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pmid:37304542

Prognostic model construction and immune microenvironment analysis of esophageal cancer based on gene expression data and microRNA target genes.

Bingbing Gu · Shuai Zhang · Zhe Fan · Jiajing Che · Shuting Li · Yunfei Li · Keyu Pan · Jiali Lv · Cheng Wang · Tao Zhang · Jialin Wang

Translational cancer research · 2023 doi:10.21037/tcr-22-2588

Paper

complete

Experiment

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Data

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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pmid:37304542
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2026-11-01T19:02:02Z
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2026-11-01T22:09:40Z
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title
Prognostic model construction and immune microenvironment analysis of esophageal cancer based on gene expression data and microRNA target genes.
doi
10.21037/tcr-22-2588
pmid
37304542
authors array · 11 items
[0]
Bingbing Gu
[1]
Shuai Zhang
[2]
Zhe Fan
[3]
Jiajing Che
[4]
Shuting Li
[5]
Yunfei Li
[6]
Keyu Pan
[7]
Jiali Lv
[8]
Cheng Wang
[9]
Tao Zhang
[10]
Jialin Wang
journal
Translational cancer research
year
2023
abstract
Background: Accumulating evidence suggests that microRNA-target genes are closely related to tumorigenesis and progression. This study aims to screen the intersection of differentially expressed mRNAs (DEmRNAs) and the target genes of differentially expressed microRNAs (DEmiRNAs), and to construct a prognostic gene model of esophageal cancer (EC). Methods: Gene expression, microRNA expression, somatic mutation, and clinical information data of EC from The Cancer Genome Atlas (TCGA) database were used. The intersection of DEmRNAs and the target genes of DEmiRNAs predicted by the Targetscan database and microRNA Data Integration Portal (mirDIP) database were screened. The screened genes were used to construct a prognostic model of EC. Then, the molecular and immune signatures of these genes were explored. Finally, the GSE53625 dataset from the Gene Expression Omnibus (GEO) database was further used as a validation cohort to confirm the prognostic value of the genes. Results: Six genes on the grounds of the intersection of DEmiRNAs target genes and DEmRNAs were identified as prognostic genes, including ARHGAP11A, H1.4, HMGB3, LRIG1, PRR11, and COL4A1. Based on the median risk score calculated for these genes, EC patients were divided into a high-risk group (n=72) and a low-risk group (n=72). Survival analysis showed that the high-risk group had a significantly shorter survival time than the low-risk group (TCGA and GEO, P<0.001). The nomogram evaluation showed high reliability in predicting the 1-year, 2-year, and 3-year survival probability of EC patients. Compared to low-risk group, higher expression level of M2 macrophages was found in high-risk group of EC patient (P<0.05), while STAT3 checkpoints showed attenuated expression level in high-risk group. Conclusions: A panel of differential genes was identified as potential EC prognostic biomarkers and showed great clinical significance in EC prognosis.
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Least absolute shrinkage and selection operator (LASSO) Cox regression analysis was used to select differential genes to construct final prognostic model using the R package “glmnet” (13). Then, Cox regression analysis was performed to construct the best prognostic model and make proportional hazards assumption with R package “survival” and “MASS”.
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Least absolute shrinkage and selection operator (LASSO) Cox regression analysis was used to select differential genes to construct final prognostic model using the R package “glmnet” (13). Then, Cox regression analysis was performed to construct the best prognostic model and make proportional hazards assumption with R package “survival” and “MASS”.
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Gene expression, microRNA expression, somatic mutation, and clinical information data of EC from The Cancer Genome Atlas (TCGA) database were used.
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Survival analysis showed that the high-risk group had a significantly shorter survival time than the low-risk group (TCGA and GEO, P<0.001).
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Survival analysis showed that the high-risk group had a significantly shorter survival time than the low-risk group (TCGA and GEO, P<0.001).
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readiness object · 8 fields
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method object · 5 fields
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required_operations array · 1 item
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cox_ph
missing_operations array · 0 items
basis
The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: cox_proportional_hazards.
capability object · 4 fields
tier
R1
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capability:computational_analysis
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basis
The computational analysis is owned. The physical bench the paper used is not, so a physical validation cannot be run here.
data object · 6 fields
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GSE53625
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GSE53625
statements array · 1 item
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Gene expression, microRNA expression, somatic mutation, and clinical information data of EC from The Cancer Genome Atlas (TCGA) database were used.
basis
The paper names GSE53625 in Gene Expression Omnibus (GEO) and the accession resolves in the repository. No dataset was downloaded and no licence was read.
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cox_ph
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data:geo:GSE53625
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review object · 5 fields
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MiniMax-M3.1-Flash
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2026-11-01T18:43:39Z
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pmid:37304542
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paper
