» Articles » PMID: 37239411

LncRNA TRHDE-AS1 Correlated with Genomic Landscape and Clinical Outcome in Glioma

Overview
Journal Genes (Basel)
Publisher MDPI
Date 2023 May 27
PMID 37239411
Authors
Affiliations
Soon will be listed here.
Abstract

The role of lncRNA in cancer development has received more and more attention in research. A variety of lncRNAs are associated with the occurrence and development of glioma. However, the role of TRHDE-AS1 in glioma is still unknown. In this study, we explored the role of TRHDE-AS1 in glioma through bioinformatic methods. We first identified an association between TRHDE-AS1 and tumor prognosis in pan-cancer analysis. Subsequently, the expression levels of TRHDE-AS1 in various clinical types of glioma were compared, and significant differences were found in pathological classification, WHO classification, molecular classification, IDH mutation, and age stratification. We analyzed the genes co-expressed with TRHDE-AS1 in glioma. In the functional analysis of TRHDE-AS1, we found that TRHDE-AS1 may be involved in the regulation of synapse-related functions. In glioma cancer driver gene correlation analysis, it was also found that TRHDE-AS1 was significantly correlated with the expression levels of multiple driver genes such as TP53, BRAF, and IDH1. By comparing the mutant profiles of the high and low TRHDE-AS1 groups, we also found that there may be differences in TP53 and CIC gene mutations in low-grade gliomas. Subsequent correlation analysis between TRHDE-AS1 and glioma immune microenvironment showed that the expression level of TRHDE-AS1 was correlated with a variety of immune cells. Therefore, we believe that TRHDE-AS1 is involved in the occurrence and development of glioma and has the ability to predict the prognosis of glioma as a biomarker of glioma.

Citing Articles

expression is associated with lung adenocarcinoma prognosis and immune infiltration and regulates lung adenocarcinoma cell proliferation and metastasis through the MAPK/ERK pathway.

Xu S, Xu Y, Chai W, Liu X, Li J, Sun L J Thorac Dis. 2024; 16(6):3764-3781.

PMID: 38983163 PMC: 11228747. DOI: 10.21037/jtd-24-8.


The pathogenesis mechanism and potential clinical value of lncRNA in gliomas.

Liu Y, Yuan H, Fan J, Wang H, Xie H, Wan J Discov Oncol. 2024; 15(1):266.

PMID: 38967893 PMC: 11226588. DOI: 10.1007/s12672-024-01144-4.

References
1.
Malkin D, Li F, Strong L, Fraumeni Jr J, Nelson C, Kim D . Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms. Science. 1990; 250(4985):1233-8. DOI: 10.1126/science.1978757. View

2.
Panni S, Lovering R, Porras P, Orchard S . Non-coding RNA regulatory networks. Biochim Biophys Acta Gene Regul Mech. 2019; 1863(6):194417. DOI: 10.1016/j.bbagrm.2019.194417. View

3.
Fan Y, Potdar A, Gong Y, Eswarappa S, Donnola S, Lathia J . Profilin-1 phosphorylation directs angiocrine expression and glioblastoma progression through HIF-1α accumulation. Nat Cell Biol. 2014; 16(5):445-56. PMC: 4036069. DOI: 10.1038/ncb2954. View

4.
Wolf D, Harris N, Rotter V . Reconstitution of p53 expression in a nonproducer Ab-MuLV-transformed cell line by transfection of a functional p53 gene. Cell. 1984; 38(1):119-26. DOI: 10.1016/0092-8674(84)90532-4. View

5.
Lu Z, Chen Y, Chen S, Zhu X, Wang C, Wang Z . Comprehensive Prognostic Analysis of Immune Implication Value and Oxidative Stress Significance of NECAP2 in Low-Grade Glioma. Oxid Med Cell Longev. 2022; 2022:1494520. PMC: 9750773. DOI: 10.1155/2022/1494520. View