Gene signature predicting recurrence in oral squamous cell carcinoma is characterized by increased oxidative phosphorylation

Although numerous studies have used systemic approaches to identify prognostic predictors in oral squamous cell carcinoma (OSCC), the effectiveness of these approaches has not been assessed clinically. Further, the mechanism underlying malignant behaviors in OSCC is poorly characterized. This study...

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Main Authors: Joo Kyung Noh, Seon Rang Woo, Moonkyoo Kong, Min Kyeong Lee, Jung Woo Lee, Young Chan Lee, Seong‐Gyu Ko, Young‐Gyu Eun
Format: Article
Language:English
Published: Wiley 2023-01-01
Series:Molecular Oncology
Subjects:
Online Access:https://doi.org/10.1002/1878-0261.13328
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author Joo Kyung Noh
Seon Rang Woo
Moonkyoo Kong
Min Kyeong Lee
Jung Woo Lee
Young Chan Lee
Seong‐Gyu Ko
Young‐Gyu Eun
author_facet Joo Kyung Noh
Seon Rang Woo
Moonkyoo Kong
Min Kyeong Lee
Jung Woo Lee
Young Chan Lee
Seong‐Gyu Ko
Young‐Gyu Eun
author_sort Joo Kyung Noh
collection DOAJ
description Although numerous studies have used systemic approaches to identify prognostic predictors in oral squamous cell carcinoma (OSCC), the effectiveness of these approaches has not been assessed clinically. Further, the mechanism underlying malignant behaviors in OSCC is poorly characterized. This study aimed to develop and verify accurate prognostic predictors for OSCC patients and assess the associated biology. We identified an OSCC‐recurrence‐related gene signature (ORGS) using a Cox regression analysis. Functional enrichment analysis was used to identify enriched pathways and biological processes to reveal the underlying mechanism of OSCC malignant behavior. The ORGS successfully divided OSCC patients into low‐ and high‐risk groups with significantly different overall survivals. Pathway analysis revealed oxidative phosphorylation (OXPHOS) as a signaling pathway associated with the ORGS in OSCC. Interestingly, high OXPHOS status was strongly associated with poor overall survival in OSCC patients. Mediator complex subunit 30 (MED30) was a predicted upstream regulator of OXPHOS, and knockdown of MED30 reduced histone acetylation. We identified that the ORGS was strongly correlated with OXPHOS regulatory processes, suggesting OXPHOS as a key mechanism leading to poor prognosis in OSCC.
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spelling doaj.art-44ec1059df5b4e028e6ad23be021ce592023-01-05T03:41:34ZengWileyMolecular Oncology1574-78911878-02612023-01-0117113414910.1002/1878-0261.13328Gene signature predicting recurrence in oral squamous cell carcinoma is characterized by increased oxidative phosphorylationJoo Kyung Noh0Seon Rang Woo1Moonkyoo Kong2Min Kyeong Lee3Jung Woo Lee4Young Chan Lee5Seong‐Gyu Ko6Young‐Gyu Eun7Department of Biomedical Science and Technology, Graduate School Kyung Hee University Seoul KoreaDepartment of Otolaryngology‐Head & Neck Surgery, Kyung Hee University School of Medicine Kyung Hee University Medical Center Seoul KoreaDepartment of Radiation Oncology, Kyung Hee University School of Medicine Kyung Hee University Medical Center Seoul KoreaDepartment of Biomedical Science and Technology, Graduate School Kyung Hee University Seoul KoreaDepartment of Oral and Maxillofacial Surgery, School of Dentistry Kyung Hee University Seoul KoreaDepartment of Otolaryngology‐Head & Neck Surgery, Kyung Hee University School of Medicine Kyung Hee University Medical Center Seoul KoreaDepartment of Preventive Medicine, College of Korean Medicine Kyung Hee University Seoul KoreaDepartment of Biomedical Science and Technology, Graduate School Kyung Hee University Seoul KoreaAlthough numerous studies have used systemic approaches to identify prognostic predictors in oral squamous cell carcinoma (OSCC), the effectiveness of these approaches has not been assessed clinically. Further, the mechanism underlying malignant behaviors in OSCC is poorly characterized. This study aimed to develop and verify accurate prognostic predictors for OSCC patients and assess the associated biology. We identified an OSCC‐recurrence‐related gene signature (ORGS) using a Cox regression analysis. Functional enrichment analysis was used to identify enriched pathways and biological processes to reveal the underlying mechanism of OSCC malignant behavior. The ORGS successfully divided OSCC patients into low‐ and high‐risk groups with significantly different overall survivals. Pathway analysis revealed oxidative phosphorylation (OXPHOS) as a signaling pathway associated with the ORGS in OSCC. Interestingly, high OXPHOS status was strongly associated with poor overall survival in OSCC patients. Mediator complex subunit 30 (MED30) was a predicted upstream regulator of OXPHOS, and knockdown of MED30 reduced histone acetylation. We identified that the ORGS was strongly correlated with OXPHOS regulatory processes, suggesting OXPHOS as a key mechanism leading to poor prognosis in OSCC.https://doi.org/10.1002/1878-0261.13328gene signatureMED30mitochondrial membrane potentialoral squamous cell carcinomaoxidative phosphorylation
spellingShingle Joo Kyung Noh
Seon Rang Woo
Moonkyoo Kong
Min Kyeong Lee
Jung Woo Lee
Young Chan Lee
Seong‐Gyu Ko
Young‐Gyu Eun
Gene signature predicting recurrence in oral squamous cell carcinoma is characterized by increased oxidative phosphorylation
Molecular Oncology
gene signature
MED30
mitochondrial membrane potential
oral squamous cell carcinoma
oxidative phosphorylation
title Gene signature predicting recurrence in oral squamous cell carcinoma is characterized by increased oxidative phosphorylation
title_full Gene signature predicting recurrence in oral squamous cell carcinoma is characterized by increased oxidative phosphorylation
title_fullStr Gene signature predicting recurrence in oral squamous cell carcinoma is characterized by increased oxidative phosphorylation
title_full_unstemmed Gene signature predicting recurrence in oral squamous cell carcinoma is characterized by increased oxidative phosphorylation
title_short Gene signature predicting recurrence in oral squamous cell carcinoma is characterized by increased oxidative phosphorylation
title_sort gene signature predicting recurrence in oral squamous cell carcinoma is characterized by increased oxidative phosphorylation
topic gene signature
MED30
mitochondrial membrane potential
oral squamous cell carcinoma
oxidative phosphorylation
url https://doi.org/10.1002/1878-0261.13328
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