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Updated: Jan 29, 2026

Direct Protein Delivery to Mammalian Cells Using Cell-permeable Cys2-His2 Zinc-finger Domains
Published on: March 25, 2015
The Zinc Finger Ran-Binding Protein 3 (ZRANB3): An Advanced Perspective
Paride Pelucchi1, Ettore Mosca1, Nika Tomsič2
1Istituto di Tecnologie Biomediche (ITB), Consiglio Nazionale delle Ricerche (CNR), Via Fratelli Cervi 93, 20054 Milano, Italy.
Human ZRANB3 protein is vital for DNA damage tolerance and genome stability, acting as a tumor suppressor. Its altered expression in cancer correlates with poor survival, highlighting its prognostic potential.
Area of Science:
- Molecular Biology
- Genetics
- Cancer Research
Background:
- Human zinc finger Ran-binding protein 3 (ZRANB3) is essential for DNA damage tolerance (DDT).
- ZRANB3 functions in replication fork reversal (RFR) and the p53/Polι pathway, implicating it as a tumor suppressor.
- Deregulation of ZRANB3 in tumors is linked to adverse clinical outcomes.
Purpose of the Study:
- To comprehensively review the gene and protein-level literature on ZRANB3.
- To examine ZRANB3 regulation in cancer development.
- To discuss evidence for ZRANB3's role as a tumor suppressor and prognostic biomarker.
Main Methods:
- Literature review integrating gene and protein data.
- Analysis of ZRANB3's role in DNA damage tolerance and replication fork dynamics.
- Examination of ZRANB3 alterations (mutations, copy number) in cancer.
Main Results:
- ZRANB3 maintains genome stability by preventing DNA damage and restoring fork progression.
- ZRANB3 expression is frequently deregulated in tumors, correlating with poor prognosis.
- The correlation between ZRANB3 mRNA and p53 expression is context-dependent, particularly in p53-mutated cancers.
Conclusions:
- ZRANB3 is a critical tumor suppressor involved in DNA repair pathways.
- Altered ZRANB3 is a significant prognostic biomarker in various cancers.
- Further research into ZRANB3's functions in DNA synthesis and metabolism is warranted.
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