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pmid:35721499

Integrated Analysis of Glutathione Metabolic Pathway in Pancreatic Cancer.

Xingui Wu · Ruyuan Yu · Meisongzhu Yang · Yameng Hu · Miaoling Tang · Shuxia Zhang · Ainiwaerjiang Abudourousuli · Xincheng Li · Ziwen Li · Xinyi Liao · Yingru Xu · Man Li · Suwen Chen · Wanying Qian · Rongni Feng · Jun Li · Fenjie Li

Frontiers in cell and developmental biology · 2022 doi:10.3389/fcell.2022.896136

Paper

complete

Experiment

complete

Data

partial

Analysis

partial

Execution

absent

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title
Integrated Analysis of Glutathione Metabolic Pathway in Pancreatic Cancer.
doi
10.3389/fcell.2022.896136
pmid
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[0]
Xingui Wu
[1]
Ruyuan Yu
[2]
Meisongzhu Yang
[3]
Yameng Hu
[4]
Miaoling Tang
[5]
Shuxia Zhang
[6]
Ainiwaerjiang Abudourousuli
[7]
Xincheng Li
[8]
Ziwen Li
[9]
Xinyi Liao
[10]
Yingru Xu
[11]
Man Li
[12]
Suwen Chen
[13]
Wanying Qian
[14]
Rongni Feng
[15]
Jun Li
[16]
Fenjie Li
journal
Frontiers in cell and developmental biology
year
2022
abstract
Metabolic enzyme-genes (MEs) play critical roles in various types of cancers. However, MEs have not been systematically and thoroughly studied in pancreatic cancer (PC). Global analysis of MEs in PC will help us to understand PC progressing and provide new insights into PC therapy. In this study, we systematically analyzed RNA sequencing data from The Cancer Genome Atlas (TCGA) (n = 180 + 4) and GSE15471 (n = 36 + 36) and discovered that metabolic pathways are disordered in PC. Co-expression network modules of MEs were constructed using weighted gene co-expression network analysis (WGCNA), which identified two key modules. Both modules revealed that the glutathione signaling pathway is disordered in PC and correlated with PC stages. Notably, glutathione peroxidase 2 (GPX2), an important gene involved in glutathione signaling pathway, is a hub gene of the key modules. Analysis of immune microenvironment components reveals that PC stage is associated with M2 macrophages, the marker gene of which is significantly correlated with GPX2. The results indicated that GPX2 is associated with PC progression, providing new insights for future targeted therapy.
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Whole-Tissue Gene Expression Study of Pancreatic Ductal Adenocarcinoma
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