Multi-Omics Analyses to Identify FCGBP as a Potential Predictor in Head and Neck Squamous Cell Carcinoma

(<b>Purpose</b>) Previous studies have pointed out the significance of IgG Fc binding protein (FCGBP) in carcinogenesis, cancer progression, and tumor immunity in certain malignancies. However, its prognostic values, molecular interaction, and immune characteristics in the head and neck...

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Main Authors: Yu-Hsuan Lin, Yi-Fang Yang, Yow-Ling Shiue
Format: Article
Language:English
Published: MDPI AG 2022-05-01
Series:Diagnostics
Subjects:
Online Access:https://www.mdpi.com/2075-4418/12/5/1178
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author Yu-Hsuan Lin
Yi-Fang Yang
Yow-Ling Shiue
author_facet Yu-Hsuan Lin
Yi-Fang Yang
Yow-Ling Shiue
author_sort Yu-Hsuan Lin
collection DOAJ
description (<b>Purpose</b>) Previous studies have pointed out the significance of IgG Fc binding protein (FCGBP) in carcinogenesis, cancer progression, and tumor immunity in certain malignancies. However, its prognostic values, molecular interaction, and immune characteristics in the head and neck squamous cell carcinoma (HNSC) remained unclear. (<b>Methods</b>) To evaluate the potential role of the <i>FCGBP</i> gene, we used GEPIA2 and UALCAN platforms to explore the differential levels, survivals, and genetic alteration through cBioPortal (based on The Cancer Genome Atlas dataset). STRING, GeneMania, and TIMER2.0 identified the interacting networks. LinkedOmics performed Gene enrichment analysis, and TISIDB and TIMER2.0 evaluated the role of <i>FCGBP</i> in the tumor microenvironment. (<b>Results</b>) The expression level of <i>FCGBP</i> is lower in cancer tissues. A high <i>FCGBP</i> level is significantly associated with better overall- and disease-specific-survivals, regardless of human papillomavirus infection. Low <i>FCGBP</i> levels correlated to a higher <i>tumor protein p53</i> (<i>TP53)</i> mutation rate (<i>p</i> = 0.018). <i>FCGBP</i> alteration significantly co-occurred with that of <i>TP53</i> (<i>q =</i> 0.037). Interacting networks revealed a significant association between FGFBP and trefoil factor 3 (TFF3), a novel prognostic marker in various cancers, at transcriptional and translational levels. Enrichment analyses identified that the top gene sets predominantly related to immune and inflammatory responses. Further investigation found that the <i>FCGBP</i> mRNA level positively correlated to the infiltration rates of B cells, Th17/CD8+ T lymphocytes, T helper follicular cells, mast cells, and expression levels of various immune molecules and immune checkpoints in HNSC. (<b>Conclusions</b>) We found that the <i>FCGBP</i> mRNA level negatively correlated to <i>TP53</i> mutation status while positively correlated to the <i>TFF3</i> level. Additionally, FCGBP may regulate the tumor microenvironment. These findings support the <i>FCGBP</i> as a potential biomarker to estimate HNSC prognoses.
