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pmid:32318583

Systems Biology Integration and Screening of Reliable Prognostic Markers to Create Synergies in the Control of Lung Cancer Patients.

Aman Chandra Kaushik · Aamir Mehmood · Dong-Qing Wei · Xiaofeng Dai

Frontiers in molecular biosciences · 2020 doi:10.3389/fmolb.2020.00047

Paper

complete

Experiment

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Data

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Analysis

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title
Systems Biology Integration and Screening of Reliable Prognostic Markers to Create Synergies in the Control of Lung Cancer Patients.
doi
10.3389/fmolb.2020.00047
pmid
32318583
authors array · 4 items
[0]
Aman Chandra Kaushik
[1]
Aamir Mehmood
[2]
Dong-Qing Wei
[3]
Xiaofeng Dai
journal
Frontiers in molecular biosciences
year
2020
abstract
This study aims to achieve a clearer and stronger understanding of all the mechanisms involved in the occurrence as well as in the progression of lung cancer along with discovering trustworthy prognostic markers. We combined four gene expression profiles (GSE19188, GSE19804, GSE101929, and GSE18842) from the GEO database and screened the commonly differentially expressed genes (CDEGs). We performed differentially expressed group analysis on CDEGs, alteration and mutational analysis, and expression level verification of core differential genes. Systems biology discoveries in our examination are predictable with past reports. Curiously, our examination revealed that screened biomarker adjustments, for the most part, coexist in lung cancer. After screening 952 CDEGs, we found that the up-regulation of neuromedin U (NMU) and GTSE1 in the case of lung cancer is related to poor prognosis. On the other hand, FOS CDKN1C expression is associated with poor prognosis and is responsible for the down-regulation of CDKN1C and FOS. Changes in these qualities are on free pathways to lung cancer and are not usually of combined quality variety. Even though biomarkers were related to both survival occasions in our examination, it gives us another point of view while playing out the investigation of hereditary changes and clinical highlights employing information mining. Based on our results, we found potential and prospective clinical applications in GTSE1, NMU, FOS, and CDKN1C to act as prognostic markers in case of lung cancer.
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GSM494675
sample_count
120
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null
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null
platform
570
taxon
Homo sapiens
title
Genome-wide screening of transcriptional modulation in non-smoking female lung cancer in Taiwan
resolution_checked_at
2026-11-01T15:39:54Z
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identifier_resolution_only_no_download_no_licence_read
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[5]
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[6]
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analysis object · 4 fields
state
partial
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null
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score
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“The analysis of prognostic value of CDEGs in the patients who were suffering from lung cancer was done by Kaplan–Meier, with 54,000 genes in 21 tumors.”
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method.reader_named_unmapped
capability object · 3 fields
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candidate
Automated Assays Laravel application and simulated adapters
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method
blocked_on
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basis
The reader quoted the method the paper names (Kaplan–Meier survival analysis), but the corpus's method extractor could not map it onto a DSL operation, so the method is published but not expressible.
capability object · 4 fields
tier
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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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GSE19188
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statements array · 1 item
[0]
The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation, to any qualified researcher.
basis
The paper names GSE19188, GSE19804, GSE101929, GSE18842 in GEO database and the accession resolves in the repository. No dataset was downloaded and no licence was read.
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review object · 5 fields
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independence
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data:geo:GSE101929
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dataset
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GEO GSE101929
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classification
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PMID 32318583 full text
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dataset
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GEO GSE101929
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agent:corpus-assay-engine
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agent:minimax-reader
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Complete file
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We combined four gene expression profiles (GSE19188, GSE19804, GSE101929, and GSE18842) from the GEO database and screened the commonly differentially expressed genes (CDEGs). We performed differentially expressed group analysis on CDEGs, alteration and mutational analysis, and expression level verification of core differential genes. Systems biology discoveries in our examination are predictable with past reports. Curiously, our examination revealed that screened biomarker adjustments, for the most part, coexist in lung cancer. After screening 952 CDEGs, we found that the up-regulation of neuromedin U (NMU) and GTSE1 in the case of lung cancer is related to poor prognosis. On the other hand, FOS CDKN1C expression is associated with poor prognosis and is responsible for the down-regulation of CDKN1C and FOS. Changes in these qualities are on free pathways to lung cancer and are not usually of combined quality variety. Even though biomarkers were related to both survival occasions in our examination, it gives us another point of view while playing out the investigation of hereditary changes and clinical highlights employing information mining. 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