Abstract

Background This study is aimed at constructing a risk signature to predict survival outcomes of ORCA patients. Methods We identified differentially expressed autophagy-related genes (DEARGs) based on the RNA sequencing data in the TCGA database; then, four independent survival-related ARGs were identified to construct an autophagy-associated signature for survival prediction of ORCA patients. The validity and robustness of the prognostic model were validated by clinicopathological data and survival data. Subsequently, four independent prognostic DEARGs that composed the model were evaluated individually. Results The expressions of 232 autophagy-related genes (ARGs) in 127 ORCA and 13 control tissues were compared, and 36 DEARGs were filtered out. We performed functional enrichment analysis and constructed protein–protein interaction network for 36 DEARGs. Univariate and multivariate Cox regression analyses were adopted for searching prognostic ARGs, and an autophagy-associated signature for ORCA patients was constructed. Eventually, 4 desirable independent survival-related ARGs (WDR45, MAPK9, VEGFA, and ATIC) were confirmed and comprised the prognostic model. We made use of multiple ways to verify the accuracy of the novel autophagy-related signature for survival evaluation, such as receiver-operator characteristic curve, Kaplan–Meier plotter, and clinicopathological correlational analyses. Four independent prognostic DEARGs that formed the model were also associated with the prognosis of ORCA patients. Conclusions The autophagy-related risk model can evaluate OS for ORCA patients independently since it is accurate and stable. Four prognostic ARGs that composed the model can be studied deeply for target treatment.

Highlights

  • This study is aimed at constructing a risk signature to predict survival outcomes of oral cancer (ORCA) patients

  • The treatment and prognosis of ORCA patients relied on the staging system and conventional prognostic factors used in clinical practice, for example, the tumor-node-metastasis (TNM) staging system was the most important and well-known prognostic factor for ORCA patients [4], but the staging system was not accurate enough and prognostic factors were inadequate and nonspecific, leading to discouraging overall prognosis

  • The risk score model had been verified from several aspects, and we proved its accuracy; we verified the prognosis value of each autophagy-related genes (ARGs) that comprised the autophagy-related risk model and proved them as prognostic biomarkers in ORCA; our report may shed light on evaluating the prognosis and targeting treatment of ORCA

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Summary

Introduction

This study is aimed at constructing a risk signature to predict survival outcomes of ORCA patients. We identified differentially expressed autophagy-related genes (DEARGs) based on the RNA sequencing data in the TCGA database; four independent survival-related ARGs were identified to construct an autophagy-associated signature for survival prediction of ORCA patients. Four independent prognostic DEARGs that composed the model were evaluated individually. We performed functional enrichment analysis and constructed protein– protein interaction network for 36 DEARGs. Univariate and multivariate Cox regression analyses were adopted for searching prognostic ARGs, and an autophagy-associated signature for ORCA patients was constructed. Four independent prognostic DEARGs that formed the model were associated with the prognosis of ORCA patients. The autophagy-related risk model can evaluate OS for ORCA patients independently since it is accurate and stable. This study attempts to refine the prognostic signature of ORCA and used it in the clinical setting

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