A novel inflammation-related lncRNAs prognostic signature identifies LINC00346 in promoting proliferation, migration, and immune infiltration of glioma

In this study, a total of 13 inflammation-related lncRNAs with a high prognostic value were identified with univariate, multivariate Cox regression analysis, and LASSO analysis. LINC00346, which is one of the 13 lncRNAs identified, was positively associated with type 2 macrophage activation and the...

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Main Authors: Wen-Jing Zeng, Lei Zhang, Hui Cao, Dongjie Li, Hao Zhang, Zhiwei Xia, Renjun Peng
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-10-01
Series:Frontiers in Immunology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fimmu.2022.810572/full
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author Wen-Jing Zeng
Lei Zhang
Hui Cao
Dongjie Li
Hao Zhang
Zhiwei Xia
Renjun Peng
Renjun Peng
author_facet Wen-Jing Zeng
Lei Zhang
Hui Cao
Dongjie Li
Hao Zhang
Zhiwei Xia
Renjun Peng
Renjun Peng
author_sort Wen-Jing Zeng
collection DOAJ
description In this study, a total of 13 inflammation-related lncRNAs with a high prognostic value were identified with univariate, multivariate Cox regression analysis, and LASSO analysis. LINC00346, which is one of the 13 lncRNAs identified, was positively associated with type 2 macrophage activation and the malignant degree of glioma. Fluorescence in situ hybridization (FISH) and immunohistochemical staining showed that LINC00346 was highly expressed in high-grade glioma, while type 2 macrophages key transcription factor STAT3 and surface marker CD204 were also highly expressed simultaneously. LINC00346 high-expression gliomas were more sensitive to the anti–PD-1 and anti-CTLA-4 therapy. LINC00346 was also associated with tumor proliferation and tumor migration validated by EdU, cell colony, formation CCK8, and transwell assays. These findings reveal novel biomarkers for predicting glioma prognosis and outline relationships between lncRNAs inflammation, and glioma, as well as possible immune checkpoint targets for glioma.
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spelling doaj.art-15466ae974414dc19aff873bc15a95ca2022-12-22T04:30:22ZengFrontiers Media S.A.Frontiers in Immunology1664-32242022-10-011310.3389/fimmu.2022.810572810572A novel inflammation-related lncRNAs prognostic signature identifies LINC00346 in promoting proliferation, migration, and immune infiltration of gliomaWen-Jing Zeng0Lei Zhang1Hui Cao2Dongjie Li3Hao Zhang4Zhiwei Xia5Renjun Peng6Renjun Peng7Department of Pharmarcy, Xiangya Hospital, Central South University, Changsha, ChinaDepartment of Neurology, Beijing Hospital, National Center of Gerontology, Institute of Geriatric Medicine, Chinese Academy of Medical Science, Beijing, ChinaDepartment of Psychiatry, The Second People’s Hospital of Hunan Province, The Hospital of Hunan University of Chinese Medicine, Changsha, ChinaDepartment of Geriatrics, Xiangya International Medical Center, Xiangya Hospital, Central South University, Changsha, ChinaDepartment of Neurosurgery, Xiangya Hospital, Central South University, Changsha, ChinaDepartment of Neurology, Hunan Aerospace Hospital, Changsha Medical University, Changsha, ChinaDepartment of Neurosurgery, Xiangya Hospital, Central South University, Changsha, ChinaNational Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Changsha, ChinaIn this study, a total of 13 inflammation-related lncRNAs with a high prognostic value were identified with univariate, multivariate Cox regression analysis, and LASSO analysis. LINC00346, which is one of the 13 lncRNAs identified, was positively associated with type 2 macrophage activation and the malignant degree of glioma. Fluorescence in situ hybridization (FISH) and immunohistochemical staining showed that LINC00346 was highly expressed in high-grade glioma, while type 2 macrophages key transcription factor STAT3 and surface marker CD204 were also highly expressed simultaneously. LINC00346 high-expression gliomas were more sensitive to the anti–PD-1 and anti-CTLA-4 therapy. LINC00346 was also associated with tumor proliferation and tumor migration validated by EdU, cell colony, formation CCK8, and transwell assays. These findings reveal novel biomarkers for predicting glioma prognosis and outline relationships between lncRNAs inflammation, and glioma, as well as possible immune checkpoint targets for glioma.https://www.frontiersin.org/articles/10.3389/fimmu.2022.810572/fullgliomalncRNAinflammationprognostictarget
spellingShingle Wen-Jing Zeng
Lei Zhang
Hui Cao
Dongjie Li
Hao Zhang
Zhiwei Xia
Renjun Peng
Renjun Peng
A novel inflammation-related lncRNAs prognostic signature identifies LINC00346 in promoting proliferation, migration, and immune infiltration of glioma
Frontiers in Immunology
glioma
lncRNA
inflammation
prognostic
target
title A novel inflammation-related lncRNAs prognostic signature identifies LINC00346 in promoting proliferation, migration, and immune infiltration of glioma
title_full A novel inflammation-related lncRNAs prognostic signature identifies LINC00346 in promoting proliferation, migration, and immune infiltration of glioma
title_fullStr A novel inflammation-related lncRNAs prognostic signature identifies LINC00346 in promoting proliferation, migration, and immune infiltration of glioma
title_full_unstemmed A novel inflammation-related lncRNAs prognostic signature identifies LINC00346 in promoting proliferation, migration, and immune infiltration of glioma
title_short A novel inflammation-related lncRNAs prognostic signature identifies LINC00346 in promoting proliferation, migration, and immune infiltration of glioma
title_sort novel inflammation related lncrnas prognostic signature identifies linc00346 in promoting proliferation migration and immune infiltration of glioma
topic glioma
lncRNA
inflammation
prognostic
target
url https://www.frontiersin.org/articles/10.3389/fimmu.2022.810572/full
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