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pmid:39678513

A comprehensive investigation of PRMT5 in the prognosis and ion channel features of lung cancer.

Yan Wang · Daifang Chu · Haichao Li · Jiangjiang Fan · Ximing Zhu · Yulong Ma · Zhongping Gu · Nianlin Xie · Pengyu Jing

Frontiers in oncology · 2024 doi:10.3389/fonc.2024.1478672

Paper

complete

Experiment

complete

Data

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Analysis

partial

Execution

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title
A comprehensive investigation of PRMT5 in the prognosis and ion channel features of lung cancer.
doi
10.3389/fonc.2024.1478672
pmid
39678513
authors array · 9 items
[0]
Yan Wang
[1]
Daifang Chu
[2]
Haichao Li
[3]
Jiangjiang Fan
[4]
Ximing Zhu
[5]
Yulong Ma
[6]
Zhongping Gu
[7]
Nianlin Xie
[8]
Pengyu Jing
journal
Frontiers in oncology
year
2024
abstract
The increasing incidence and mortality associated with lung cancer (LC) is a significant global health challenge. The underlying mechanisms contributing to LC remain inadequately understood. However, emerging evidence suggests that the epigenetic modifier protein arginine methyltransferase 5 (PRMT5) plays a complex role in various cellular processes, including DNA repair, gene transcription, and alternative splicing, through its function in catalyzing the symmetric dimethylation of both histone and non-histone proteins. In this study, we examined the functional role of PRMT5 utilizing LC-related datasets (GSE30219, GSE50081, and TCGA LC cohort) through a series of analyses. Our findings revealed that PRMT5 was significantly overexpressed in LC samples compared to normal tissues and was correlated with overall survival and disease-free survival rates. Additionally, PRDM1 was identified as a key protein exhibiting a strong interaction with PRMT5. The prognostic model that integrated PRMT5 with clinical factors demonstrated robust performance in assessing survival outcomes. Elevated levels of PRMT5 were associated with poor prognosis in LC, as evidenced by analyses of the GSE30219, GSE50081, and TCGA-LC datasets. Furthermore, we identified 27 ion channel (IC) genes exhibited a correlation with PRMT5 in lung adenocarcinoma (LUAD), of which 9 genes were identified as statistically significant with KM survival analysis. Strikingly, all of the 9 genes, including LRRC8A, the same as PRMT5, were associated with poor prognosis in LUAD. Our research highlights the potential of PRMT5 as a novel prognostic biomarker and its relationship with IC genes in LC.
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Subsequently, based on the database of UCSC XEAN (https://xena.ucsc.edu/), the pearson correlation was analyzed between IC-related genes and PRMT5 in TCGA-LUAD gene expression data.
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Subsequently, based on the database of UCSC XEAN (https://xena.ucsc.edu/), the pearson correlation was analyzed between IC-related genes and PRMT5 in TCGA-LUAD gene expression data.
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The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/ Supplementary Material .
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Elevated levels of PRMT5 were associated with poor prognosis in LC, as evidenced by analyses of the GSE30219, GSE50081, and TCGA-LC datasets.
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Elevated levels of PRMT5 were associated with poor prognosis in LC, as evidenced by analyses of the GSE30219, GSE50081, and TCGA-LC datasets.
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title
Validation of a histology-independent prognostic gene signature for early stage, non-small cell lung cancer including stage IA patients
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Subsequently, based on the database of UCSC XEAN (https://xena.ucsc.edu/), the pearson correlation was analyzed between IC-related genes and PRMT5 in TCGA-LUAD gene expression data.
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Subsequently, based on the database of UCSC XEAN (https://xena.ucsc.edu/), the pearson correlation was analyzed between IC-related genes and PRMT5 in TCGA-LUAD gene expression data.
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However, emerging evidence suggests that the epigenetic modifier protein arginine methyltransferase 5 (PRMT5) plays a complex role in various cellular processes, including DNA repair, gene transcription, and alternative splicing, through its function in catalyzing the symmetric dimethylation of both histone and non-histone proteins. In this study, we examined the functional role of PRMT5 utilizing LC-related datasets (GSE30219, GSE50081, and TCGA LC cohort) through a series of analyses. Our findings revealed that PRMT5 was significantly overexpressed in LC samples compared to normal tissues and was correlated with overall survival and disease-free survival rates. Additionally, PRDM1 was identified as a key protein exhibiting a strong interaction with PRMT5. The prognostic model that integrated PRMT5 with clinical factors demonstrated robust performance in assessing survival outcomes. Elevated levels of PRMT5 were associated with poor prognosis in LC, as evidenced by analyses of the GSE30219, GSE50081, and TCGA-LC datasets. Furthermore, we identified 27 ion channel (IC) genes exhibited a correlation with PRMT5 in lung adenocarcinoma (LUAD), of which 9 genes were identified as statistically significant with KM survival analysis. Strikingly, all of the 9 genes, including LRRC8A, the same as PRMT5, were associated with poor prognosis in LUAD. 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