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pmid:32462000

Identification and Validation of Prognostically Relevant Gene Signature in Melanoma.

Yali Gao · Yaling Li · Xueli Niu · Yutong Wu · Xiuhao Guan · Yuxiao Hong · Hongduo Chen · Bing Song

BioMed research international · 2020 doi:10.1155/2020/5323614

Paper

complete

Experiment

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Data

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Analysis

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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pmid:32462000
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science-record
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sha256:b6dc304719ee04cafc173e22fa829a4cf174f9cf0abe6916eba42f9e9fd7321e
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2026-11-01T15:41:02Z
updated_at
2026-11-01T22:01:41Z
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paper object · 10 fields
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title
Identification and Validation of Prognostically Relevant Gene Signature in Melanoma.
doi
10.1155/2020/5323614
pmid
32462000
authors array · 8 items
[0]
Yali Gao
[1]
Yaling Li
[2]
Xueli Niu
[3]
Yutong Wu
[4]
Xiuhao Guan
[5]
Yuxiao Hong
[6]
Hongduo Chen
[7]
Bing Song
journal
BioMed research international
year
2020
abstract
BACKGROUND: Currently, effective genetic markers are limited to predict the clinical outcome of melanoma. High-throughput multiomics sequencing data have provided a valuable approach for the identification of genes associated with cancer prognosis. METHOD: The multidimensional data of melanoma patients, including clinical, genomic, and transcriptomic data, were obtained from The Cancer Genome Atlas (TCGA). These samples were then randomly divided into two groups, one for training dataset and the other for validation dataset. In order to select reliable biomarkers, we screened prognosis-related genes, copy number variation genes, and SNP variation genes and integrated these genes to further select features using random forests in the training dataset. We screened for robust biomarkers and established a gene-related prognostic model. Finally, we verified the selected biomarkers in the test sets (GSE19234 and GSE65904) and on clinical samples extracted from melanoma patients using qRT-PCR and immunohistochemistry analysis. RESULTS: We obtained 1569 prognostic-related genes and 1101 copy-amplification, 1093 copy-deletions, and 92 significant mutations in genomic variants. These genomic variant genes were closely related to the development of tumors and genes that integrate genomic variation. A total of 141 candidate genes were obtained from prognosis-related genes. Six characteristic genes (IQCE, RFX6, GPAA1, BAHCC1, CLEC2B, and AGAP2) were selected by random forest feature selection, many of which have been reported to be associated with tumor progression. Cox regression analysis was used to establish a 6-gene signature. Experimental verification with qRT-PCR and immunohistochemical staining proved that these selected genes were indeed expressed at a significantly higher level compared with the normal tissues. This signature comprised an independent prognostic factor for melanoma patients. CONCLUSIONS: We constructed a 6-gene signature (IQCE, RFX6, GPAA1, BAHCC1, CLEC2B, and AGAP2) as a novel prognostic marker for predicting the survival of melanoma patients.
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sections[9] "2.7. Analysis of the Clinical Independence of the 6-Gene Signature Model" paragraph 2
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A univariate and multivariate Cox regression was used to analyze the relevant HR, 95% CI of HR, and p value.
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sections[29] "Data Availability" paragraph 2
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The data used to support the findings of this study are available from the corresponding author upon request.
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Immune profile and mitotic index of metastatic melanoma lesions enhance clinical staging in predicting patient survival.
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Whole-genome expression analysis of melanoma tumor biopsies from a population-based cohort.
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capability_table_fingerprint
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lineage object · 4 fields
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sha256:1c3446ce19825c05a916aaf90741e859d604bfaa2b0c42fc39ca36dbfb80437e
fork_of
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gaps array · 9 items
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asset:data:geo:GSE19234 licence not read
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asset:data:geo:GSE65904 licence not read
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asset:data:geo:GSE65904 not downloaded
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method.reader_differs_from_extractor
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review.human_critique
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review.independent_reader
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review.machine_critique
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assay_lexicon
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confidence
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evidence array · 4 items
[0]
ted from melanoma patients using qRT-PCR and immunohistochemistry analysis. RESULTS: We obtained 1569 prognost
[1]
. Experimental verification with qRT-PCR and immunohistochemical staining proved that these selected genes we
[2]
Biomarker Screening Results with qRT-PCR and Immunohistochemistry Analysis In order to verify whether IQCE, RF
[3]
experimentally confirmed this by qRT-PCR and immunohistochemical staining using melanoma tissues extracted fr
order_basis
paper_text_order:1045
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assay:1
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source_hashes object · 1 field
dsl_catalogue
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evidence array · 1 item
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A univariate and multivariate Cox regression was used to analyze the relevant HR, 95% CI of HR, and p value.
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:32462000", "kind": "science-record", "revision": 7, "content_hash": "sha256:b6dc304719ee04cafc173e22fa829a4cf174f9cf0abe6916eba42f9e9fd7321e", "created_at": "2026-11-01T15:41:02Z", "updated_at": "2026-11-01T22:01:41Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Identification and Validation of Prognostically Relevant Gene Signature in Melanoma.", "doi": "10.1155/2020/5323614", "pmid": "32462000", "authors": ["Yali Gao", "Yaling Li", "Xueli Niu", "Yutong Wu", "Xiuhao Guan", "Yuxiao Hong", "Hongduo Chen", "Bing Song"], "journal": "BioMed research international", "year": 2020, "abstract": "BACKGROUND: Currently, effective genetic markers are limited to predict the clinical outcome of melanoma. High-throughput multiomics sequencing data have provided a valuable approach for the identification of genes associated with cancer prognosis.\nMETHOD: The multidimensional data of melanoma patients, including clinical, genomic, and transcriptomic data, were obtained from The Cancer Genome Atlas (TCGA). These samples were then randomly divided into two groups, one for training dataset and the other for validation dataset. In order to select reliable biomarkers, we screened prognosis-related genes, copy number variation genes, and SNP variation genes and integrated these genes to further select features using random forests in the training dataset. We screened for robust biomarkers and established a gene-related prognostic model. Finally, we verified the selected biomarkers in the test sets (GSE19234 and GSE65904) and on clinical samples extracted from melanoma patients using qRT-PCR and immunohistochemistry analysis.\nRESULTS: We obtained 1569 prognostic-related genes and 1101 copy-amplification, 1093 copy-deletions, and 92 significant mutations in genomic variants. These genomic variant genes were closely related to the development of tumors and genes that integrate genomic variation. A total of 141 candidate genes were obtained from prognosis-related genes. Six characteristic genes (IQCE, RFX6, GPAA1, BAHCC1, CLEC2B, and AGAP2) were selected by random forest feature selection, many of which have been reported to be associated with tumor progression. Cox regression analysis was used to establish a 6-gene signature. Experimental verification with qRT-PCR and immunohistochemical staining proved that these selected genes were indeed expressed at a significantly higher level compared with the normal tissues. This signature comprised an independent prognostic factor for melanoma patients.\nCONCLUSIONS: We constructed a 6-gene signature (IQCE, RFX6, GPAA1, BAHCC1, CLEC2B, and AGAP2) as a novel prognostic marker for predicting the survival of melanoma patients.", "claims": [{"id": "claim-method", "statement": "A univariate and multivariate Cox regression was used to analyze the relevant HR, 95% CI of HR, and p value.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:32462000", "locator": "sections[9] \"2.7. 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This lane did not download the dataset or read its licence.", "duration_hours": null, "parameters": {}, "inputs": ["data:geo:GSE19234"], "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:GSE19234"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:32462000", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.1155/2020/5323614", "sha256": 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