» Articles » PMID: 34873574

Hub Gene and Its Key Effects on Diffuse Large B-Cell Lymphoma by Weighted Gene Coexpression Network Analysis

Overview
Journal Biomed Res Int
Publisher Wiley
Date 2021 Dec 7
PMID 34873574
Citations 3
Authors
Affiliations
Soon will be listed here.
Abstract

Diffuse large B-cell lymphoma (DLBC) is a kind of tumor with rapid progress and poor prognosis. Therefore, it is necessary to explore new biomarkers or therapeutic targets to assist in diagnosis or treatment. This study is aimed at screening hub genes by weighted gene coexpression network analysis (WGCNA) and exploring the significance of overall survival (OS) in DLBC patients. Statistical data using WGCNA to analyze mRNA expression in DLBC patients came from The Cancer Genome Atlas (TCGA) dataset. After analyzing with clinical information, the biological functions of hub genes were detected. Survival analysis, Cox regression detection, and correlation analysis of the hub genes were carried out. The potential function of the hub gene related to prognosis was predicted by gene set enrichment analysis (GSEA). The results showed that , , , and expression in normal tissues was significantly higher than that in cancer tissues ( < 0.01). Survival analysis showed that patients with high and were associated with better OS ( < 0.01). and genes were mainly enriched in the regulation of ROS and oxidative stress. The two hub genes related to the prognosis of DLBC were identified and verified based on WGCNA. Survival analysis showed that the overexpression of and in DLBC might be beneficial to the prognosis. These findings identified vital pathways and genes that may become new therapeutic targets and contribute to prognostic indicators.

Citing Articles

Identification of immune-related genes and development of a prognostic model in mantle cell lymphoma.

Zhang W, Shi J, Wang H, Zhang T, Zhou X, Zhang H Ann Transl Med. 2023; 10(24):1323.

PMID: 36660618 PMC: 9843426. DOI: 10.21037/atm-22-5815.


Integrative Bioinformatics Analysis Reveals CHEK1 and UBE2C as Luminal A Breast Cancer Subtype Biomarkers.

Yu D, Liu S, Chen Y, Yang L Front Genet. 2022; 13:944259.

PMID: 35903365 PMC: 9322798. DOI: 10.3389/fgene.2022.944259.


A Potential Diagnostic and Prognostic Biomarker TMEM176B and Its Relationship With Immune Infiltration in Skin Cutaneous Melanoma.

Jiang L, Yang Y, Liu F, Ma M, Gao J, Sun L Front Cell Dev Biol. 2022; 10:859958.

PMID: 35399535 PMC: 8986129. DOI: 10.3389/fcell.2022.859958.

References
1.
ROCHEFORT H . Cathepsin D in breast cancer: a tissue marker associated with metastasis. Eur J Cancer. 1992; 28A(11):1780-3. DOI: 10.1016/0959-8049(92)90003-k. View

2.
Tang Z, Li C, Kang B, Gao G, Li C, Zhang Z . GEPIA: a web server for cancer and normal gene expression profiling and interactive analyses. Nucleic Acids Res. 2017; 45(W1):W98-W102. PMC: 5570223. DOI: 10.1093/nar/gkx247. View

3.
Adler A, Chang H . From description to causality: mechanisms of gene expression signatures in cancer. Cell Cycle. 2006; 5(11):1148-51. DOI: 10.4161/cc.5.11.2798. View

4.
Phipps C, Lee Y, Ying H, Nagarajan C, Grigoropoulos N, Chen Y . The impact of time from diagnosis to treatment in diffuse large B-cell lymphoma. Leuk Lymphoma. 2018; 59(10):2336-2341. DOI: 10.1080/10428194.2017.1422863. View

5.
Liu R, Cheng Y, Yu J, Lv Q, Zhou H . Identification and validation of gene module associated with lung cancer through coexpression network analysis. Gene. 2015; 563(1):56-62. DOI: 10.1016/j.gene.2015.03.008. View