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In Silico Pan-Cancer Analysis Reveals Prognostic Role of the Erythroferrone (ERFE) Gene in Human Malignancies. | LitMetric

AI Article Synopsis

  • The erythroferrone gene, part of the CTRP family, is linked to cancer progression but its specific role is not well understood.
  • Research indicates that ERFE mRNA is overexpressed in 22 types of tumors, affecting prognosis in 11 of them, with notable associations in breast cancer and adrenocortical carcinoma.
  • ERFE’s expression is connected to various cancer-related pathways and immune cell behavior, suggesting it could serve as a useful prognostic biomarker in tumor development.

Article Abstract

The erythroferrone gene (), also termed , belongs to the C1q tumor necrosis factor-related protein (CTRP) family. Despite multiple reports about the involvement of CTRPs in cancer, the role of ERFE in cancer progression is largely unknown. We previously found that was upregulated in erythroid progenitors in myelodysplastic syndromes and strongly predicted overall survival. To understand the potential molecular interactions and identify cues for further functional investigation and the prognostic impact of ERFE in other malignancies, we performed a pan-cancer in silico analysis utilizing the Cancer Genome Atlas datasets. Our analysis shows that the mRNA is significantly overexpressed in 22 tumors and affects the prognosis in 11 cancer types. In certain tumors such as breast cancer and adrenocortical carcinoma, overexpression has been associated with the presence of oncogenic mutations and a higher tumor mutational burden. The expression of is co-regulated with the factors and pathways involved in cancer progression and metastasis, including activated pathways of the cell cycle, extracellular matrix/tumor microenvironment, G protein-coupled receptor, NOTCH, WNT, and PI3 kinase-AKT. Moreover, expression influences intratumoral immune cell infiltration. Conclusively, is aberrantly expressed in pan-cancer and can potentially function as a prognostic biomarker based on its putative functions during tumorigenesis and tumor development.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9864255PMC
http://dx.doi.org/10.3390/ijms24021725DOI Listing

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