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pmid:39154317

A comprehensive analysis of TRP-related gene signature, and immune infiltration in patients with colorectal cancer.

Yicheng Liu · Xiaobing Yao · Wenjun Zhao · Jin Xu · Haiyan Zhang · Ting Huang · Chuang Wu · Jiajia Yang · Cheng Tang · Qianqian Ye · Weiye Hu · Qingming Wang

Discover oncology · 2024 doi:10.1007/s12672-024-01227-2

Paper

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Experiment

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Data

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A comprehensive analysis of TRP-related gene signature, and immune infiltration in patients with colorectal cancer.
doi
10.1007/s12672-024-01227-2
pmid
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Yicheng Liu
[1]
Xiaobing Yao
[2]
Wenjun Zhao
[3]
Jin Xu
[4]
Haiyan Zhang
[5]
Ting Huang
[6]
Chuang Wu
[7]
Jiajia Yang
[8]
Cheng Tang
[9]
Qianqian Ye
[10]
Weiye Hu
[11]
Qingming Wang
journal
Discover oncology
year
2024
abstract
BACKGROUND: Transient receptor potential (TRP) channels are involved in the development and progression of tumors. However, their role in colorectal cancer (CRC) remains unclear, and this study aims to investigate the role of TRP-related genes in CRC. METHODS: Data was obtained from The Cancer Genome Atlas (TCGA) database, and analyses were conducted on the GSE14333 and GSE38832 datasets to assess the prognosis and mark TRP-related genes (TRGs). Subsequently, clustering analysis and immune infiltration analysis were performed to explore the relevant TRGs. In vitro validation of key TRGs' gene and protein expression was conducted using human colon cancer cells. RESULTS: Compared to normal tissues, 8 TRGs were significantly upregulated in CRC, while 11 were downregulated. TRPA1 was identified as a protective prognostic factor, whereas TRPM5 (HR = 1.349), TRPV4 (HR = 1.289), and TRPV3 (HR = 1.442) were identified as prognostic risk factors. Receiver operating characteristic (ROC) curves and Kaplan-Meier (KM) analyses yielded similar results. Additionally, lower expression of TRPA1 and higher expression of TRPV4 and TRPM5 were negatively correlated with patient prognosis, and experimental validation confirmed the underexpression of TRPA1 and overexpression of TRPV4 and TRPM5 in CRC cell lines. CONCLUSION: This study identifies a TRP channel-related prognosis in CRC, providing a novel approach to stratifying CRC prognosis.
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RNA-sequencing data and clinical data were downloaded from The Cancer Genome Atlas (TCGA, https://cancergenome.nih.gov/) and The Genotype-Tissue Expression (GTEx, https://gtexportal.org/home/datasets) database. All data supporting the findings of this study were available from the corresponding author upon reasonable request.
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However, their role in colorectal cancer (CRC) remains unclear, and this study aims to investigate the role of TRP-related genes in CRC.\nMETHODS: Data was obtained from The Cancer Genome Atlas (TCGA) database, and analyses were conducted on the GSE14333 and GSE38832 datasets to assess the prognosis and mark TRP-related genes (TRGs). Subsequently, clustering analysis and immune infiltration analysis were performed to explore the relevant TRGs. In vitro validation of key TRGs' gene and protein expression was conducted using human colon cancer cells.\nRESULTS: Compared to normal tissues, 8 TRGs were significantly upregulated in CRC, while 11 were downregulated. TRPA1 was identified as a protective prognostic factor, whereas TRPM5 (HR = 1.349), TRPV4 (HR = 1.289), and TRPV3 (HR = 1.442) were identified as prognostic risk factors. Receiver operating characteristic (ROC) curves and Kaplan-Meier (KM) analyses yielded similar results. 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