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NLRC3 is a potential prognostic biomarker that is correlated with immune cell infiltration in lung adenocarcinoma

The NLR family CARD domain containing 3 (NLRC3) gene has been reported to have a crucial effect on immunity, inflammation, and tumorigenesis. However, the clinical relevance of NLRC3 in lung adenocarcinoma (LUAD) remains unclear. This study analyzed both RNA sequencing data and corresponding clinica...

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Autores principales: Zhuo, Yingchen, Li, Xueqian, Feng, Weiyi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9941471/
https://www.ncbi.nlm.nih.gov/pubmed/36808166
http://dx.doi.org/10.1038/s41598-022-23979-z
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author Zhuo, Yingchen
Li, Xueqian
Feng, Weiyi
author_facet Zhuo, Yingchen
Li, Xueqian
Feng, Weiyi
author_sort Zhuo, Yingchen
collection PubMed
description The NLR family CARD domain containing 3 (NLRC3) gene has been reported to have a crucial effect on immunity, inflammation, and tumorigenesis. However, the clinical relevance of NLRC3 in lung adenocarcinoma (LUAD) remains unclear. This study analyzed both RNA sequencing data and corresponding clinical outcomes obtained from public databases to identify (i) NLRC3 as a tumor suppressor in LUAD and (ii) its predictive value for the likelihood of patient responsiveness to immunotherapy. The results showed that NLRC3 expression was reduced in LUAD and was lower in advanced-stage tumors. Additionally, reduced NLRC3 expression was correlated with worse patient prognosis. The protein level of NLRC3 was also observed to have prognostic significance. Moreover, downregulation of NLRC3 was found to suppress the chemotaxis and infiltration of antitumor lymphocyte subpopulations as well as natural killer cells. Mechanistic analysis indicated that NLRC3 may be involved in immune infiltration by regulating chemokines and their receptors in LUAD. Furthermore, NLRC3 functions as a molecular switch in macrophages, whereby it mediates the polarization of M1 macrophages. Patients with high NLRC3 expression were also found to exhibit a more promising response to immunotherapy. In conclusion, NLRC3 could serve as a potential prognostic biomarker for LUAD, help predict the immunotherapeutic response of patients, and guide personalized strategies for the treatment of LUAD.
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spelling pubmed-99414712023-02-22 NLRC3 is a potential prognostic biomarker that is correlated with immune cell infiltration in lung adenocarcinoma Zhuo, Yingchen Li, Xueqian Feng, Weiyi Sci Rep Article The NLR family CARD domain containing 3 (NLRC3) gene has been reported to have a crucial effect on immunity, inflammation, and tumorigenesis. However, the clinical relevance of NLRC3 in lung adenocarcinoma (LUAD) remains unclear. This study analyzed both RNA sequencing data and corresponding clinical outcomes obtained from public databases to identify (i) NLRC3 as a tumor suppressor in LUAD and (ii) its predictive value for the likelihood of patient responsiveness to immunotherapy. The results showed that NLRC3 expression was reduced in LUAD and was lower in advanced-stage tumors. Additionally, reduced NLRC3 expression was correlated with worse patient prognosis. The protein level of NLRC3 was also observed to have prognostic significance. Moreover, downregulation of NLRC3 was found to suppress the chemotaxis and infiltration of antitumor lymphocyte subpopulations as well as natural killer cells. Mechanistic analysis indicated that NLRC3 may be involved in immune infiltration by regulating chemokines and their receptors in LUAD. Furthermore, NLRC3 functions as a molecular switch in macrophages, whereby it mediates the polarization of M1 macrophages. Patients with high NLRC3 expression were also found to exhibit a more promising response to immunotherapy. In conclusion, NLRC3 could serve as a potential prognostic biomarker for LUAD, help predict the immunotherapeutic response of patients, and guide personalized strategies for the treatment of LUAD. Nature Publishing Group UK 2023-02-20 /pmc/articles/PMC9941471/ /pubmed/36808166 http://dx.doi.org/10.1038/s41598-022-23979-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Zhuo, Yingchen
Li, Xueqian
Feng, Weiyi
NLRC3 is a potential prognostic biomarker that is correlated with immune cell infiltration in lung adenocarcinoma
title NLRC3 is a potential prognostic biomarker that is correlated with immune cell infiltration in lung adenocarcinoma
title_full NLRC3 is a potential prognostic biomarker that is correlated with immune cell infiltration in lung adenocarcinoma
title_fullStr NLRC3 is a potential prognostic biomarker that is correlated with immune cell infiltration in lung adenocarcinoma
title_full_unstemmed NLRC3 is a potential prognostic biomarker that is correlated with immune cell infiltration in lung adenocarcinoma
title_short NLRC3 is a potential prognostic biomarker that is correlated with immune cell infiltration in lung adenocarcinoma
title_sort nlrc3 is a potential prognostic biomarker that is correlated with immune cell infiltration in lung adenocarcinoma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9941471/
https://www.ncbi.nlm.nih.gov/pubmed/36808166
http://dx.doi.org/10.1038/s41598-022-23979-z
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