Target intelligence / Profile preview

DEAD-box helicase 24 (DDX24)

Target
DDX24
Molecular classification
Enzyme, RNA helicase, DEAD-box protein family, Nucleic acid-binding protein
01

Overview

DEAD-box helicase 24 (DDX24) is an ATP-dependent RNA helicase belonging to the DEAD-box protein family, characterized by a conserved Asp-Glu-Ala-Asp (DEAD) motif and a RecA-like core domain. DDX24 is implicated in diverse cellular processes involving alteration of RNA secondary structure, including pre-mRNA splicing, translation initiation, and assembly of ribonucleoprotein (RNP) complexes. It plays a critical role in cell proliferation, cell cycle regulation, and DNA repair in vascular smooth muscle cells by binding and stabilizing FANCA mRNA. DDX24 also acts as a negative regulator of innate immune signaling by sequestering RNA away from pattern-recognition receptors, and as an inhibitor of TP53 transcriptional activity, influencing cell growth arrest and senescence. Loss of DDX24 disrupts vascular development and leads to embryonic lethality in mouse models, underscoring its essential function. DDX24 has been linked to cancer, vascular malformations, and infection-related processes, making it an emerging, albeit currently undrugged, therapeutic target.

Other names
ATP-dependent RNA helicase DDX24DEAD box protein 24DEAD (Asp-Glu-Ala-Asp) box helicase 24DEAD (Asp-Glu-Ala-Asp) box polypeptide 24DEAD/H (Asp-Glu-Ala-Asp/His) box polypeptide 24S. cerevisiae CHL1-like helicaseDDX24
02

Mechanism of action

Not explicitly detailed for drugs, but inhibition of DDX24 would likely impair cell proliferation by causing cell cycle arrest, DNA damage, and impaired RNA metabolism. Targeting DDX24 may modulate innate immune responses or influence p53 pathway activity.

03

Biological functions

RNA metabolism (including pre-mRNA splicing, ribosome and spliceosome assembly)Cell cycle regulationInnate immunity (negative regulation of interferon and cytosolic RNA-mediated signaling)DNA damage response (promotes FANCA mRNA stability for DNA repair)Regulation of cell proliferation and vascular developmentInhibitor of TP53-mediated cell growth arrest and senescence
04

Disease associations

Cancer (various roles in tumorigenesis, vascular/malignant transformation, and sarcoma)Autism spectrum disorder (associative evidence)Embryogenesis/vascular malformations (embryonic lethality with vascular defects upon DDX24 deletion)Infection (facilitates HIV-1 replication and may play antiviral roles)
05

Safety considerations

Potential for embryonic lethality or severe vascular defects (essential gene for development)Risk of impaired DNA repair and cell cycle arrest in normal proliferating cells (off-target effects)Could suppress normal innate immune responses or disrupt RNP homeostasis
06

Interacting drugs

None are currently known or clinically established; the molecule is considered a potential but not yet exploited therapeutic target
07

Biomarkers

DDX24 expression (as a marker for VSMC-mediated vascular development and certain cancers)FANCA mRNA levels in context of DNA repair and vascular development

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