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pmid:37304542
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source:pmid:37304542
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manuscript
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PMID 37304542 full text
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data:geo:GSE53625
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GEO GSE53625
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activity-reading-sci-2026-11-01
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classification
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pmid:37304542
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source:pmid:37304542
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PMID 37304542 full text
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data:geo:GSE53625
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dataset
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GEO GSE53625
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agent:corpus-assay-engine
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activity-read-37304542
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extraction
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agent:minimax-reader
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activity-resolve-GSE53625
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accession_resolution
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agent:corpus-assay-engine
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Corpus assay engine
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lineage object · 4 fields
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sha256:89454db11ea74e2a2d0d1c8c0bda43fa6e32a33927a874160fbf35739615913c
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gaps array · 7 items
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asset:data:geo:GSE53625 licence not read
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review.machine_critique
assays array · 1 item
[0] object · 11 fields
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dsl_catalogue
f2132e96ae6c7a4e
evidence array · 1 item
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Least absolute shrinkage and selection operator (LASSO) Cox regression analysis was used to select differential genes to construct final prognostic model using the R package “glmnet” (13). Then, Cox regression analysis was performed to construct the best prognostic model and make proportional hazards assumption with R package “survival” and “MASS”.
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:37304542", "kind": "science-record", "revision": 3, "content_hash": "sha256:880f78a79520f9e957968f22b00ea72167ca47c5960264cdf31f0f05b28eb0f4", "created_at": "2026-11-01T19:02:02Z", "updated_at": "2026-11-01T22:09:40Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Prognostic model construction and immune microenvironment analysis of esophageal cancer based on gene expression data and microRNA target genes.", "doi": "10.21037/tcr-22-2588", "pmid": "37304542", "authors": ["Bingbing Gu", "Shuai Zhang", "Zhe Fan", "Jiajing Che", "Shuting Li", "Yunfei Li", "Keyu Pan", "Jiali Lv", "Cheng Wang", "Tao Zhang", "Jialin Wang"], "journal": "Translational cancer research", "year": 2023, "abstract": "Background: Accumulating evidence suggests that microRNA-target genes are closely related to tumorigenesis and progression. This study aims to screen the intersection of differentially expressed mRNAs (DEmRNAs) and the target genes of differentially expressed microRNAs (DEmiRNAs), and to construct a prognostic gene model of esophageal cancer (EC).\nMethods: Gene expression, microRNA expression, somatic mutation, and clinical information data of EC from The Cancer Genome Atlas (TCGA) database were used. The intersection of DEmRNAs and the target genes of DEmiRNAs predicted by the Targetscan database and microRNA Data Integration Portal (mirDIP) database were screened. The screened genes were used to construct a prognostic model of EC. Then, the molecular and immune signatures of these genes were explored. Finally, the GSE53625 dataset from the Gene Expression Omnibus (GEO) database was further used as a validation cohort to confirm the prognostic value of the genes.\nResults: Six genes on the grounds of the intersection of DEmiRNAs target genes and DEmRNAs were identified as prognostic genes, including ARHGAP11A, H1.4, HMGB3, LRIG1, PRR11, and COL4A1. Based on the median risk score calculated for these genes, EC patients were divided into a high-risk group (n=72) and a low-risk group (n=72). Survival analysis showed that the high-risk group had a significantly shorter survival time than the low-risk group (TCGA and GEO, P<0.001). The nomogram evaluation showed high reliability in predicting the 1-year, 2-year, and 3-year survival probability of EC patients. Compared to low-risk group, higher expression level of M2 macrophages was found in high-risk group of EC patient (P<0.05), while STAT3 checkpoints showed attenuated expression level in high-risk group.\nConclusions: A panel of differential genes was identified as potential EC prognostic biomarkers and showed great clinical significance in EC prognosis.", "claims": [{"id": "claim-method", "statement": "Least absolute shrinkage and selection operator (LASSO) Cox regression analysis was used to select differential genes to construct final prognostic model using the R package “glmnet” (13). Then, Cox regression analysis was performed to construct the best prognostic model and make proportional hazards assumption with R package “survival” and “MASS”.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:37304542", "locator": "sections[5] \"Construction and validation of a prognostic model\" paragraph 2", "quote": "Least absolute shrinkage and selection operator (LASSO) Cox regression analysis was used to select differential genes to construct final prognostic model using the R package “glmnet” (13). Then, Cox regression analysis was performed to construct the best prognostic model and make proportional hazards assumption with R package “survival” and “MASS”."