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Effect of PFKFB4 on the Prognosis and Immune Regulation of NSCLC and Its Mechanism

BACKGROUND: NSCLC (non-small cell lung cancer) has become the malignancy with the highest incidence and mortality rate worldwide. Fructose-6-phosphate 2-kinase/fructose-2,6-bisphosphatase 4 (PFKFB4) is a key regulator of glycolysis with both kinase and phosphatase activities. The Warburg effect, or...

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Autores principales: Zhou, Yong, Fan, Yongfei, Qiu, Binzhe, Lou, Ming, Liu, Xiaoshuang, Yuan, Kai, Tong, Jichun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9356739/
https://www.ncbi.nlm.nih.gov/pubmed/35942289
http://dx.doi.org/10.2147/IJGM.S369126
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author Zhou, Yong
Fan, Yongfei
Qiu, Binzhe
Lou, Ming
Liu, Xiaoshuang
Yuan, Kai
Tong, Jichun
author_facet Zhou, Yong
Fan, Yongfei
Qiu, Binzhe
Lou, Ming
Liu, Xiaoshuang
Yuan, Kai
Tong, Jichun
author_sort Zhou, Yong
collection PubMed
description BACKGROUND: NSCLC (non-small cell lung cancer) has become the malignancy with the highest incidence and mortality rate worldwide. Fructose-6-phosphate 2-kinase/fructose-2,6-bisphosphatase 4 (PFKFB4) is a key regulator of glycolysis with both kinase and phosphatase activities. The Warburg effect, or increased glycolysis in tumors, provides the metabolic basis for cancer cell proliferation and metastasis, and the Warburg pathway enzyme PFKFB4 is a newly identified important kinase. This study aimed to elucidate the poor prognostic relevance of PFKFB4 in non-small cell lung cancer tissues and its relationship with immune cell infiltration, immune cell biomarkers, and immune checkpoints. METHODS: In this study, immunohistochemical methods were used to assess PFKFB4 expression levels in 140 surgical specimens from patients with histologically confirmed non-small cell lung cancer and to investigate the relationship between PFKFB4 expression levels and the patients’ clinicopathological characteristics. The impact of PFKFB4 expression on prognosis was evaluated using Kaplan–Meier survival analysis and Cox regression analysis. RESULTS: When compared to normal paracrine tissues, PFKFB4 expression was enhanced in lung cancer tissues, and Kaplan–Meier survival analysis revealed that patients with high PFKFB4 expression had a worse prognosis. In NSCLC, PFKFB4 was found to be associated with immune cell infiltration and immunological checkpoints. CONCLUSION: PFKFB4 expression may be upregulated as a sign of poor prognosis in NSCLC, and PFKFB4 may be implicated not only in the genesis and progression of NSCLC but also in its immunological control.
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spelling pubmed-93567392022-08-07 Effect of PFKFB4 on the Prognosis and Immune Regulation of NSCLC and Its Mechanism Zhou, Yong Fan, Yongfei Qiu, Binzhe Lou, Ming Liu, Xiaoshuang Yuan, Kai Tong, Jichun Int J Gen Med Original Research BACKGROUND: NSCLC (non-small cell lung cancer) has become the malignancy with the highest incidence and mortality rate worldwide. Fructose-6-phosphate 2-kinase/fructose-2,6-bisphosphatase 4 (PFKFB4) is a key regulator of glycolysis with both kinase and phosphatase activities. The Warburg effect, or increased glycolysis in tumors, provides the metabolic basis for cancer cell proliferation and metastasis, and the Warburg pathway enzyme PFKFB4 is a newly identified important kinase. This study aimed to elucidate the poor prognostic relevance of PFKFB4 in non-small cell lung cancer tissues and its relationship with immune cell infiltration, immune cell biomarkers, and immune checkpoints. METHODS: In this study, immunohistochemical methods were used to assess PFKFB4 expression levels in 140 surgical specimens from patients with histologically confirmed non-small cell lung cancer and to investigate the relationship between PFKFB4 expression levels and the patients’ clinicopathological characteristics. The impact of PFKFB4 expression on prognosis was evaluated using Kaplan–Meier survival analysis and Cox regression analysis. RESULTS: When compared to normal paracrine tissues, PFKFB4 expression was enhanced in lung cancer tissues, and Kaplan–Meier survival analysis revealed that patients with high PFKFB4 expression had a worse prognosis. In NSCLC, PFKFB4 was found to be associated with immune cell infiltration and immunological checkpoints. CONCLUSION: PFKFB4 expression may be upregulated as a sign of poor prognosis in NSCLC, and PFKFB4 may be implicated not only in the genesis and progression of NSCLC but also in its immunological control. Dove 2022-08-02 /pmc/articles/PMC9356739/ /pubmed/35942289 http://dx.doi.org/10.2147/IJGM.S369126 Text en © 2022 Zhou et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Zhou, Yong
Fan, Yongfei
Qiu, Binzhe
Lou, Ming
Liu, Xiaoshuang
Yuan, Kai
Tong, Jichun
Effect of PFKFB4 on the Prognosis and Immune Regulation of NSCLC and Its Mechanism
title Effect of PFKFB4 on the Prognosis and Immune Regulation of NSCLC and Its Mechanism
title_full Effect of PFKFB4 on the Prognosis and Immune Regulation of NSCLC and Its Mechanism
title_fullStr Effect of PFKFB4 on the Prognosis and Immune Regulation of NSCLC and Its Mechanism
title_full_unstemmed Effect of PFKFB4 on the Prognosis and Immune Regulation of NSCLC and Its Mechanism
title_short Effect of PFKFB4 on the Prognosis and Immune Regulation of NSCLC and Its Mechanism
title_sort effect of pfkfb4 on the prognosis and immune regulation of nsclc and its mechanism
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9356739/
https://www.ncbi.nlm.nih.gov/pubmed/35942289
http://dx.doi.org/10.2147/IJGM.S369126
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