Target intelligence / Profile preview

Segment polarity protein dishevelled homolog DVL-3 (DVL3)

Target
DVL3
Molecular classification
Signal transduction adaptor/scaffold protein, Intracellular effector in the Wnt signaling pathway, Planar cell polarity protein, cytoplasmic phosphoprotein
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Overview

Segment polarity protein dishevelled homolog DVL-3 (DVL3) is an intracellular phosphoprotein and a member of the dishevelled family, homologous to Drosophila dishevelled (dsh). DVL3 functions as a key scaffold/adaptor protein in the Wnt signaling pathway, regulating gene transcription, cell polarity, and cytoskeletal dynamics during embryonic development and adult tissue homeostasis. In humans, DVL3 is critically involved in the formation and maintenance of cell-cell junctions, planar cell polarity, and cytoskeletal organization. Mutations in DVL3 are causally linked to autosomal dominant Robinow syndrome, a developmental disorder affecting skeletal, facial, and organ development. Aberrant DVL3 and Wnt pathway activity are implicated in various cancers and tissue regeneration disorders. Experimental manipulation (such as gene knockdown or pharmacological intervention) of DVL3 results in disruption of actin and microtubule networks, tight junctions, and tissue architecture, highlighting both its therapeutic potential and safety concerns

Other names
Dishevelled-3KIAA0208DSH homolog 3DRS3dishevelled 3 (homologous to Drosophila dsh)dishevelled, dsh homolog 3segment polarity protein dishevelled homolog DVL-3
02

Mechanism of action

Disruption/modulation of Wnt signaling (by inhibiting DVL3 scaffold/adaptor function); Blocking cytoskeletal reorganization (e.g., adjudin summary: downregulates DVL3, disrupts actin and microtubule tracks in Sertoli cells, impeding cell junction and spermatogenesis); General: modulation of DVL3 disrupts planar cell polarity, cell proliferation, and cell junction integrity

03

Biological functions

Signal transduction (Wnt pathway, canonical and non-canonical)Cell proliferationCell polarity/planar cell polarityRegulation of cytoskeleton (actin and microtubules)Embryonic developmentCell adhesion and tight junction regulation
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Disease associations

Robinow syndrome, autosomal dominant (developmental syndrome)Cancer (Wnt pathway dysregulation is strongly associated; specific roles for DVL3 in certain cancers have been reported)Potential involvement in tissue regeneration and homeostasis
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Safety considerations

Developmental toxicity (given its role in embryogenesis, inhibition in non-target tissues could impair normal development)Potential for widespread cellular effects due to central role in Wnt signaling and cytoskeletal organizationRisk of impaired fertility (interfering with DVL3 disrupts spermatogenesis in animal models)
06

Interacting drugs

Adjudin

1 more in the full profile.

07

Biomarkers

DVL3 expression levels (used experimentally to assess blood-testis barrier and spermatogenesis impairment, and can be monitored in research studies of Robinow syndrome and cancer)No clinically validated biomarkers for patient selection or therapeutic monitoring specific to DVL3 currently reported in reviewed sources.

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