://portal.gdc.cancer.gov/) and GEO database (https://www.ncbi.nlm.nih.gov/geo/).
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sections[15] "Data Availability Statement" paragraph 2
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Publicly available datasets were analyzed in this study. These data can be found freely from TCGA data portal (https://portal.gdc.cancer.gov/) and GEO database (https://www.ncbi.nlm.nih.gov/geo/).
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Higher SPP1 mRNA expression was associated with poorer overall survival in cervical cancer patients.
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According to the KM plot, patients with higher SPP1 mRNA expression showed poorer prognosis than the lower group (HR = 1.69, 95% CI: 1.05–2.72, P = 0.032) (Figure 3).
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sections[10] "Association Between SPP1 Expression and Cancer Patient Survival Prognosis" paragraph 2
quote
According to the KM plot, patients with higher SPP1 mRNA expression showed poorer prognosis than the lower group (HR = 1.69, 95% CI: 1.05–2.72, P = 0.032) (Figure 3).
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Higher SPP1 mRNA expression was associated with poorer overall survival in cervical cancer patients.
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Gene expression analysis of cervical cancer progression
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Identification of gene expression profiles in cervical cancer
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:35058964", "kind": "science-record", "revision": 4, "content_hash": "sha256:f0c40a98e9fd84f7d5e0d4ccc91c3b3571ba5fb1cccbe672d9fd3499a70ff999", "created_at": "2026-11-01T17:36:47Z", "updated_at": "2026-11-01T22:05:38Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Comprehensive Analysis to Identify SPP1 as a Prognostic Biomarker in Cervical Cancer.", "doi": "10.3389/fgene.2021.732822", "pmid": "35058964", "authors": ["Kaidi Zhao", "Zhou Ma", "Wei Zhang"], "journal": "Frontiers in genetics", "year": 2021, "abstract": "Background: SPP1, secreted phosphoprotein 1, is a member of the small integrin-binding ligand N-linked glycoprotein (SIBLING) family. Previous studies have proven SPP1 overexpressed in a variety of cancers and can be identified as a prognostic factor, while no study has explored the function and carcinogenic mechanism of SPP1 in cervical cancer. Methods: We aimed to demonstrate the relationship between SPP1 expression and pan-cancer using The Cancer Genome Atlas (TCGA) database. Next, we validated SPP1 expression of cervical cancer in the Gene Expression Omnibus (GEO) database, including GSE7803, GSE63514, and GSE9750. The receiver operating characteristic (ROC) curve was used to evaluate the feasibility of SPP1 as a differentiating factor by the area under curve (AUC) score. Cox regression and logistic regression were performed to evaluate factors associated with prognosis. The SPP1-binding protein network was built by the STRING tool. Enrichment analysis by the R package clusterProfiler was used to explore potential function of SPP1. The single-sample GSEA (ssGSEA) method from the R package GSVA and TIMER database were used to investigate the association between the immune infiltration level and SPP1 expression in cervical cancer. Results: Pan-cancer data analysis showed that SPP1 expression was higher in most cancer types, including cervical cancer, and we got the same result in the GEO database. The ROC curve suggested that SPP1 could be a potential diagnostic biomarker (AUC = 0.877). High SPP1 expression was associated with poorer overall survival (OS) (P = 0.032). Further enrichment and immune infiltration analysis revealed that high SPP1 expression was correlated with regulating the infiltration level of neutrophil cells and some immune cell types, including macrophage and DC. Conclusion: SPP1 expression was higher in cervical cancer tissues than in normal cervical epithelial tissues. It was significantly associated with poor prognosis and immune cell infiltration. Thus, SPP1 may become a promising prognostic biomarker for cervical cancer patients.", "claims": [{"id": "claim-method", "statement": "We performed univariate and multivariate Cox analyses of overall survival (OS) in cervical cancer patients, and results are shown in Table 3.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:35058964", "locator": "sections[10] \"Association Between SPP1 Expression and Cancer Patient Survival Prognosis\" paragraph 2", "quote": "We performed univariate and multivariate Cox analyses of overall survival (OS) in cervical cancer patients, and results are shown in Table 3."}], "state": "complete"}, {"id": "claim-data-access", "statement": "Publicly available datasets were analyzed in this study. These data can be found freely from TCGA data portal (https://portal.gdc.cancer.gov/) and GEO database (https://www.ncbi.nlm.nih.gov/geo/).", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:35058964", "locator": "sections[15] \"Data Availability Statement\" paragraph 2", "quote": "Publicly available datasets were analyzed in this study. These data can be found freely from TCGA data portal (https://portal.gdc.cancer.gov/) and GEO database (https://www.ncbi.nlm.nih.gov/geo/)."}], "state": "complete"}, {"id": "claim-target-result", "statement": "Higher SPP1 mRNA expression was associated with poorer overall survival in cervical cancer patients.", "kind": "quantitative", "target": {"value": 95.0, "unit": "per cent", "tolerance": null, "source": "According to the KM plot, patients with higher SPP1 mRNA expression showed poorer prognosis than the lower group (HR = 1.69, 95% CI: 1.05–2.72, P = 0.032) (Figure 3)."}, "evidence": [{"asset": "source:pmid:35058964", "locator": "sections[10] \"Association Between SPP1 Expression and Cancer Patient Survival Prognosis\" paragraph 2", "quote": "According to the KM plot, patients with higher SPP1 mRNA expression showed poorer prognosis than the lower group (HR = 1.69, 95% CI: 1.05–2.72, P = 0.032) (Figure 3)."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "partial", "objective": "Higher SPP1 mRNA expression was associated with poorer overall survival in cervical cancer patients.", "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:35058964"], "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:GSE63514"], "outputs": ["the source data with its repository provenance"], "instruments": [], "reagents": []}, {"id": "run_analysis", "order": 3, "name": "Run the published analysis", "kind": "analysis", "state": "blocked", "blocked_on": "method:group_comparison_wilcoxon", "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:GSE63514"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": ["step:run_analysis blocked on method:group_comparison_wilcoxon"]}, "data": {"state": "partial", "assets": [{"id": "source:pmid:35058964", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.3389/fgene.2021.732822", "sha256": "sha256:cae18afb95f93f8229b409003bc18464bc2437409878125335476727948eca2a", "bytes": 24337, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "10.3389/fgene.2021.732822", "version": null, "note": "Full article fetched from PMC; the checksum covers the rendered section body, not the original XML bytes.", "structure": {"pmcid": "PMC8764398", "source": "europe_pmc_fulltext", "coverage": "whole_body_without_references", "text_hash_scope": "rendered_section_body"}}, {"id": "data:geo:GSE63514", "role": "raw", "format": "geo-series", "media_type": "application/vnd.ncbi.geo-series+json", "uri": "https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE63514", "sha256": null, "bytes": null, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "GSE63514", "version": null, "note": "Publicly available datasets were analyzed in this study. These data can be found freely from TCGA data portal (https://portal.gdc.cancer.gov/) and GEO database (https://www.ncbi.nlm.nih.gov/geo/).", "structure": {"repository": "GEO", "access_route": "GEO accession URL", "access_statement_verbatim": "Publicly available datasets were analyzed in this study. 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