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Uses of Vascular Endothelial Growth Factor C as a Lung Adenocarcinoma Prognostic Biomarker
BACKGROUND: Lung adenocarcinoma (LUAD) is the most common type of lung cancer and a leading cause of death worldwide. Vascular endothelial growth factor C (VEGF-C) has been identified as a prognosis prediction marker for LUAD. However, VEGF-C protein expression does not appear to significantly relat...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elmer Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9990733/ https://www.ncbi.nlm.nih.gov/pubmed/36896001 http://dx.doi.org/10.14740/wjon1520 |
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author | Chen, Shi Pan, Ting Yu Wu, Xiao Li, Tian Wei, Yu He, Hai Lang Zhou, Xian Mei Wang, Qian Zhu, Ji Ping |
author_facet | Chen, Shi Pan, Ting Yu Wu, Xiao Li, Tian Wei, Yu He, Hai Lang Zhou, Xian Mei Wang, Qian Zhu, Ji Ping |
author_sort | Chen, Shi |
collection | PubMed |
description | BACKGROUND: Lung adenocarcinoma (LUAD) is the most common type of lung cancer and a leading cause of death worldwide. Vascular endothelial growth factor C (VEGF-C) has been identified as a prognosis prediction marker for LUAD. However, VEGF-C protein expression does not appear to significantly relate to LUAD patient survival in several studies. METHODS: We carried out a bioinformatic analysis to review the effect of VEGF-C mRNA expression on LUAD patient outcomes. GEPIA, UALCAN, TCGAportal, OncoLnc, LCE, GeneMANIA, Metascape, ImmuCellAI, and GSCA online databases were utilized. The expression levels of VEGF-C mRNA between normal tissue and LUAD tissue, overall survival (OS) analysis, function analysis, tumor microenvironment and drug sensitivity were conducted in the current study. RESULTS: We found that the expression level of VEGF-C mRNA was significantly lower in LUAD than normal tissue. Low expression of VEGF-C mRNA was also associated with better OS. VEGF-C expression was correlated with both NF1 and TP53 mutation status. No relationship was observed between VEGF-C and Tr1 or CD4 T-cell infiltrate scores. Additionally, VEGF-C was associated with epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor resistance. The sensitivity of 5-fluorouracil was positively correlated with VEGF-C, and the sensitivity of TGX221 was negatively correlated with VEGF-C. The activity of BI-2536 and BRD-A94377914 was positively correlated with VEGF-C. CONCLUSION: Novel LUAD prognostic biomarkers such as VEGF-C mRNA may aid diagnosis and treatment, and may help identify optimal LUAD populations for therapeutic treatments. |
format | Online Article Text |
id | pubmed-9990733 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elmer Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-99907332023-03-08 Uses of Vascular Endothelial Growth Factor C as a Lung Adenocarcinoma Prognostic Biomarker Chen, Shi Pan, Ting Yu Wu, Xiao Li, Tian Wei, Yu He, Hai Lang Zhou, Xian Mei Wang, Qian Zhu, Ji Ping World J Oncol Original Article BACKGROUND: Lung adenocarcinoma (LUAD) is the most common type of lung cancer and a leading cause of death worldwide. Vascular endothelial growth factor C (VEGF-C) has been identified as a prognosis prediction marker for LUAD. However, VEGF-C protein expression does not appear to significantly relate to LUAD patient survival in several studies. METHODS: We carried out a bioinformatic analysis to review the effect of VEGF-C mRNA expression on LUAD patient outcomes. GEPIA, UALCAN, TCGAportal, OncoLnc, LCE, GeneMANIA, Metascape, ImmuCellAI, and GSCA online databases were utilized. The expression levels of VEGF-C mRNA between normal tissue and LUAD tissue, overall survival (OS) analysis, function analysis, tumor microenvironment and drug sensitivity were conducted in the current study. RESULTS: We found that the expression level of VEGF-C mRNA was significantly lower in LUAD than normal tissue. Low expression of VEGF-C mRNA was also associated with better OS. VEGF-C expression was correlated with both NF1 and TP53 mutation status. No relationship was observed between VEGF-C and Tr1 or CD4 T-cell infiltrate scores. Additionally, VEGF-C was associated with epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor resistance. The sensitivity of 5-fluorouracil was positively correlated with VEGF-C, and the sensitivity of TGX221 was negatively correlated with VEGF-C. The activity of BI-2536 and BRD-A94377914 was positively correlated with VEGF-C. CONCLUSION: Novel LUAD prognostic biomarkers such as VEGF-C mRNA may aid diagnosis and treatment, and may help identify optimal LUAD populations for therapeutic treatments. Elmer Press 2023-02 2023-02-26 /pmc/articles/PMC9990733/ /pubmed/36896001 http://dx.doi.org/10.14740/wjon1520 Text en Copyright 2023, Chen et al. https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution Non-Commercial 4.0 International License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Chen, Shi Pan, Ting Yu Wu, Xiao Li, Tian Wei, Yu He, Hai Lang Zhou, Xian Mei Wang, Qian Zhu, Ji Ping Uses of Vascular Endothelial Growth Factor C as a Lung Adenocarcinoma Prognostic Biomarker |
title | Uses of Vascular Endothelial Growth Factor C as a Lung Adenocarcinoma Prognostic Biomarker |
title_full | Uses of Vascular Endothelial Growth Factor C as a Lung Adenocarcinoma Prognostic Biomarker |
title_fullStr | Uses of Vascular Endothelial Growth Factor C as a Lung Adenocarcinoma Prognostic Biomarker |
title_full_unstemmed | Uses of Vascular Endothelial Growth Factor C as a Lung Adenocarcinoma Prognostic Biomarker |
title_short | Uses of Vascular Endothelial Growth Factor C as a Lung Adenocarcinoma Prognostic Biomarker |
title_sort | uses of vascular endothelial growth factor c as a lung adenocarcinoma prognostic biomarker |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9990733/ https://www.ncbi.nlm.nih.gov/pubmed/36896001 http://dx.doi.org/10.14740/wjon1520 |
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