Target intelligence / Profile preview

Zinc finger protein 501 (ZNF501)

Target
ZNF501
Molecular classification
Transcription factor, C2H2-type zinc finger protein
01

Overview

Zinc finger protein 501 (ZNF501) is a member of the C2H2-type zinc finger transcription factor family, the largest family of sequence-specific DNA-binding proteins in humans[1][2][4][5]. ZNF501 binds to double-stranded DNA and is involved in the regulation of gene expression in the nucleus, as well as being implicated in the structural integrity of the Golgi apparatus[5]. Though its broad physiological roles are not fully delineated, ZNF501 mutations are associated with neurodevelopmental and neurodegenerative disorders such as autosomal dominant intellectual developmental disorder and frontotemporal dementia/amyotrophic lateral sclerosis[5]. Recent evidence also links ZNF501 to glioblastoma biology, where it supports tumor cell growth and stemness by maintaining the expression of Frizzled class receptor 6 (FZD6) and non-canonical Wnt signaling; silencing ZNF501 sensitizes glioblastoma cells to the chemotherapeutic agent temozolomide[3]. No currently approved drugs specifically target ZNF501, and its potential as a therapeutic target remains exploratory.

Other names
ZNF52MGC21738Zinc finger protein 52ZNFzinc finger protein 52
02

Mechanism of action

Likely involves modulation of gene expression, with observed drug sensitivity change upon ZNF501 ablation influencing glioblastoma cell response to temozolomide[3]

03

Biological functions

Transcriptional regulationGolgi organizationDNA binding
04

Disease associations

Intellectual developmental disorderFrontotemporal dementiaAmyotrophic lateral sclerosisCancer (glioblastoma growth and stemness)
05

Safety considerations

None specifically noted as druggable or associated with known adverse drug safety profiles (general to transcription factors: possible pleiotropy and off-target effects when inhibited or overexpressed)
06

Interacting drugs

Temozolomide
07

Biomarkers

Possibly ZNF501 expression for glioblastoma stemness and/or temozolomide sensitivity (emerging, not widely validated)[3]

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