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Arylsulfatase I is a prognostic biomarker for head and neck squamous cell carcinoma and Pan‐cancer
BACKGROUND: Sulfatase gene family members mediate various biological functions in tumor stroma and tumor cell environments. However, the expressions and prognostic value of Arylsulfatase I (ARSI), a sulfatase gene family member, in head and neck squamous cell carcinoma (HNSC) have not been fully est...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9459304/ https://www.ncbi.nlm.nih.gov/pubmed/35870182 http://dx.doi.org/10.1002/jcla.24600 |
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author | Shen, Yiming Wei, Zhengyu Zhou, Chongchang Song, Jiangping Wang, Jianing Wang, Jiada Wu, Linrong Fang, Shenzhe Shen, Zhisen |
author_facet | Shen, Yiming Wei, Zhengyu Zhou, Chongchang Song, Jiangping Wang, Jianing Wang, Jiada Wu, Linrong Fang, Shenzhe Shen, Zhisen |
author_sort | Shen, Yiming |
collection | PubMed |
description | BACKGROUND: Sulfatase gene family members mediate various biological functions in tumor stroma and tumor cell environments. However, the expressions and prognostic value of Arylsulfatase I (ARSI), a sulfatase gene family member, in head and neck squamous cell carcinoma (HNSC) have not been fully established. METHODS: Arylsulfatase I expressions in pan‐cancer were profiled using publicly available databases. Then, univariate Cox regression, Kaplan–Meier, and the Pearson's correlation analyses were performed to determine correlations between ARSI expressions and cancer prognosis, immune cell status, and drug sensitivity. Gene set variation analysis (GSVA) and gene set enrichment analysis (GSEA) were used to assess the potential mechanisms underlying ARSI functions in HNSC. RESULTS: Arylsulfatase I was highly expressed in 15 cancer types, with significant expressions in HNSC. Elevated ARSI levels were associated with worse prognostic outcomes in HNSC patients. In addition, GSVA and GSEA showed that ARSI was highly involved in tumor cell escape and inflammatory responses. Expressions of ARSI negatively correlated with tumor mutation burden or microsatellite instability and positively correlated with immune‐related genes. Elevated ARSI expressions conferred poor tolerance to daporinad and sinularin, but increased cell sensitivity to dasatinib and XAV939. CONCLUSION: Arylsulfatase I is a promising prognostic and therapeutic target for HNSC. |
format | Online Article Text |
id | pubmed-9459304 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-94593042022-09-12 Arylsulfatase I is a prognostic biomarker for head and neck squamous cell carcinoma and Pan‐cancer Shen, Yiming Wei, Zhengyu Zhou, Chongchang Song, Jiangping Wang, Jianing Wang, Jiada Wu, Linrong Fang, Shenzhe Shen, Zhisen J Clin Lab Anal Research Articles BACKGROUND: Sulfatase gene family members mediate various biological functions in tumor stroma and tumor cell environments. However, the expressions and prognostic value of Arylsulfatase I (ARSI), a sulfatase gene family member, in head and neck squamous cell carcinoma (HNSC) have not been fully established. METHODS: Arylsulfatase I expressions in pan‐cancer were profiled using publicly available databases. Then, univariate Cox regression, Kaplan–Meier, and the Pearson's correlation analyses were performed to determine correlations between ARSI expressions and cancer prognosis, immune cell status, and drug sensitivity. Gene set variation analysis (GSVA) and gene set enrichment analysis (GSEA) were used to assess the potential mechanisms underlying ARSI functions in HNSC. RESULTS: Arylsulfatase I was highly expressed in 15 cancer types, with significant expressions in HNSC. Elevated ARSI levels were associated with worse prognostic outcomes in HNSC patients. In addition, GSVA and GSEA showed that ARSI was highly involved in tumor cell escape and inflammatory responses. Expressions of ARSI negatively correlated with tumor mutation burden or microsatellite instability and positively correlated with immune‐related genes. Elevated ARSI expressions conferred poor tolerance to daporinad and sinularin, but increased cell sensitivity to dasatinib and XAV939. CONCLUSION: Arylsulfatase I is a promising prognostic and therapeutic target for HNSC. John Wiley and Sons Inc. 2022-07-23 /pmc/articles/PMC9459304/ /pubmed/35870182 http://dx.doi.org/10.1002/jcla.24600 Text en © 2022 The Authors. Journal of Clinical Laboratory Analysis published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Shen, Yiming Wei, Zhengyu Zhou, Chongchang Song, Jiangping Wang, Jianing Wang, Jiada Wu, Linrong Fang, Shenzhe Shen, Zhisen Arylsulfatase I is a prognostic biomarker for head and neck squamous cell carcinoma and Pan‐cancer |
title |
Arylsulfatase I is a prognostic biomarker for head and neck squamous cell carcinoma and Pan‐cancer |
title_full |
Arylsulfatase I is a prognostic biomarker for head and neck squamous cell carcinoma and Pan‐cancer |
title_fullStr |
Arylsulfatase I is a prognostic biomarker for head and neck squamous cell carcinoma and Pan‐cancer |
title_full_unstemmed |
Arylsulfatase I is a prognostic biomarker for head and neck squamous cell carcinoma and Pan‐cancer |
title_short |
Arylsulfatase I is a prognostic biomarker for head and neck squamous cell carcinoma and Pan‐cancer |
title_sort | arylsulfatase i is a prognostic biomarker for head and neck squamous cell carcinoma and pan‐cancer |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9459304/ https://www.ncbi.nlm.nih.gov/pubmed/35870182 http://dx.doi.org/10.1002/jcla.24600 |
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