TY - JOUR
T1 - Mining TCGA database for prognostic genes in head and neck squamous cell carcinoma microenvironment
AU - Ran, Qiu Chi
AU - Long, Sheng Rong
AU - Ye, Yan
AU - Xie, Chen
AU - XuXiao, Zhuo Lin
AU - Liu, Yu Song
AU - Pang, Hong Xia
AU - Sunchuri, Diwas
AU - Teng, Nai Chia
AU - Guo, Zhu Ling
N1 - Funding Information:
All the authors thank Dr. Guangyu Li for supporting this paper. This research was funded by Scientific Research Fund of Hainan Provincial Education Department ( Hnky2020ZD-19 ), Young Talents’ Science and Technology Innovation Project of Hainan Association for Science and Technology ( QCXM201817 ), Educational scientific Research of Hainan Medical University ( HYYB202014 ), Marxism Theory Discipline Research Project of Hainan Medical University ( QMYKYLX201807 ), Research Project of Hainan Provincial Humanities Medical Research Base ( QRYZH201811(YB) ).
Publisher Copyright:
© 2020 Association for Dental Sciences of the Republic of China
Copyright:
Copyright 2020 Elsevier B.V., All rights reserved.
PY - 2021/3
Y1 - 2021/3
N2 - Background/purpose: Head and neck squamous cell carcinoma (HNSCC) is one of the most common malignant tumors. The aim of this study was to elucidate the effect of tumor microenvironment-related genes on the prognosis of HNSCC and to obtain tumor microenvironment-related genes that can predict poor prognosis in HNSCC patients. Materials and methods: The ESTIMATE algorithm was applied to the HNSCC transcriptomic data downloaded from the TCGA (The cancer genome atlas), and then the samples were divided into two groups: high and low immune scoring groups, and high and low basal scoring groups to screen for differentially expressed genes (DEGs) associated with poor patient outcomes. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis was performed to explore the potential functions of DEGs, and then to explore the potential prognostic value of individual DEGs. The results of survival analysis between DEGs and overall survival (OS) to explore tumor microenvironment-related genes relevant to the prognosis of HNSCC patients. Results: Fifty-nine tumor microenvironment-related genes were screened for association of OS with HNSCC (P < 0.05). The GO and KEGG enrichment analysis showed that the selected DEGs may mediate immune response, extracellular matrix, and immunoglobulin binding via neutrophil activation in HNSCC. Six of these DEGs, GIMAP6, SELL, TIFAB, KCNA3, P2RY8 and CCR4 were most significantly associated with OS (P < 0.001). Conclusion: We identified six tumor microenvironment-related genes that were significantly associated with poor prognosis in HNSCC. These genes may inspire researchers to discover new targets and approaches for HNSCC treatment.
AB - Background/purpose: Head and neck squamous cell carcinoma (HNSCC) is one of the most common malignant tumors. The aim of this study was to elucidate the effect of tumor microenvironment-related genes on the prognosis of HNSCC and to obtain tumor microenvironment-related genes that can predict poor prognosis in HNSCC patients. Materials and methods: The ESTIMATE algorithm was applied to the HNSCC transcriptomic data downloaded from the TCGA (The cancer genome atlas), and then the samples were divided into two groups: high and low immune scoring groups, and high and low basal scoring groups to screen for differentially expressed genes (DEGs) associated with poor patient outcomes. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis was performed to explore the potential functions of DEGs, and then to explore the potential prognostic value of individual DEGs. The results of survival analysis between DEGs and overall survival (OS) to explore tumor microenvironment-related genes relevant to the prognosis of HNSCC patients. Results: Fifty-nine tumor microenvironment-related genes were screened for association of OS with HNSCC (P < 0.05). The GO and KEGG enrichment analysis showed that the selected DEGs may mediate immune response, extracellular matrix, and immunoglobulin binding via neutrophil activation in HNSCC. Six of these DEGs, GIMAP6, SELL, TIFAB, KCNA3, P2RY8 and CCR4 were most significantly associated with OS (P < 0.001). Conclusion: We identified six tumor microenvironment-related genes that were significantly associated with poor prognosis in HNSCC. These genes may inspire researchers to discover new targets and approaches for HNSCC treatment.
KW - HNSCC
KW - Immune scores
KW - TCGA
KW - Tumor microenvironment
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U2 - 10.1016/j.jds.2020.09.017
DO - 10.1016/j.jds.2020.09.017
M3 - Article
AN - SCOPUS:85092651647
SN - 1991-7902
VL - 16
SP - 661
EP - 667
JO - Journal of Dental Sciences
JF - Journal of Dental Sciences
IS - 2
ER -