Target intelligence / Profile preview

PR domain zinc finger protein 4 (PRDM4)

Target
PRDM4
Molecular classification
Transcription factor, Histone modification mediator (via recruitment of protein arginine methyltransferase), PR-domain zinc finger protein family
01

Overview

PR domain zinc finger protein 4 (PRDM4) is a transcription factor in the PR-domain family, characterized by one PR domain and multiple zinc finger motifs. It regulates cell proliferation, self-renewal, and differentiation—critical in development and tumorigenesis. PRDM4 acts mainly as a tumor suppressor in certain cancers (e.g., cervical, gastric) by inducing cell cycle arrest and inhibiting the PI3K/AKT signaling pathway through direct transactivation of PTEN, but may promote invasion/metastasis in other tissues (e.g., pancreatic cancer). It also recruits protein arginine methyltransferase 5 (PRMT5), mediating histone arginine methylation essential for transcriptional regulation. PRDM4’s variable functions reflect complex control of gene expression and cell fate in both normal development and disease contexts. No approved drugs directly target PRDM4; its role as a biomarker and therapeutic target is still under investigation, and its diverse, tissue-specific functions require careful therapeutic consideration.

Other names
PR/SET domain 4PR domain-containing protein 4PFM1PR-domain zinc-finger protein PFM1PR domain 4PR domain containing 4
02

Mechanism of action

Drugs/compounds that modulate PRDM4 affect the PI3K/AKT pathway via PTEN transactivation; this, in turn, regulates cell proliferation and tumorigenicity Experimental silencing and activation approaches used in cancer cell models

03

Biological functions

Cell proliferationCell differentiationStem cell self-renewalTumorigenesisSignal transductionRegulation of cell cycleHistone arginine methylation
04

Disease associations

Cancer (inhibiting proliferation and tumorigenesis in cervical and gastric cancer, promoting invasion/metastasis in pancreatic cancer)Porokeratosis (GeneCards association)Obesity/diabetes (energy expenditure and insulin resistance in mouse studies)Potential roles in other tissue-specific diseases (based on transcriptional regulation and cancer association)
05

Safety considerations

No direct clinical safety concerns for drugs targeting PRDM4 reportedTherapeutic challenge includes tissue-specific and heterogenous roles (tumor suppressor in some cancers, promoter in others), which may complicate targeting
06

Interacting drugs

PTEN inhibitor SP1670 (used experimentally to study PRDM4 function, not a clinical drug targeting PRDM4)

1 more in the full profile.

07

Biomarkers

PRDM4 expression (downregulated in certain cancers, e.g., cervical cancer; associated with prognosis in gastric cancer)PTEN expression (as a downstream biomarker of PRDM4 activity in experimental studies)Ki67 (as an indicator of proliferation in PRDM4-related experiments)

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