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A pan-cancer analysis of thioredoxin-interacting protein as an immunological and prognostic biomarker

BACKGROUND: The critical role of thioredoxin-interacting protein (TXNIP) in cellular sulfhydryl redox homeostasis and inflammasome activation is already widely known, however, no pan-cancer analysis is currently available. METHODS: We thus first explored the potential roles of TXNIP across thirty-th...

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Detalles Bibliográficos
Autores principales: Guo, Xuxue, Huang, Mei, Zhang, Haonan, Chen, Qianhui, Hu, Ying, Meng, Yan, Wu, Changjie, Tu, Chenge, Liu, Yongfeng, Li, Aimin, Li, Qingyuan, Zhou, Peirong, Liu, Side
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9288722/
https://www.ncbi.nlm.nih.gov/pubmed/35843949
http://dx.doi.org/10.1186/s12935-022-02639-2
Descripción
Sumario:BACKGROUND: The critical role of thioredoxin-interacting protein (TXNIP) in cellular sulfhydryl redox homeostasis and inflammasome activation is already widely known, however, no pan-cancer analysis is currently available. METHODS: We thus first explored the potential roles of TXNIP across thirty-three tumors mainly based on The Cancer Genome Atlas and Gene Expression Omnibus datasets. RESULTS: TXNIP is lowly expressed in most cancers, and distinct associations exist between TXNIP expression and the prognosis of tumor patients. TXNIP expression was associated with tumor mutational burden, microsatellite instability, mismatch repair genes, tumor infiltrating immune cell abundance as well as cancer-associated fibroblasts. Moreover, ubiquitin mediated proteolysis, protein post-translational modification and other related pathways were involved in the functional mechanisms of TXNIP. CONCLUSIONS: Our first pan-cancer study comprehensively revealed the carcinostatic role of TXNIP across different tumors. And this molecule may be considered as a potential immunological and prognostic biomarker. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12935-022-02639-2.