}], "state": "complete"}, {"id": "claim-data-access", "statement": "Gene expression, microRNA expression, somatic mutation, and clinical information data of EC from The Cancer Genome Atlas (TCGA) database were used.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:37304542", "locator": "sections[0] \"Abstract\" paragraph 2", "quote": "Gene expression, microRNA expression, somatic mutation, and clinical information data of EC from The Cancer Genome Atlas (TCGA) database were used."}], "state": "complete"}, {"id": "claim-target-result", "statement": "Survival analysis showed that the high-risk group had a significantly shorter survival time than the low-risk group (TCGA and GEO, P<0.001).", "kind": "quantitative", "target": {"value": 0.001, "unit": "p-value", "tolerance": null, "source": "Survival analysis showed that the high-risk group had a significantly shorter survival time than the low-risk group (TCGA and GEO, P<0.001)."}, "evidence": [{"asset": "source:pmid:37304542", "locator": "sections[0] \"Abstract\" paragraph 3", "quote": "Survival analysis showed that the high-risk group had a significantly shorter survival time than the low-risk group (TCGA and GEO, P<0.001)."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "Survival analysis showed that the high-risk group had a significantly shorter survival time than the low-risk group (TCGA and GEO, P<0.001).", "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:37304542"], "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:GSE53625"], "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:GSE53625"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:37304542", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.21037/tcr-22-2588", "sha256": 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Atlas (TCGA) database were used.", "structure": {"repository": "GEO", "access_route": "GEO accession URL", "access_statement_verbatim": "Gene expression, microRNA expression, somatic mutation, and clinical information data of EC from The Cancer Genome Atlas (TCGA) database were used.", "access_statement_kind": "repository_route_statement", "sample_accessions": ["GSM1296956", "GSM1296957", "GSM1296958", "GSM1296959", "GSM1296960", "GSM1296961", "GSM1296962", "GSM1296963", "GSM1296964", "GSM1296965", "GSM1296966", "GSM1296967", "GSM1296968", "GSM1296969", "GSM1296970", "GSM1296971", "GSM1296972", "GSM1296973", "GSM1296974", "GSM1296975", "GSM1296976", "GSM1296977", "GSM1296978", "GSM1296979", "GSM1296980", "GSM1296981", "GSM1296982", "GSM1296983", "GSM1296984", "GSM1296985", "GSM1296986", "GSM1296987", "GSM1296988", "GSM1296989", "GSM1296990", "GSM1296991", "GSM1296992", "GSM1296993", "GSM1296994", "GSM1296995", "GSM1296996", "GSM1296997", "GSM1296998", "GSM1296999", "GSM1297000", 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"family": "survival_analysis", "specific": "cox_proportional_hazards", "label": "Survival analysis", "dsl_operations": ["cox_ph"], "missing_operations": [], "expressible": true, "parameters": {}, "data_shapes": ["time_to_event_with_censoring"], "evidence": {"score": 1.0, "band": "verbatim", "quote": "Least absolute shrinkage and selection operator (LASSO) Cox regression analysis was used to select differential genes to construct final prognostic model using the R package “glmnet” (13). Then, Cox regression analysis was performed to construct the best prognostic model and make proportional hazards assumption with R package “survival” and “MASS”."}}, {"id": "method-2", "family": "group_comparison", "specific": "mann_whitney", "label": "Group comparison", "dsl_operations": [], "missing_operations": ["group_comparison_mann_whitney"], "expressible": false, "parameters": {}, "data_shapes": ["two_or_more_groups_continuous"], "evidence": {"score": 0.8, "band": "high", "quote": "Mann-Whitney"}}, {"id": "method-3", "family": "group_comparison", "specific": "wilcoxon", "label": "Group comparison", "dsl_operations": [], "missing_operations": ["group_comparison_wilcoxon"], "expressible": false, "parameters": {}, "data_shapes": ["two_or_more_groups_continuous"], "evidence": {"score": 0.8, "band": "high", "quote": "Wilcoxon"}}, {"id": "method-4", "family": "contingency_analysis", "specific": "chi_square", "label": "Categorical (contingency table) analysis", "dsl_operations": ["chi_square_test"], "missing_operations": [], "expressible": true, "parameters": {}, "data_shapes": ["categorical_cross_tabulation"], "evidence": {"score": 0.8, "band": "high", "quote": "χ2"}}], "targets": [{"id": "target-published-estimate", "claim_id": "claim-target-result", "operation": "chi_square_test", "expected_value": 0.001, "unit": "p-value", "tolerance": null, "state": "complete", "note": "The threshold the paper applied to its own result, as the paper states it. A run that reproduces the effect is judged against this threshold."}], "gaps": ["method.reader_differs_from_extractor"]}, "capability": {"state": "complete", "requirements": [{"capability_id": "capability:computational_analysis", "label": "Computational analysis platform", "assay_families": ["meta_analysis", "machine_learning", "survival_analysis", "statistical_regression", "pca", "molecular_docking", "network_analysis", "differential_expression", "gwas"], "availability_state": "owned", "tier_unlocked": "R1", "candidate": "Automated Assays Laravel application and simulated adapters"}], "gaps": []}, "readiness": {"state": "complete", "tier": "R1", "blocking_axis": "none", "blocked_on": "nothing:replicable_now", "axes": {"method": {"tier": "R1", "expressible": true, "required_operations": ["cox_ph"], "missing_operations": [], "basis": "The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: cox_proportional_hazards."}, "capability": {"tier": "R1", "capability_id": "capability:computational_analysis", "availability_state": "owned", "basis": "The computational analysis is owned. The physical bench the paper used is not, so a physical validation cannot be run here."}, "data": {"tier": "R1", "reachable": true, "accessions": ["GSE53625"], "resolved_accessions": ["GSE53625"], "statements": ["Gene expression, microRNA expression, somatic mutation, and clinical information data of EC from The Cancer Genome Atlas (TCGA) database were used."], "basis": "The paper names GSE53625 in Gene Expression Omnibus (GEO) and the accession resolves in the repository. 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