Target intelligence / Profile preview

Zinc finger and BTB domain-containing protein 4 (ZBTB4)

Target
ZBTB4
Molecular classification
Transcription factor, C2H2 zinc finger protein family, BTB (POZ) domain-containing protein
01

Overview

Zinc finger and BTB domain-containing protein 4 (ZBTB4) is a transcriptional repressor in the POK (POZ and Krüppel) family, characterized by C2H2 zinc finger and BTB/POZ domains[1][2][4][5]. It binds methylated CpG DNA in a sequence-specific manner, recruits co-repressor complexes such as Sin3/histone deacetylases, and suppresses transcription of target genes including key cell cycle regulators (e.g., p21). ZBTB4 functions as a tumor suppressor, restraining proliferation, invasion, and genomic instability in multiple types of cancers. Its activity is post-translationally regulated, and its loss is associated with increased tumorigenesis and genomic instability. Lower ZBTB4 expression correlates with poor clinical prognosis in colorectal, breast, prostate, and Ewing's sarcoma, and may serve as both a therapeutic target and prognostic biomarker[1][2][5]. It is also implicated in inflammatory pathways and as a genetic modifier in neurodegenerative disease onset[1][2].

Other names
KIAA1538KAISO-L1ZNF903KAISO-like zinc finger protein 1zinc finger and BTB domain containing 4
02

Mechanism of action

Drugs or compounds that increase ZBTB4 expression may exert antineoplastic effects by inhibiting transcription of oncogenic targets (e.g., EZH2, survivin) through Sp transcription factor competition or microRNA modulation[1][2].

03

Biological functions

Transcriptional repressionDNA damage responseCell cycle regulationApoptosisNegative regulation of transcription by RNA polymerase IITumor suppressionMaintenance of genomic stability
04

Disease associations

Cancer (breast, prostate, colorectal, Ewing sarcoma)Neurological disease (modification of Alzheimer’s disease onset)Inflammation
05

Safety considerations

None specifically reported for direct targeting; challenges may include off-target effects or impaired cell cycle regulation when interfering with transcriptional repressors, but clinical data are lacking.
06

Interacting drugs

None directly established; some experimental compounds (e.g., CDODA-Me) modulate expression via microRNA pathways but no direct drug-binding reported[2].
07

Biomarkers

ZBTB4 expression as a prognostic biomarker for patient survival in several cancers, particularly colorectal and breast cancer[2].Low expression associated with poor prognosis and metastasis.

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