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pmid:35606717

Construction and validation of a two-gene signature based on SUMOylation regulatory genes in non-small cell lung cancer patients.

Hongxu Sheng · Zhexue Hao · Linhai Zhu · Yuan Zeng · Jianxing He

BMC cancer · 2022 doi:10.1186/s12885-022-09575-4

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title
Construction and validation of a two-gene signature based on SUMOylation regulatory genes in non-small cell lung cancer patients.
doi
10.1186/s12885-022-09575-4
pmid
35606717
authors array · 5 items
[0]
Hongxu Sheng
[1]
Zhexue Hao
[2]
Linhai Zhu
[3]
Yuan Zeng
[4]
Jianxing He
journal
BMC cancer
year
2022
abstract
BACKGROUND: Post-translational modification plays an important role in the occurrence and development of various tumors. However, few researches were focusing on the SUMOylation regulatory genes as tumor biomarkers to predict the survival for specific patients. Here, we constructed and validated a two-gene signature to predict the overall survival (OS) of non-small cell lung cancer (NSCLC) patients. METHODS: The datasets analyzed in this study were downloaded from TCGA and GEO databases. The least absolute shrinkage and selection operator (LASSO) Cox regression was used to construct the two-gene signature. Gene set enrichment analysis (GSEA) and Gene Ontology (GO) was used to identify hub pathways associated with risk genes. The CCK-8 assay, cell cycle analysis, and transwell assay was used to validate the function of risk genes in NSCLC cell lines. RESULTS: Firstly, most of the SUMOylation regulatory genes were highly expressed in various tumors through the R package 'limma' in the TCGA database. Secondly, our study found that the two gene signature constructed by LASSO regression analysis, as an independent prognostic factor, could predict the OS in both the TCGA training cohort and GEO validation cohorts (GSE68465, GSE37745, and GSE30219). Furthermore, functional enrichment analysis suggests that high-risk patients defined by the risk score system were associated with the malignant phenomenon, such as DNA replication, cell cycle regulation, p53 signaling pathway. Finally, the results of the CCK-8 assay, cell cycle analysis, and transwell assay demonstrated that the two risk genes, SAE1 and UBA2, could promote proliferation and migration in non-small cell lung cancer cells. CONCLUSIONS: The two-gene signature constructed in our study could predict the OS and may provide valuable clinical guidance for the treatment of NSCLC patients.
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The LASSO Cox regression analysis was used in the training set to construct a risk scoring system (RSS) by a linear combination of the risk genes defined by their calculated regression coefficients.
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The LASSO Cox regression analysis was used in the training set to construct a risk scoring system (RSS) by a linear combination of the risk genes defined by their calculated regression coefficients.
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The datasets used in the current study are openly available in TCGA (https://cancergenome.nih.gov/) and GEO (https://www.ncbi.nlm.nih.gov/geo/) database and are available in the scienceDB repository (https://www.scidb.cn/s/AFfEva).
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462
group_sizes
null
group_sizes_basis
null
platform
96
taxon
Homo sapiens
title
caArray_jacob-00182: Gene expression-based survival prediction in lung adenocarcinoma: a multi-site, blinded validation study
resolution_checked_at
2026-11-01T15:39:55Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
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licence_read
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[0]
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asset:data:geo:GSE37745 licence not read
[2]
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[3]
asset:data:geo:GSE68465 licence not read
analysis object · 4 fields
state
complete
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[0] object · 10 fields
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cox_proportional_hazards
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[0]
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[0]
time_to_event_with_censoring
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quote
The LASSO Cox regression analysis was used in the training set to construct a risk scoring system (RSS) by a linear combination of the risk genes defined by their calculated regression coefficients.
[1] object · 10 fields
id
method-2
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differential_expression
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limma_voom
label
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[0]
normalise_counts
[1]
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count_matrix_with_condition
evidence object · 3 fields
score
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quote
limma
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capability object · 3 fields
state
complete
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[0] object · 6 fields
capability_id
capability:computational_analysis
label
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[3]
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[4]
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[6]
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[8]
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candidate
Automated Assays Laravel application and simulated adapters
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readiness object · 8 fields
state
complete
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blocked_on
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tier
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[0]
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.
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tier
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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 object · 6 fields
tier
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accessions array · 3 items
[0]
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[1]
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[2]
and GSE30219
resolved_accessions array · 2 items
[0]
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statements array · 1 item
[0]
The datasets used in the current study are openly available in TCGA (https://cancergenome.nih.gov/) and GEO (https://www.ncbi.nlm.nih.gov/geo/) database and are available in the scienceDB repository (https://www.scidb.cn/s/AFfEva).
basis
The paper names GSE68465, GSE37745 in Gene Expression Omnibus (GEO) and the accession resolves in the repository. No dataset was downloaded and no licence was read.
can_run object · 3 fields
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[0]
cox_ph
assets array · 2 items
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source:pmid:35606717
[1]
data:geo:GSE37745
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[0]
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[0]
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review object · 5 fields
state
partial
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kind