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spelling doaj.art-b692ecab77c2427da1da3690c15a75bc2023-11-23T10:40:30ZengMDPI AGDiagnostics2075-44182022-05-01125117810.3390/diagnostics12051178Multi-Omics Analyses to Identify FCGBP as a Potential Predictor in Head and Neck Squamous Cell CarcinomaYu-Hsuan Lin0Yi-Fang Yang1Yow-Ling Shiue2Institute of Biomedical Sciences, National Sun Yat-sen University, Kaohsiung 804, TaiwanDepartment of Medical Education and Research, Kaohsiung Veterans General Hospital, Kaohsiung 813, TaiwanInstitute of Biomedical Sciences, National Sun Yat-sen University, Kaohsiung 804, Taiwan(<b>Purpose</b>) Previous studies have pointed out the significance of IgG Fc binding protein (FCGBP) in carcinogenesis, cancer progression, and tumor immunity in certain malignancies. However, its prognostic values, molecular interaction, and immune characteristics in the head and neck squamous cell carcinoma (HNSC) remained unclear. (<b>Methods</b>) To evaluate the potential role of the <i>FCGBP</i> gene, we used GEPIA2 and UALCAN platforms to explore the differential levels, survivals, and genetic alteration through cBioPortal (based on The Cancer Genome Atlas dataset). STRING, GeneMania, and TIMER2.0 identified the interacting networks. LinkedOmics performed Gene enrichment analysis, and TISIDB and TIMER2.0 evaluated the role of <i>FCGBP</i> in the tumor microenvironment. (<b>Results</b>) The expression level of <i>FCGBP</i> is lower in cancer tissues. A high <i>FCGBP</i> level is significantly associated with better overall- and disease-specific-survivals, regardless of human papillomavirus infection. Low <i>FCGBP</i> levels correlated to a higher <i>tumor protein p53</i> (<i>TP53)</i> mutation rate (<i>p</i> = 0.018). <i>FCGBP</i> alteration significantly co-occurred with that of <i>TP53</i> (<i>q =</i> 0.037). Interacting networks revealed a significant association between FGFBP and trefoil factor 3 (TFF3), a novel prognostic marker in various cancers, at transcriptional and translational levels. Enrichment analyses identified that the top gene sets predominantly related to immune and inflammatory responses. Further investigation found that the <i>FCGBP</i> mRNA level positively correlated to the infiltration rates of B cells, Th17/CD8+ T lymphocytes, T helper follicular cells, mast cells, and expression levels of various immune molecules and immune checkpoints in HNSC. (<b>Conclusions</b>) We found that the <i>FCGBP</i> mRNA level negatively correlated to <i>TP53</i> mutation status while positively correlated to the <i>TFF3</i> level. Additionally, FCGBP may regulate the tumor microenvironment. These findings support the <i>FCGBP</i> as a potential biomarker to estimate HNSC prognoses.https://www.mdpi.com/2075-4418/12/5/1178head neck squamous cell carcinomaIgG Fc binding proteinFCGBPprognosistumor microenvironmentimmune
spellingShingle Yu-Hsuan Lin
Yi-Fang Yang
Yow-Ling Shiue
Multi-Omics Analyses to Identify FCGBP as a Potential Predictor in Head and Neck Squamous Cell Carcinoma
Diagnostics
head neck squamous cell carcinoma
IgG Fc binding protein
FCGBP
prognosis
tumor microenvironment
immune
title Multi-Omics Analyses to Identify FCGBP as a Potential Predictor in Head and Neck Squamous Cell Carcinoma
title_full Multi-Omics Analyses to Identify FCGBP as a Potential Predictor in Head and Neck Squamous Cell Carcinoma
title_fullStr Multi-Omics Analyses to Identify FCGBP as a Potential Predictor in Head and Neck Squamous Cell Carcinoma
title_full_unstemmed Multi-Omics Analyses to Identify FCGBP as a Potential Predictor in Head and Neck Squamous Cell Carcinoma
title_short Multi-Omics Analyses to Identify FCGBP as a Potential Predictor in Head and Neck Squamous Cell Carcinoma
title_sort multi omics analyses to identify fcgbp as a potential predictor in head and neck squamous cell carcinoma
topic head neck squamous cell carcinoma
IgG Fc binding protein
FCGBP
prognosis
tumor microenvironment
immune
url https://www.mdpi.com/2075-4418/12/5/1178
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AT yifangyang multiomicsanalysestoidentifyfcgbpasapotentialpredictorinheadandnecksquamouscellcarcinoma
AT yowlingshiue multiomicsanalysestoidentifyfcgbpasapotentialpredictorinheadandnecksquamouscellcarcinoma