Target intelligence / Profile preview

Ring finger protein 144A (RNF144A)

Target
RNF144A
Molecular classification
E3 ubiquitin ligase, RING-between-RING (RBR) family protein
01

Overview

Ring finger protein 144A (RNF144A) is an E3 ubiquitin ligase belonging to the RING-between-RING (RBR) family of ubiquitin ligases, characterized by its ability to catalyze ubiquitin linkages and target specific proteins for proteasomal degradation, including DNA repair and heat shock proteins. It acts as a tumor suppressor, especially in breast cancer, by promoting degradation of oncoproteins such as HSPA2 and DNA repair factors like PARP1 and DNA-PKcs. Its expression is responsive to DNA damage and loss of RNF144A function is associated with increased tumor growth, poor cancer prognosis, and may influence sensitivity to drugs such as PARP inhibitors. RNF144A may also function in innate immunity via regulation of the STING pathway.

Other names
RNF144ARNF144UBCE7IP4hUIP4UIP4ring finger protein 144A
02

Mechanism of action

Promotes ubiquitination and proteasomal degradation of specific substrates (DNA-PKcs, PARP1, HSPA2, RAF1, BMI1); Alters sensitivity to PARP inhibitors by modulating PARP1 protein abundance

03

Biological functions

Ubiquitination (catalyzes transfer of ubiquitin to substrates)Protein degradation (targets proteins for proteasomal degradation)Regulation of DNA repairModulation of apoptosis (promotes apoptosis following DNA damage)Innate immune response regulation (mediates STING1 ubiquitination)
04

Disease associations

Cancer (tumor suppressor function, especially in breast cancer)Neurological disease (related to RBR family; e.g., parkin in Parkinson disease)
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Safety considerations

Limited direct therapeutic targeting; disruption could impair DNA repair, promote tumor progression, or alter cell death pathways
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Interacting drugs

PARP inhibitors (e.g. olaparib; indirectly, via regulation of PARP1 levels)
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Biomarkers

Low RNF144A expression correlates with aggressive breast cancer and poor prognosis; can predict PARP inhibitor sensitivity in breast cancer

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