RANBP3L expression is significantly downregulated in 18 cancer types, including liver hepatocellular carcinoma (LIHC), compared to normal tissues . Reduced RANBP3L correlates with:
Loss of RANBP3L induces tumor-like phenotypes in renal epithelial cells, mimicking KIRC morphology and gene expression .
Prognostic gene signatures linked to RANBP3L loss are translatable to human KIRC samples .
In LIHC, RANBP3L expression correlates with immune cell infiltration:
| Immune Cell Type | Correlation with RANBP3L | Impact on Prognosis |
|---|---|---|
| B cells, CD8+ T cells | Positive | Improved OS |
| Macrophages | Negative | Reduced tumor-free survival |
| Neutrophils | Variable | Linked to shorter DSS |
LIHC: High RANBP3L expression predicts better survival, suggesting utility as a prognostic biomarker .
KIRC: RANBP3L loss promotes oncogenic transformation, highlighting its role as a tumor suppressor .
CML Context: While studies focus on the related protein RanBP3, its role in chemosensitivity (e.g., imatinib response) underscores potential parallels for RANBP3L in therapeutic targeting .