The Potential Impact of HNRNPA2B1 on Human Cancers Prognosis and Immune Microenvironment

HNRNPA2B1 is a member of the HNRNP family, which is associated with telomere function, mRNA translation, and splicing, and plays an important role in tumor development. To date, there have been no pan-cancer studies of HNRNPA2B1, particularly within the TME. Therefore, we conducted a pan-cancer anal...

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Main Authors: Tao Huang, Gang Zhu, Fan Chen
Format: Article
Language:English
Published: Wiley 2024-01-01
Series:Journal of Immunology Research
Online Access:http://dx.doi.org/10.1155/2024/5515307
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author Tao Huang
Gang Zhu
Fan Chen
author_facet Tao Huang
Gang Zhu
Fan Chen
author_sort Tao Huang
collection DOAJ
description HNRNPA2B1 is a member of the HNRNP family, which is associated with telomere function, mRNA translation, and splicing, and plays an important role in tumor development. To date, there have been no pan-cancer studies of HNRNPA2B1, particularly within the TME. Therefore, we conducted a pan-cancer analysis of HNRNPA2B1 using TCGA data. Based on datasets from TCGA, TARGET, Genotype-Tissue Expression, and Human Protein Atlas, we employed a range of bioinformatics approaches to explore the potential oncogenic role of HNRNPA2B1. This included analyzing the association of HNRNPA2B1 expression with prognosis, tumor mutation burden (TMB), microsatellite instability (MSI), immune response, and immune cell infiltration of individual tumors. We further validated the bioinformatic findings using immunohistochemistry techniques. HNRNPA2B1 was found to be differentially expressed across most tumor types in TCGA’s pan-cancer database and was predictive of poorer clinical staging and survival status. HNRNPA2B1 expression was also closely linked to TMB, MSI, tumor stemness, and chemotherapy response. HNRNPA2B1 plays a significant role in the TME and is involved in the regulation of novel immunotherapies. Its expression is significantly associated with the infiltration of macrophages, dendritic cells, NK cells, and T cells. Furthermore, HNRNPA2B1 is closely associated with immune checkpoints, immune-stimulatory genes, immune-inhibitory genes, MHC genes, chemokines, and chemokine receptors. We performed a comprehensive evaluation of HNRNPA2B1, revealing its potential role as a prognostic indicator for patients and its immunomodulatory functions.
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spelling doaj-art-55b0946a917642438a2166ce376f00a72025-02-03T10:46:38ZengWileyJournal of Immunology Research2314-71562024-01-01202410.1155/2024/5515307The Potential Impact of HNRNPA2B1 on Human Cancers Prognosis and Immune MicroenvironmentTao Huang0Gang Zhu1Fan Chen2Department of NeurosurgeryDepartment of NeurosurgeryDepartment of NeurosurgeryHNRNPA2B1 is a member of the HNRNP family, which is associated with telomere function, mRNA translation, and splicing, and plays an important role in tumor development. To date, there have been no pan-cancer studies of HNRNPA2B1, particularly within the TME. Therefore, we conducted a pan-cancer analysis of HNRNPA2B1 using TCGA data. Based on datasets from TCGA, TARGET, Genotype-Tissue Expression, and Human Protein Atlas, we employed a range of bioinformatics approaches to explore the potential oncogenic role of HNRNPA2B1. This included analyzing the association of HNRNPA2B1 expression with prognosis, tumor mutation burden (TMB), microsatellite instability (MSI), immune response, and immune cell infiltration of individual tumors. We further validated the bioinformatic findings using immunohistochemistry techniques. HNRNPA2B1 was found to be differentially expressed across most tumor types in TCGA’s pan-cancer database and was predictive of poorer clinical staging and survival status. HNRNPA2B1 expression was also closely linked to TMB, MSI, tumor stemness, and chemotherapy response. HNRNPA2B1 plays a significant role in the TME and is involved in the regulation of novel immunotherapies. Its expression is significantly associated with the infiltration of macrophages, dendritic cells, NK cells, and T cells. Furthermore, HNRNPA2B1 is closely associated with immune checkpoints, immune-stimulatory genes, immune-inhibitory genes, MHC genes, chemokines, and chemokine receptors. We performed a comprehensive evaluation of HNRNPA2B1, revealing its potential role as a prognostic indicator for patients and its immunomodulatory functions.http://dx.doi.org/10.1155/2024/5515307
spellingShingle Tao Huang
Gang Zhu
Fan Chen
The Potential Impact of HNRNPA2B1 on Human Cancers Prognosis and Immune Microenvironment
Journal of Immunology Research
title The Potential Impact of HNRNPA2B1 on Human Cancers Prognosis and Immune Microenvironment
title_full The Potential Impact of HNRNPA2B1 on Human Cancers Prognosis and Immune Microenvironment
title_fullStr The Potential Impact of HNRNPA2B1 on Human Cancers Prognosis and Immune Microenvironment
title_full_unstemmed The Potential Impact of HNRNPA2B1 on Human Cancers Prognosis and Immune Microenvironment
title_short The Potential Impact of HNRNPA2B1 on Human Cancers Prognosis and Immune Microenvironment
title_sort potential impact of hnrnpa2b1 on human cancers prognosis and immune microenvironment
url http://dx.doi.org/10.1155/2024/5515307
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