Systemic Profiling of KDM5 Subfamily Signature in Non-Small-Cell Lung Cancer

Fang Hao Department of Oncology, Tianjin Medical University General Hospital, Tianjin, People’s Republic of ChinaCorrespondence: Fang Hao Email haofang@tmu.edu.cnBackground: Despite improvements in diagnosis and treatment, lung cancer is one of the most lethal human diseases, with a dismal 5-year re...

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Main Author: Hao F
Format: Article
Language:English
Published: Dove Medical Press 2021-10-01
Series:International Journal of General Medicine
Subjects:
Online Access:https://www.dovepress.com/systemic-profiling-of-kdm5-subfamily-signature-in-non-small-cell-lung--peer-reviewed-fulltext-article-IJGM
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author Hao F
author_facet Hao F
author_sort Hao F
collection DOAJ
description Fang Hao Department of Oncology, Tianjin Medical University General Hospital, Tianjin, People’s Republic of ChinaCorrespondence: Fang Hao Email haofang@tmu.edu.cnBackground: Despite improvements in diagnosis and treatment, lung cancer is one of the most lethal human diseases, with a dismal 5-year relative survival rate of only 5% for patients diagnosed with advanced metastatic disease. Accumulating evidence supports that epigenetic aberration of histone demethylase-KDM5 subfamily is linked to human pan-cancer. However, the detailed functions of KDM5 proteins in lung cancer, especially in non-small-cell lung cancer (NSCLC), remain poorly understand.Methods: UALCAN, GEPIA, Kaplan–Meier plotter, cBioPortal, TIMER, TISIDB, and STRING databases were utilized in this investigation.Results: We detected varying degrees of gene mutations of KDM5 subfamily members and found that KDM5B/C were remarkably overexpressed in LUAD and LUSC compared to normal tissues. Different from KDM5D, positive relationship was shown between overall survival and mRNA expression of KDM5A/B/C in lung cancer. We determined that KDM5A/B/C expression levels were positively correlated with CD4+ T cells infiltration, especially immunological markers of Tregs and Th17 cells. Moreover, LUAD and LUSC were separately rich in inflammatory and wound healing subtypes after immunogenomics analyzing with respect to KDM5 subfamily overexpression. And with their 120 co-expressed genes, we revealed that nucleocytoplasmic transport and cellular protein localization-related genes were closely connected to KDM5 subfamily alterations, next to chromatin remodeling genes.Conclusion: We formulated the immune-infiltrating and prognostic value of KDM5 subfamily and highlighted its promising role in immune-inflammatory interaction with tumour microenvironment in NSCLC.Keywords: non-small-cell lung cancer, biomarker, KDM5 subfamily, bioinformatics analysis, immune cell infiltration
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spelling doaj.art-e7f03d8fe8fe456d9e4621f8f09216d82022-12-21T20:09:31ZengDove Medical PressInternational Journal of General Medicine1178-70742021-10-01Volume 147259727570053Systemic Profiling of KDM5 Subfamily Signature in Non-Small-Cell Lung CancerHao FFang Hao Department of Oncology, Tianjin Medical University General Hospital, Tianjin, People’s Republic of ChinaCorrespondence: Fang Hao Email haofang@tmu.edu.cnBackground: Despite improvements in diagnosis and treatment, lung cancer is one of the most lethal human diseases, with a dismal 5-year relative survival rate of only 5% for patients diagnosed with advanced metastatic disease. Accumulating evidence supports that epigenetic aberration of histone demethylase-KDM5 subfamily is linked to human pan-cancer. However, the detailed functions of KDM5 proteins in lung cancer, especially in non-small-cell lung cancer (NSCLC), remain poorly understand.Methods: UALCAN, GEPIA, Kaplan–Meier plotter, cBioPortal, TIMER, TISIDB, and STRING databases were utilized in this investigation.Results: We detected varying degrees of gene mutations of KDM5 subfamily members and found that KDM5B/C were remarkably overexpressed in LUAD and LUSC compared to normal tissues. Different from KDM5D, positive relationship was shown between overall survival and mRNA expression of KDM5A/B/C in lung cancer. We determined that KDM5A/B/C expression levels were positively correlated with CD4+ T cells infiltration, especially immunological markers of Tregs and Th17 cells. Moreover, LUAD and LUSC were separately rich in inflammatory and wound healing subtypes after immunogenomics analyzing with respect to KDM5 subfamily overexpression. And with their 120 co-expressed genes, we revealed that nucleocytoplasmic transport and cellular protein localization-related genes were closely connected to KDM5 subfamily alterations, next to chromatin remodeling genes.Conclusion: We formulated the immune-infiltrating and prognostic value of KDM5 subfamily and highlighted its promising role in immune-inflammatory interaction with tumour microenvironment in NSCLC.Keywords: non-small-cell lung cancer, biomarker, KDM5 subfamily, bioinformatics analysis, immune cell infiltrationhttps://www.dovepress.com/systemic-profiling-of-kdm5-subfamily-signature-in-non-small-cell-lung--peer-reviewed-fulltext-article-IJGMnon-small-cell lung cancerbiomarkerkdm5 subfamilybioinformatics analysisimmune cell infiltration
spellingShingle Hao F
Systemic Profiling of KDM5 Subfamily Signature in Non-Small-Cell Lung Cancer
International Journal of General Medicine
non-small-cell lung cancer
biomarker
kdm5 subfamily
bioinformatics analysis
immune cell infiltration
title Systemic Profiling of KDM5 Subfamily Signature in Non-Small-Cell Lung Cancer
title_full Systemic Profiling of KDM5 Subfamily Signature in Non-Small-Cell Lung Cancer
title_fullStr Systemic Profiling of KDM5 Subfamily Signature in Non-Small-Cell Lung Cancer
title_full_unstemmed Systemic Profiling of KDM5 Subfamily Signature in Non-Small-Cell Lung Cancer
title_short Systemic Profiling of KDM5 Subfamily Signature in Non-Small-Cell Lung Cancer
title_sort systemic profiling of kdm5 subfamily signature in non small cell lung cancer
topic non-small-cell lung cancer
biomarker
kdm5 subfamily
bioinformatics analysis
immune cell infiltration
url https://www.dovepress.com/systemic-profiling-of-kdm5-subfamily-signature-in-non-small-cell-lung--peer-reviewed-fulltext-article-IJGM
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