4.4 Article

A Bioinformatic Analysis: The Overexpression and Prognostic Potential of GPX7 in Lower-Grade Glioma

期刊

INTERNATIONAL JOURNAL OF GENERAL MEDICINE
卷 15, 期 -, 页码 4321-4337

出版社

DOVE MEDICAL PRESS LTD
DOI: 10.2147/IJGM.S356850

关键词

GPX7; pan-cancer; gene expression; prognosis; biomarker

资金

  1. Special R&D Program Project of Chinese Academy of Se-enriched Industry [2020FXZX05-01]
  2. Key Research and Development Program of Shaanxi Province [2020SF-076]
  3. Health Commission of Shaanxi Provincial Government [2018A017]
  4. Education Department of Shaanxi Provincial Government [19JS015]
  5. Subject Invovation Team of Shaanxi University of Chinese Medicine [132041933]

向作者/读者索取更多资源

The study revealed that glutathione peroxidase-7 (GPX7) is overexpressed in multiple tumors and is associated with poor prognosis in lower-grade glioma (LGG) patients. Furthermore, high expression of GPX7 can predict the sensitivity of LGG patients to temozolomide (TMZ).
Purpose: Glutathione peroxidase-7 (GPX7) is a newly discovered non-selenium-containing protein with glutathione peroxidase activity, which mainly protects the organism from oxidative damage and is very important for basic biology studies. This study aims to reveal the expression pattern of GPX7 and its prognosis potential from a pan-cancer perspective. Methods: Expression levels of GPX7 in human tumor tissues and normal tissues were evaluated using Human Protein Atlas (HPA), the Cancer Genome Atlas (TCGA), Genotype-Tissue Expression (GTEx) and UALCAN databases. The prognostic potential of GPX7 for 33 TCGA tumors was evaluated by Kaplan-Meier analysis and Cox regression analysis. Subsequently, the Chinese Glioma Genome Atlas (CGGA) dataset was used to further verify the expression of GPX7 and its prognostic potential in glioma. We explored the correlation between GPX7 and immune infiltration, tumor mutational burden (TMB) and microsatellite instability (MSI). Furthermore, a nomogram lower-grade glioma (LGG) was constructed to verify the prognostic outcome of patients. Finally, the relationship between GPX7 and treatment regimens for LGG was also explored. Results: GPX7 was overexpressed in multiple tumors. Elevated expression of GPX7 was associated with poor prognosis of LGG patients (OS hazard ratio (FIR) = 1.044, P < 0.0001; DFS HR = 1.035, P < 0.0001; PFS HR = 1.045, P < 0.0001). GPX7 was proved to be an independent prognostic factor of LGG through univariate and multivariate Cox analysis. The nomogram confirmed a better predictability (Concordance index (C-index): 0.845; 95% CI, 0.825-0.865). GPX7 was positively correlated with TMB in LGG. GPX7 expression was negatively correlated with half-maximal inhibitory concentration (IC50) of temozolomide (TMZ) (<(rho)over cap> (spearm)(an)= -0.59, P =1.3e-48). Conclusion: GPX7 was upregulated in multiple tumors, and it was a potential prognostic biomarker in LGG. High-expressed GPX7 can predict the sensitivity of TMZ in LGG patients.

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