extraction_review
reader object · 5 fields
model
MiniMax-M3.1-Flash
provider
minimax
provider_family
minimax
read_at
2026-11-01T17:47:33Z
independence
single_reader
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method
verbatim
availability
verbatim
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9003
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256
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[0] object · 4 fields
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extraction
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type
paper
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[1] object · 3 fields
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source:pmid:35606717
type
manuscript
label
PMID 35606717 full text
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data:geo:GSE37745
type
dataset
label
GEO GSE37745
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[0] object · 4 fields
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type
classification
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type
paper
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pmid:35606717
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source:pmid:35606717
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PMID 35606717 full text
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data:geo:GSE37745
type
dataset
label
GEO GSE37745
agent
agent:corpus-assay-engine
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extraction
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agent:minimax-reader
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used array · 1 item
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agent:corpus-assay-engine
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sha256:08fa9fa3179f6f486eb5d945aaaf7916a8026b55ec8358bff60038fe0a8e316b
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null
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[0] object · 11 fields
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apoptosis_assay
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evidence array · 2 items
[0]
hub pathways associated with risk genes. The CCK-8 assay, cell cycle analysis, and transwell as
[1]
gnaling pathway. Finally, the results of the CCK-8 assay, cell cycle analysis, and transwell as
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paper_text_order:824
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ell lines and cell culture The A549 and H838 cell lines were cultured in RPMI-1640 medium (Corning, Inc.) suppleme
[1]
ll culture The A549 and H838 cell lines were cultured in RPMI-1640 medium (Corning, Inc.) supplemente
[2]
issing data. Cell lines and cell culture The A549 and H838 cell lines were cultured in RPMI-16
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paper_text_order:2592
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f2132e96ae6c7a4e
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[0]
The LASSO Cox regression analysis was used in the training set to construct a risk scoring system (RSS) by a linear combination of the risk genes defined by their calculated regression coefficients.
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:35606717", "kind": "science-record", "revision": 4, "content_hash": "sha256:064389ff7e8a7b5882cb47ea6a0f4582b2ffe721c02b6a1fcb7369a02a7e01a6", "created_at": "2026-11-01T18:14:31Z", "updated_at": "2026-11-01T22:06:35Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Construction and validation of a two-gene signature based on SUMOylation regulatory genes in non-small cell lung cancer patients.", "doi": "10.1186/s12885-022-09575-4", "pmid": "35606717", "authors": ["Hongxu Sheng", "Zhexue Hao", "Linhai Zhu", "Yuan Zeng", "Jianxing He"], "journal": "BMC cancer", "year": 2022, "abstract": "BACKGROUND: Post-translational modification plays an important role in the occurrence and development of various tumors. However, few researches were focusing on the SUMOylation regulatory genes as tumor biomarkers to predict the survival for specific patients. Here, we constructed and validated a two-gene signature to predict the overall survival (OS) of non-small cell lung cancer (NSCLC) patients.\nMETHODS: The datasets analyzed in this study were downloaded from TCGA and GEO databases. The least absolute shrinkage and selection operator (LASSO) Cox regression was used to construct the two-gene signature. Gene set enrichment analysis (GSEA) and Gene Ontology (GO) was used to identify hub pathways associated with risk genes. The CCK-8 assay, cell cycle analysis, and transwell assay was used to validate the function of risk genes in NSCLC cell lines.\nRESULTS: Firstly, most of the SUMOylation regulatory genes were highly expressed in various tumors through the R package 'limma' in the TCGA database. Secondly, our study found that the two gene signature constructed by LASSO regression analysis, as an independent prognostic factor, could predict the OS in both the TCGA training cohort and GEO validation cohorts (GSE68465, GSE37745, and GSE30219). Furthermore, functional enrichment analysis suggests that high-risk patients defined by the risk score system were associated with the malignant phenomenon, such as DNA replication, cell cycle regulation, p53 signaling pathway. Finally, the results of the CCK-8 assay, cell cycle analysis, and transwell assay demonstrated that the two risk genes, SAE1 and UBA2, could promote proliferation and migration in non-small cell lung cancer cells.\nCONCLUSIONS: The two-gene signature constructed in our study could predict the OS and may provide valuable clinical guidance for the treatment of NSCLC patients.", "claims": [{"id": "claim-method", "statement": "The LASSO Cox regression analysis was used in the training set to construct a risk scoring system (RSS) by a linear combination of the risk genes defined by their calculated regression coefficients.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:35606717", "locator": "sections[6] \"Construction of a risk scoring system\" paragraph 2", "quote": "The LASSO Cox regression analysis was used in the training set to construct a risk scoring system (RSS) by a linear combination of the risk genes defined by their calculated regression coefficients."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The datasets used in the current study are openly available in TCGA (https://cancergenome.nih.gov/) and GEO (https://www.ncbi.nlm.nih.gov/geo/) database and are available in the scienceDB repository (https://www.scidb.cn/s/AFfEva).", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:35606717", "locator": "sections[31] \"notes\" paragraph 1", "quote": "The datasets used in the current study are openly available in TCGA (https://cancergenome.nih.gov/) and GEO (https://www.ncbi.nlm.nih.gov/geo/) database and are available in the scienceDB repository (https://www.scidb.cn/s/AFfEva)."}], "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:35606717"], "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:GSE37745"], "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:GSE37745"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:35606717", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.1186/s12885-022-09575-4", "sha256": 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