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Identification of novel prognostic indicators for oral squamous cell carcinoma based on proteomics and metabolomics

BACKGROUND: The low 5-year survival rate of oral squamous cell carcinoma (OSCC) suggests that new prognostic indicators need to be identified to aid the clinical management of patients. METHODS: Saliva samples from OSCC patients and healthy controls were collected for proteomic and metabolomic seque...

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Autores principales: Yao, Zhitao, An, Wei, Tuerdi, Maimaitituxun, Zhao, Jin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Neoplasia Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10172993/
https://www.ncbi.nlm.nih.gov/pubmed/37084685
http://dx.doi.org/10.1016/j.tranon.2023.101672
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author Yao, Zhitao
An, Wei
Tuerdi, Maimaitituxun
Zhao, Jin
author_facet Yao, Zhitao
An, Wei
Tuerdi, Maimaitituxun
Zhao, Jin
author_sort Yao, Zhitao
collection PubMed
description BACKGROUND: The low 5-year survival rate of oral squamous cell carcinoma (OSCC) suggests that new prognostic indicators need to be identified to aid the clinical management of patients. METHODS: Saliva samples from OSCC patients and healthy controls were collected for proteomic and metabolomic sequencing. Gene expressed profiling was downloaded from TCGA and GEO databases. After the differential analysis, proteins with a significant impact on the prognosis of OSCC patients were screened. Correlation analysis was performed with metabolites and core proteins were identified. Cox regression analysis was utilized to stratify OSCC samples based on core proteins. The prognostic predictive ability of the core protein was then evaluated. Differences in infiltration of immune cells between the different strata were identified. RESULTS: There were 678 differentially expressed proteins (DEPs), 94 intersected DEPs among them by intersecting with differentially expressed genes in TCGA and GSE30784 dataset. Seven core proteins were identified that significantly affected OSCC patient survival and strongly correlated with differential metabolites (R(2) > 0.8). The samples were divided into high- and low-risk groups according to median risk score. The risk score and core proteins were well prognostic factor in OSCC patients. Genes in high-risk group were enriched in Notch signaling pathway, epithelial mesenchymal transition (EMT), and angiogenesis. Core proteins were strongly associated with the immune status of OSCC patients. CONCLUSIONS: The results established a 7-protein signatures with the hope of early detection and the capacity for risk assessment of OSCC patient prognosis. Further providing more potential targets for the treatment of OSCC.
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spelling pubmed-101729932023-05-12 Identification of novel prognostic indicators for oral squamous cell carcinoma based on proteomics and metabolomics Yao, Zhitao An, Wei Tuerdi, Maimaitituxun Zhao, Jin Transl Oncol Original Research BACKGROUND: The low 5-year survival rate of oral squamous cell carcinoma (OSCC) suggests that new prognostic indicators need to be identified to aid the clinical management of patients. METHODS: Saliva samples from OSCC patients and healthy controls were collected for proteomic and metabolomic sequencing. Gene expressed profiling was downloaded from TCGA and GEO databases. After the differential analysis, proteins with a significant impact on the prognosis of OSCC patients were screened. Correlation analysis was performed with metabolites and core proteins were identified. Cox regression analysis was utilized to stratify OSCC samples based on core proteins. The prognostic predictive ability of the core protein was then evaluated. Differences in infiltration of immune cells between the different strata were identified. RESULTS: There were 678 differentially expressed proteins (DEPs), 94 intersected DEPs among them by intersecting with differentially expressed genes in TCGA and GSE30784 dataset. Seven core proteins were identified that significantly affected OSCC patient survival and strongly correlated with differential metabolites (R(2) > 0.8). The samples were divided into high- and low-risk groups according to median risk score. The risk score and core proteins were well prognostic factor in OSCC patients. Genes in high-risk group were enriched in Notch signaling pathway, epithelial mesenchymal transition (EMT), and angiogenesis. Core proteins were strongly associated with the immune status of OSCC patients. CONCLUSIONS: The results established a 7-protein signatures with the hope of early detection and the capacity for risk assessment of OSCC patient prognosis. Further providing more potential targets for the treatment of OSCC. Neoplasia Press 2023-04-20 /pmc/articles/PMC10172993/ /pubmed/37084685 http://dx.doi.org/10.1016/j.tranon.2023.101672 Text en © 2023 The Authors. Published by Elsevier Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Research
Yao, Zhitao
An, Wei
Tuerdi, Maimaitituxun
Zhao, Jin
Identification of novel prognostic indicators for oral squamous cell carcinoma based on proteomics and metabolomics
title Identification of novel prognostic indicators for oral squamous cell carcinoma based on proteomics and metabolomics
title_full Identification of novel prognostic indicators for oral squamous cell carcinoma based on proteomics and metabolomics
title_fullStr Identification of novel prognostic indicators for oral squamous cell carcinoma based on proteomics and metabolomics
title_full_unstemmed Identification of novel prognostic indicators for oral squamous cell carcinoma based on proteomics and metabolomics
title_short Identification of novel prognostic indicators for oral squamous cell carcinoma based on proteomics and metabolomics
title_sort identification of novel prognostic indicators for oral squamous cell carcinoma based on proteomics and metabolomics
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10172993/
https://www.ncbi.nlm.nih.gov/pubmed/37084685
http://dx.doi.org/10.1016/j.tranon.2023.101672
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