Back to Search Start Over

TRP Family Genes Are Differently Expressed and Correlated with Immune Response in Glioma.

Authors :
Fang, Chaoyou
Xu, Houshi
Liu, Yibo
Huang, Chenkai
Wang, Xiaoyu
Zhang, Zeyu
Xu, Yuanzhi
Yuan, Ling
Zhang, Anke
Shao, Anwen
Lou, Meiqing
Source :
Brain Sciences (2076-3425). May2022, Vol. 12 Issue 5, p662. 15p.
Publication Year :
2022

Abstract

(1) Background: glioma is the most prevalent primary tumor of the human central nervous system and accompanies extremely poor prognosis in patients. The transient receptor potential (TRP) channels family consists of six different families, which are closely associated with cancer cell proliferation, differentiation, migration, and invasion. TRP family genes play an essential role in the development of tumors. Nevertheless, the function of these genes in gliomas is not fully understood. (2) Methods: we analyze the gene expression data of 28 TRP family genes in glioma patients through bioinformatic analysis. (3) Results: the study showed the aberrations of TRP family genes were correlated to prognosis in glioma. Then, we set enrichment analysis and selected 10 hub genes that may play an important role in glioma. Meanwhile, the expression of 10 hub genes was further established according to different grades, survival time, IDH mutation status, and 1p/19q codeletion status. We found that TRPC1, TRPC3, TRPC4, TRPC5, TRPC6, MCOLN1, MCOLN2, and MCOLN3 were significantly correlated to the prognosis in glioma patients. Furthermore, we illustrated that the expression of hub genes was associated with immune activation and immunoregulators (immunoinhibitors, immunostimulators, and MHC molecules) in glioma. (4) Conclusions: we proved that TRP family genes are promising immunotherapeutic targets and potential clinical biomarkers in patients with glioma. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20763425
Volume :
12
Issue :
5
Database :
Academic Search Index
Journal :
Brain Sciences (2076-3425)
Publication Type :
Academic Journal
Accession number :
157128651
Full Text :
https://doi.org/10.3390/brainsci12050662