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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...

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Autores principales: Shen, Yiming, Wei, Zhengyu, Zhou, Chongchang, Song, Jiangping, Wang, Jianing, Wang, Jiada, Wu, Linrong, Fang, Shenzhe, Shen, Zhisen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
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.
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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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