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Kynureninase Promotes Immunosuppression and Predicts Survival in Glioma Patients: In Silico Data Analyses of the Chinese Glioma Genome Atlas (CGGA) and of the Cancer Genome Atlas (TCGA)

Kynureninase (KYNU) is a kynurenine pathway (KP) enzyme that produces metabolites with immunomodulatory properties. In recent years, overactivation of KP has been associated with poor prognosis of several types of cancer, in particular by promoting the invasion, metastasis, and chemoresistance of ca...

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Autores principales: Pérez de la Cruz, Gonzalo, Pérez de la Cruz, Verónica, Navarro Cossio, Javier, Vázquez Cervantes, Gustavo Ignacio, Salazar, Aleli, Orozco Morales, Mario, Pineda, Benjamin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10051585/
https://www.ncbi.nlm.nih.gov/pubmed/36986469
http://dx.doi.org/10.3390/ph16030369
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author Pérez de la Cruz, Gonzalo
Pérez de la Cruz, Verónica
Navarro Cossio, Javier
Vázquez Cervantes, Gustavo Ignacio
Salazar, Aleli
Orozco Morales, Mario
Pineda, Benjamin
author_facet Pérez de la Cruz, Gonzalo
Pérez de la Cruz, Verónica
Navarro Cossio, Javier
Vázquez Cervantes, Gustavo Ignacio
Salazar, Aleli
Orozco Morales, Mario
Pineda, Benjamin
author_sort Pérez de la Cruz, Gonzalo
collection PubMed
description Kynureninase (KYNU) is a kynurenine pathway (KP) enzyme that produces metabolites with immunomodulatory properties. In recent years, overactivation of KP has been associated with poor prognosis of several types of cancer, in particular by promoting the invasion, metastasis, and chemoresistance of cancer cells. However, the role of KYNU in gliomas remains to be explored. In this study, we used the available data from TCGA, CGGA and GTEx projects to analyze KYNU expression in gliomas and healthy tissue, as well as the potential contribution of KYNU in the tumor immune infiltrate. In addition, immune-related genes were screened with KYNU expression. KYNU expression correlated with the increased malignancy of astrocytic tumors. Survival analysis in primary astrocytomas showed that KYNU expression correlated with poor prognosis. Additionally, KYNU expression correlated positively with several genes related to an immunosuppressive microenvironment and with the characteristic immune tumor infiltrate. These findings indicate that KYNU could be a potential therapeutic target for modulating the tumor microenvironment and enhancing an effective antitumor immune response.
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spelling pubmed-100515852023-03-30 Kynureninase Promotes Immunosuppression and Predicts Survival in Glioma Patients: In Silico Data Analyses of the Chinese Glioma Genome Atlas (CGGA) and of the Cancer Genome Atlas (TCGA) Pérez de la Cruz, Gonzalo Pérez de la Cruz, Verónica Navarro Cossio, Javier Vázquez Cervantes, Gustavo Ignacio Salazar, Aleli Orozco Morales, Mario Pineda, Benjamin Pharmaceuticals (Basel) Article Kynureninase (KYNU) is a kynurenine pathway (KP) enzyme that produces metabolites with immunomodulatory properties. In recent years, overactivation of KP has been associated with poor prognosis of several types of cancer, in particular by promoting the invasion, metastasis, and chemoresistance of cancer cells. However, the role of KYNU in gliomas remains to be explored. In this study, we used the available data from TCGA, CGGA and GTEx projects to analyze KYNU expression in gliomas and healthy tissue, as well as the potential contribution of KYNU in the tumor immune infiltrate. In addition, immune-related genes were screened with KYNU expression. KYNU expression correlated with the increased malignancy of astrocytic tumors. Survival analysis in primary astrocytomas showed that KYNU expression correlated with poor prognosis. Additionally, KYNU expression correlated positively with several genes related to an immunosuppressive microenvironment and with the characteristic immune tumor infiltrate. These findings indicate that KYNU could be a potential therapeutic target for modulating the tumor microenvironment and enhancing an effective antitumor immune response. MDPI 2023-02-28 /pmc/articles/PMC10051585/ /pubmed/36986469 http://dx.doi.org/10.3390/ph16030369 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Pérez de la Cruz, Gonzalo
Pérez de la Cruz, Verónica
Navarro Cossio, Javier
Vázquez Cervantes, Gustavo Ignacio
Salazar, Aleli
Orozco Morales, Mario
Pineda, Benjamin
Kynureninase Promotes Immunosuppression and Predicts Survival in Glioma Patients: In Silico Data Analyses of the Chinese Glioma Genome Atlas (CGGA) and of the Cancer Genome Atlas (TCGA)
title Kynureninase Promotes Immunosuppression and Predicts Survival in Glioma Patients: In Silico Data Analyses of the Chinese Glioma Genome Atlas (CGGA) and of the Cancer Genome Atlas (TCGA)
title_full Kynureninase Promotes Immunosuppression and Predicts Survival in Glioma Patients: In Silico Data Analyses of the Chinese Glioma Genome Atlas (CGGA) and of the Cancer Genome Atlas (TCGA)
title_fullStr Kynureninase Promotes Immunosuppression and Predicts Survival in Glioma Patients: In Silico Data Analyses of the Chinese Glioma Genome Atlas (CGGA) and of the Cancer Genome Atlas (TCGA)
title_full_unstemmed Kynureninase Promotes Immunosuppression and Predicts Survival in Glioma Patients: In Silico Data Analyses of the Chinese Glioma Genome Atlas (CGGA) and of the Cancer Genome Atlas (TCGA)
title_short Kynureninase Promotes Immunosuppression and Predicts Survival in Glioma Patients: In Silico Data Analyses of the Chinese Glioma Genome Atlas (CGGA) and of the Cancer Genome Atlas (TCGA)
title_sort kynureninase promotes immunosuppression and predicts survival in glioma patients: in silico data analyses of the chinese glioma genome atlas (cgga) and of the cancer genome atlas (tcga)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10051585/
https://www.ncbi.nlm.nih.gov/pubmed/36986469
http://dx.doi.org/10.3390/ph16030369
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