ArticleTranslational cancer research2024
Validation of the interaction between PRDX4 and TXNDC5 in gastric cancer and the significance of the
Article in Translational cancer research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
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Who cites it
6 citing papers in PubMed, 7 citations in OpenAlex.
- Correlation of high PRDX4 expression with poor prognosis in patients with ESCA: Bioinformatics andMolecular and clinical oncology · 2026Article
- Combined assessment of stromal tumor infiltrating lymphocytes and tumor peroxiredoxin 4 expression improved prognostic stratification in postoperative pancreatic cancer patients.Diagnostic pathology · 2026Article
- Cellular characteristics of the immune microenvironment of colorectal cancer and progress in immunotherapy research.Annals of medicine · 2025Review
- Bioinformatic Approach to Identify Positive PrognosticInternational journal of molecular sciences · 2025Article
- The Prognostic Value of Lymphocyte-to-Monocyte Ratio for Long-Term Survival After TACE in Intermediate-to-Advanced Hepatocellular Carcinoma.Journal of hepatocellular carcinoma · 2025Article
- Clinical value and molecular role of PRDXs family in prostate cancer.Frontiers in oncology · 2025Article
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Authors and funding
4 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Background: We successfully screened the important interacting protein peroxiredoxin 4 (PRDX4) of thioredoxin domain-containing protein 5 (TXNDC5) in gastric cancer. However, its specific molecular mechanism in gastric cancer remains unclear. This study aimed to verify the interaction between PRDX4 and TXNDC5 protein molecules in gastric cancer and analyze the expression and functional significance of PRDX4 in gastric cancer using bioinformatics methods. Methods: The interaction between TXNDC5 and PRDX4 was verified by the coimmunoprecipitation (co-IP) of the total protein of gastric cancer cells, and tissues with high expressions of TXNDC5. The Human Protein Atlas (HPA) database, UCSC Xena (University of California Santa Cruz xenabrowser) platform, the Kaplan-Meier Plotter platform, and the TIMER (Tumor IMmune Estimation Resource) platform were used to analyze the expression and subcellular localization of the PRDX4 molecule in normal human gastric tissue, the difference in expression between gastric cancer tissue and normal gastric tissue, the relationship between the expression of PRDX4 and survival, its functional significance in gastric cancer cells, and its effect on the tumor immune microenvironment (TIME). Results: The data analysis results showed that the expression of PRDX4 messenger RNA (mRNA) in the gastric cancer tissues was significantly higher than that in the normal tissues (P<0.05). PRDX4 could affect the occurrence and development of tumors by participating in the neutrophil degranulation signaling pathway to regulate tumor immunity. The expression level of PRDX4 has a certain relationship with the TIME; that is, it is mainly negatively correlated with the infiltration of B lymphocytes and CD4 Conclusions: There is an interaction between PRDX4 and TXNDC5 protein molecules in gastric cancer.
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