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Expression and Prognostic Value of Glucose Transporter 3 in Diffuse Large B Cell Lymphoma

BACKGROUND: Several reports have suggested that glucose transporter 3 (GLUT-3) promotes tumor metastasis. The aim of this study was to examine the relationship between the expression level of GLUT-3 and the prognosis of patients with diffuse large B cell lymphoma (DLBCL). METHODS: The GLUT-3 express...

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Autores principales: Xu, Yongpeng, Zhou, Xinglu, Zhang, Shuai, Nanding, Abiyasi, Xuan, Qijia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8888198/
https://www.ncbi.nlm.nih.gov/pubmed/35250277
http://dx.doi.org/10.2147/OTT.S338826
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author Xu, Yongpeng
Zhou, Xinglu
Zhang, Shuai
Nanding, Abiyasi
Xuan, Qijia
author_facet Xu, Yongpeng
Zhou, Xinglu
Zhang, Shuai
Nanding, Abiyasi
Xuan, Qijia
author_sort Xu, Yongpeng
collection PubMed
description BACKGROUND: Several reports have suggested that glucose transporter 3 (GLUT-3) promotes tumor metastasis. The aim of this study was to examine the relationship between the expression level of GLUT-3 and the prognosis of patients with diffuse large B cell lymphoma (DLBCL). METHODS: The GLUT-3 expression levels in 91 DLBCL patients were evaluated by immunohistochemistry. The relationships between GLUT-3 expression level and clinicopathological characteristics and progression-free survival (PFS) of DLBCL patients were analyzed. The use of validation cohorts confirmed the predictive value of GLUT-3 expression. The correlation between GLUT-3 and immune cell infiltration was investigated using the Cell-type Identification By Estimating Relative Subsets Of RNA Transcripts system and the analysis of the infiltrating score was obtained by single sample Gene Set Enrichment Analysis. RESULTS: Expression of GLUT-3, which is highly expressed in DLBCL patients, was significantly associated with elevated serum LDH level, recurrence and Ki-67 status. Kaplan–Meier analysis showed that high GLUT-3 expression levels in DLBCL were related to poor PFS. Univariate and multivariate analyses results showed that low GLUT-3 expression level was significantly but independently associated with favorable PFS in DLBCL patients. GLUT-3 expression was also correlated with immune cell infiltration and the analysis of the infiltrating score. CONCLUSION: Our results indicate that GLUT-3 may act as a potential independent prognostic factor in DLBCL patients. The difference of the immune microenvironment in DLBCL patients may be predicted by the expression level of GLUT-3.
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spelling pubmed-88881982022-03-03 Expression and Prognostic Value of Glucose Transporter 3 in Diffuse Large B Cell Lymphoma Xu, Yongpeng Zhou, Xinglu Zhang, Shuai Nanding, Abiyasi Xuan, Qijia Onco Targets Ther Original Research BACKGROUND: Several reports have suggested that glucose transporter 3 (GLUT-3) promotes tumor metastasis. The aim of this study was to examine the relationship between the expression level of GLUT-3 and the prognosis of patients with diffuse large B cell lymphoma (DLBCL). METHODS: The GLUT-3 expression levels in 91 DLBCL patients were evaluated by immunohistochemistry. The relationships between GLUT-3 expression level and clinicopathological characteristics and progression-free survival (PFS) of DLBCL patients were analyzed. The use of validation cohorts confirmed the predictive value of GLUT-3 expression. The correlation between GLUT-3 and immune cell infiltration was investigated using the Cell-type Identification By Estimating Relative Subsets Of RNA Transcripts system and the analysis of the infiltrating score was obtained by single sample Gene Set Enrichment Analysis. RESULTS: Expression of GLUT-3, which is highly expressed in DLBCL patients, was significantly associated with elevated serum LDH level, recurrence and Ki-67 status. Kaplan–Meier analysis showed that high GLUT-3 expression levels in DLBCL were related to poor PFS. Univariate and multivariate analyses results showed that low GLUT-3 expression level was significantly but independently associated with favorable PFS in DLBCL patients. GLUT-3 expression was also correlated with immune cell infiltration and the analysis of the infiltrating score. CONCLUSION: Our results indicate that GLUT-3 may act as a potential independent prognostic factor in DLBCL patients. The difference of the immune microenvironment in DLBCL patients may be predicted by the expression level of GLUT-3. Dove 2022-02-25 /pmc/articles/PMC8888198/ /pubmed/35250277 http://dx.doi.org/10.2147/OTT.S338826 Text en © 2022 Xu 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
Xu, Yongpeng
Zhou, Xinglu
Zhang, Shuai
Nanding, Abiyasi
Xuan, Qijia
Expression and Prognostic Value of Glucose Transporter 3 in Diffuse Large B Cell Lymphoma
title Expression and Prognostic Value of Glucose Transporter 3 in Diffuse Large B Cell Lymphoma
title_full Expression and Prognostic Value of Glucose Transporter 3 in Diffuse Large B Cell Lymphoma
title_fullStr Expression and Prognostic Value of Glucose Transporter 3 in Diffuse Large B Cell Lymphoma
title_full_unstemmed Expression and Prognostic Value of Glucose Transporter 3 in Diffuse Large B Cell Lymphoma
title_short Expression and Prognostic Value of Glucose Transporter 3 in Diffuse Large B Cell Lymphoma
title_sort expression and prognostic value of glucose transporter 3 in diffuse large b cell lymphoma
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8888198/
https://www.ncbi.nlm.nih.gov/pubmed/35250277
http://dx.doi.org/10.2147/OTT.S338826
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