Evidence map›Paper›PMID 36849997›Full record

ArticleBMC medical genomics2023

Identification of gene profiles related to the development of oral cancer using a deep learning technique.

Leili Tapak, Mohammad Kazem Ghasemi, Saeid Afshar, Hossein Mahjub, Alireza Soltanian, Hassan Khotanlou

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Article in BMC medical genomics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

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0cells of the map it votes in
5citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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5 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Leili TapakDepartment of Biostatistics, School of Public Health and Modeling of Noncommunicable Diseases Research Center, Hamadan University of Medical Sciences, Hamadan, Iran.
Mohammad Kazem GhasemiDepartment of Biostatistics, School of Public Health, Hamadan University of Medical Sciences, Hamadan, Iran.
Saeid AfsharResearch Center for Molecular Medicine, Hamadan University of Medical Sciences, Hamadan, Iran. s.afshar@umsha.ac.ir.
Hossein MahjubDepartment of Biostatistics, School of Public Health and Modeling of Noncommunicable Diseases Research Center, Hamadan University of Medical Sciences, Hamadan, Iran.
Alireza SoltanianDepartment of Biostatistics, School of Public Health and Modeling of Noncommunicable Diseases Research Center, Hamadan University of Medical Sciences, Hamadan, Iran.
Hassan KhotanlouDepartment of Computer Engineering, Bu-Ali Sina University, Hamadan, Iran.

Funding

Hamadan University of Medical Sciences 9807305722
6 · The paper itself

Abstract

backgroundOral cancer (OC) is a debilitating disease that can affect the quality of life of these patients adversely. Oral premalignant lesion patients have a high risk of developing OC. Therefore, identifying robust survival subgroups among them may significantly improve patient therapy and care. This study aimed to identify prognostic biomarkers that predict the time-to-development of OC and survival stratification for patients using state-of-the-art machine learning and deep learning.

methodsGene expression profiles (29,096 probes) related to 86 patients from the GSE26549 dataset from the GEO repository were used. An autoencoder deep learning neural network model was used to extract features. We also used a univariate Cox regression model to select significant features obtained from the deep learning method (P < 0.05). High-risk and low-risk groups were then identified using a hierarchical clustering technique based on 100 encoded features (the number of units of the encoding layer, i.e., bottleneck of the network) from autoencoder and selected by Cox proportional hazards model and a supervised random forest (RF) classifier was used to identify gene profiles related to subtypes of OC from the original 29,096 probes.

resultsAmong 100 encoded features extracted by autoencoder, seventy features were significantly related to time-to-OC-development, based on the univariate Cox model, which was used as the inputs for the clustering of patients. Two survival risk groups were identified (P value of log-rank test = 0.003) and were used as the labels for supervised classification. The overall accuracy of the RF classifier was 0.916 over the test set, yielded 21 top genes (FUT8-DDR2-ATM-CD247-ETS1-ZEB2-COL5A2-GMAP7-CDH1-COL11A2-COL3A1-AHR-COL2A1-CHORDC1-PTP4A3-COL1A2-CCR2-PDGFRB-COL1A1-FERMT2-PIK3CB) associated with time to developing OC, selected among the original 29,096 probes.

conclusionsUsing deep learning, our study identified prominent transcriptional biomarkers in determining high-risk patients for developing oral cancer, which may be prognostic as significant targets for OC therapy. The identified genes may serve as potential targets for oral cancer chemoprevention. Additional validation of these biomarkers in experimental prospective and retrospective studies will launch them in OC clinics.

Indexed as

Deep LearningMouth NeoplasmsCollagen Type IHumansNeoplasm ProteinsProspective StudiesProtein Tyrosine PhosphatasesQuality of LifeRetrospective StudiesCollagen Type ICollagen Type I, alpha2 SubunitNeoplasm ProteinsProtein Tyrosine PhosphatasesPTP4A3 protein, humanDeep learningGene expressionOral cancer

Identifiers

PMID36849997
PMCPMC9972685

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