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NALCN is a potential biomarker and therapeutic target in human cancers

Background: Sodium leak channel non-selective (NALCN), known as a voltage-independent Na(+) channel, is increasingly considered to play vital roles in tumorigenesis and metastasis of human cancers. However, no comprehensive pan-cancer analysis of NALCN has been conducted. Our study aims to explore t...

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Autores principales: He, Jian, Xu, Jie, Chang, Zhiwei, Yan, Jiaqin, Zhang, Limin, Qin, Yanru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10154523/
https://www.ncbi.nlm.nih.gov/pubmed/37152978
http://dx.doi.org/10.3389/fgene.2023.1164707
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author He, Jian
Xu, Jie
Chang, Zhiwei
Yan, Jiaqin
Zhang, Limin
Qin, Yanru
author_facet He, Jian
Xu, Jie
Chang, Zhiwei
Yan, Jiaqin
Zhang, Limin
Qin, Yanru
author_sort He, Jian
collection PubMed
description Background: Sodium leak channel non-selective (NALCN), known as a voltage-independent Na(+) channel, is increasingly considered to play vital roles in tumorigenesis and metastasis of human cancers. However, no comprehensive pan-cancer analysis of NALCN has been conducted. Our study aims to explore the potential diagnostic, prognostic and therapeutic value of NALCN in human cancers. Methods: Through comprehensive application of datasets from Human Protein Atlas (HPA), The Cancer Genome Atlas (TCGA), Cancer Cell Line Encyclopedia (CCLE), Enhanced Version of Tumor Immune Estimation Resource (TIMER2.0), Tumor and Immune System Interaction Database (TISIDB), The University of Alabama at Birmingham Cancer data analysis Portal (UALCAN), cBioPortal, GeneMANIA and Search Tool for the Retrieval of Interaction Gene/Proteins (STRING) databases, we explored the potential roles of NALCN in different cancers. The differential expression, prognostic implications, pathological stages and grades, molecular and immune subtypes, diagnostic accuracy, tumor mutation burden (TMB), microsatellite instability (MSI), mismatch repair (MMR) genes, immune checkpoint genes, chemokine genes, major histocompatibility complex (MHC)-related genes, tumor-infiltrating immune cells (TIICs), promoter methylation, mutations, copy number alteration (CNA), and functional enrichment related to NALCN were analyzed. Results: Most cancers lowly expressed NALCN. Upregulated NALCN expression was associated with poor or better prognosis in different cancers. Moreover, NALCN was correlated with clinicopathological features in multiple cancers. NALCN showed high diagnostic accuracy in 5 caner types. NALCN is highly linked with immune-related biomarkers, immune-related genes and TIICs. Significant methylation changes and genetic alteration of NALCN can be observed in many cancers. Enrichment analysis showed that NALCN is closely related to multiple tumor-related signaling pathways. Conclusion: Our study revealed the vital involvement of NALCN in cancer. NALCN can be used as a prognostic biomarker for immune infiltration and clinical outcomes, and has potential diagnostic and therapeutic implications.
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spelling pubmed-101545232023-05-04 NALCN is a potential biomarker and therapeutic target in human cancers He, Jian Xu, Jie Chang, Zhiwei Yan, Jiaqin Zhang, Limin Qin, Yanru Front Genet Genetics Background: Sodium leak channel non-selective (NALCN), known as a voltage-independent Na(+) channel, is increasingly considered to play vital roles in tumorigenesis and metastasis of human cancers. However, no comprehensive pan-cancer analysis of NALCN has been conducted. Our study aims to explore the potential diagnostic, prognostic and therapeutic value of NALCN in human cancers. Methods: Through comprehensive application of datasets from Human Protein Atlas (HPA), The Cancer Genome Atlas (TCGA), Cancer Cell Line Encyclopedia (CCLE), Enhanced Version of Tumor Immune Estimation Resource (TIMER2.0), Tumor and Immune System Interaction Database (TISIDB), The University of Alabama at Birmingham Cancer data analysis Portal (UALCAN), cBioPortal, GeneMANIA and Search Tool for the Retrieval of Interaction Gene/Proteins (STRING) databases, we explored the potential roles of NALCN in different cancers. The differential expression, prognostic implications, pathological stages and grades, molecular and immune subtypes, diagnostic accuracy, tumor mutation burden (TMB), microsatellite instability (MSI), mismatch repair (MMR) genes, immune checkpoint genes, chemokine genes, major histocompatibility complex (MHC)-related genes, tumor-infiltrating immune cells (TIICs), promoter methylation, mutations, copy number alteration (CNA), and functional enrichment related to NALCN were analyzed. Results: Most cancers lowly expressed NALCN. Upregulated NALCN expression was associated with poor or better prognosis in different cancers. Moreover, NALCN was correlated with clinicopathological features in multiple cancers. NALCN showed high diagnostic accuracy in 5 caner types. NALCN is highly linked with immune-related biomarkers, immune-related genes and TIICs. Significant methylation changes and genetic alteration of NALCN can be observed in many cancers. Enrichment analysis showed that NALCN is closely related to multiple tumor-related signaling pathways. Conclusion: Our study revealed the vital involvement of NALCN in cancer. NALCN can be used as a prognostic biomarker for immune infiltration and clinical outcomes, and has potential diagnostic and therapeutic implications. Frontiers Media S.A. 2023-04-19 /pmc/articles/PMC10154523/ /pubmed/37152978 http://dx.doi.org/10.3389/fgene.2023.1164707 Text en Copyright © 2023 He, Xu, Chang, Yan, Zhang and Qin. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
He, Jian
Xu, Jie
Chang, Zhiwei
Yan, Jiaqin
Zhang, Limin
Qin, Yanru
NALCN is a potential biomarker and therapeutic target in human cancers
title NALCN is a potential biomarker and therapeutic target in human cancers
title_full NALCN is a potential biomarker and therapeutic target in human cancers
title_fullStr NALCN is a potential biomarker and therapeutic target in human cancers
title_full_unstemmed NALCN is a potential biomarker and therapeutic target in human cancers
title_short NALCN is a potential biomarker and therapeutic target in human cancers
title_sort nalcn is a potential biomarker and therapeutic target in human cancers
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10154523/
https://www.ncbi.nlm.nih.gov/pubmed/37152978
http://dx.doi.org/10.3389/fgene.2023.1164707
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