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Significant Biomarkers Identification Associated with Cutaneous Squamous Cell Carcinoma Progression

BACKGROUND: This study aimed to identify significant genes associated with cutaneous squamous cell carcinoma (CSCC) initiation and development. METHODS: The overlapped differential expressed genes (DEGs) between normal and CSCC samples were firstly screened out, followed by KEGG analysis. The top 10...

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Autores principales: Qiu, Cheng-Gang, Shen, Bin, Sun, Xiao-Qi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8901050/
https://www.ncbi.nlm.nih.gov/pubmed/35264873
http://dx.doi.org/10.2147/IJGM.S357022
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author Qiu, Cheng-Gang
Shen, Bin
Sun, Xiao-Qi
author_facet Qiu, Cheng-Gang
Shen, Bin
Sun, Xiao-Qi
author_sort Qiu, Cheng-Gang
collection PubMed
description BACKGROUND: This study aimed to identify significant genes associated with cutaneous squamous cell carcinoma (CSCC) initiation and development. METHODS: The overlapped differential expressed genes (DEGs) between normal and CSCC samples were firstly screened out, followed by KEGG analysis. The top 10 hub genes were then detected from the whole protein–protein interaction (PPI) network. Further, important biomarkers continuously associated with actinic keratosis (AK), CSCC, and CSCC invasion was successively filtrated. GSEA analysis was finally performed to reveal potential mechanisms associated with biomarkers. RESULTS: A total of 179 DEGs were identified, which were enriched in pathways in cancer, PI3K-Akt signaling pathway, and human papillomavirus infection. The 10 hub genes were firstly identified from the PPI network, and they were all highly expressed in AK tissues compared with normal tissues. Next, we found that 6 genes were overexpressed in CSCC compared with AK tissues. Further, we identified that the expression of 2 genes (MYBL2 and TK1) was higher in CSCC invasion groups compared with samples without invasion. Through a series of filtrations, we confirmed that MYBL2 and TK1 were the most significant biomarkers associated with CSCC initiation and progression. The pan-cancer analysis further supported their prognostic value in human cancers. GSEA analysis found that they positively correlated with N glycan biosynthesis and p53 signaling pathways. CONCLUSION: MYBL2 and TK1 were proved to play a vital role in CSCC tumorigenesis and progression, which may act as promising biomarkers or therapeutic targets for accurate diagnosis and treatment of CSCC.
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spelling pubmed-89010502022-03-08 Significant Biomarkers Identification Associated with Cutaneous Squamous Cell Carcinoma Progression Qiu, Cheng-Gang Shen, Bin Sun, Xiao-Qi Int J Gen Med Original Research BACKGROUND: This study aimed to identify significant genes associated with cutaneous squamous cell carcinoma (CSCC) initiation and development. METHODS: The overlapped differential expressed genes (DEGs) between normal and CSCC samples were firstly screened out, followed by KEGG analysis. The top 10 hub genes were then detected from the whole protein–protein interaction (PPI) network. Further, important biomarkers continuously associated with actinic keratosis (AK), CSCC, and CSCC invasion was successively filtrated. GSEA analysis was finally performed to reveal potential mechanisms associated with biomarkers. RESULTS: A total of 179 DEGs were identified, which were enriched in pathways in cancer, PI3K-Akt signaling pathway, and human papillomavirus infection. The 10 hub genes were firstly identified from the PPI network, and they were all highly expressed in AK tissues compared with normal tissues. Next, we found that 6 genes were overexpressed in CSCC compared with AK tissues. Further, we identified that the expression of 2 genes (MYBL2 and TK1) was higher in CSCC invasion groups compared with samples without invasion. Through a series of filtrations, we confirmed that MYBL2 and TK1 were the most significant biomarkers associated with CSCC initiation and progression. The pan-cancer analysis further supported their prognostic value in human cancers. GSEA analysis found that they positively correlated with N glycan biosynthesis and p53 signaling pathways. CONCLUSION: MYBL2 and TK1 were proved to play a vital role in CSCC tumorigenesis and progression, which may act as promising biomarkers or therapeutic targets for accurate diagnosis and treatment of CSCC. Dove 2022-03-02 /pmc/articles/PMC8901050/ /pubmed/35264873 http://dx.doi.org/10.2147/IJGM.S357022 Text en © 2022 Qiu et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Qiu, Cheng-Gang
Shen, Bin
Sun, Xiao-Qi
Significant Biomarkers Identification Associated with Cutaneous Squamous Cell Carcinoma Progression
title Significant Biomarkers Identification Associated with Cutaneous Squamous Cell Carcinoma Progression
title_full Significant Biomarkers Identification Associated with Cutaneous Squamous Cell Carcinoma Progression
title_fullStr Significant Biomarkers Identification Associated with Cutaneous Squamous Cell Carcinoma Progression
title_full_unstemmed Significant Biomarkers Identification Associated with Cutaneous Squamous Cell Carcinoma Progression
title_short Significant Biomarkers Identification Associated with Cutaneous Squamous Cell Carcinoma Progression
title_sort significant biomarkers identification associated with cutaneous squamous cell carcinoma progression
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8901050/
https://www.ncbi.nlm.nih.gov/pubmed/35264873
http://dx.doi.org/10.2147/IJGM.S357022
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