AI Article Synopsis

  • CARD14 is a protein linked to inflammatory skin diseases and serves as a scaffold to activate NF-KB, with new research suggesting it may also influence cancer development.* -
  • Analysis of TCGA tumor data revealed increased CARD14 expression in various cancers, correlating with better patient survival rates in sarcoma, lung, cervix, and head and neck cancers.* -
  • The study indicates that CARD14 not only relates to immune cell infiltration, particularly neutrophils, but also plays a role in epithelial development, suggesting its potential as a prognostic biomarker in cancer.*

Article Abstract

Aberrant caspase recruitment domain family member 14 (CARD14) signaling has been strongly associated with inflammatory skin conditions. CARD14 acts as a scaffold protein, ultimately activating the transcription factor NF-KB. Although primarily studied in the context of inflammation, recent research has suggested its potential implications in tumorigenesis. In this study, we gathered The Cancer Genome Atlas (TCGA) tumor data to gauge the involvement of CARD14 in cancer, including genetic alterations, expression patterns, survival correlations, immune cell infiltration and functional interactions across diverse cancer types. We found heightened CARD14 expression in most tumors and there was a significant correlation between CARD14 expression and the prognosis of patients for certain tumors. For instance, patients with higher CARD14 expression had a better prognosis in sarcoma, lung, cervix and head and neck cancers. Moreover, CARD14 expression positively correlated with neutrophil infiltration in most of the cancer types analyzed. Finally, enrichment analysis showed that epithelial development and differentiation pathways were involved in the functional mechanism of CARD14. Our results show that CARD14 may have the potential to become a prognostic biomarker in several cancers, hence, further prospective studies will be required for its validation.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11452207PMC
http://dx.doi.org/10.1038/s41598-024-74565-4DOI Listing

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