Target intelligence / Profile preview

CDC42 small effector protein 2 (CDC42SE2)

Target
CDC42SE2
Molecular classification
Other (Small CDC42-binding protein, Effector protein), Signaling adaptor protein
01

Overview

CDC42 small effector protein 2 (CDC42SE2) is a member of the small CDC42-binding effector protein family characterized by a CRIB (Cdc42/Rac interactive-binding) domain. It acts downstream of the small GTPase CDC42—regulating actin cytoskeletal reorganization, actin filament assembly, cell shape, and survival responses to stress such as proteasome inhibition. In immune cells, it helps coordinate F-actin accumulation at the immunological synapse and may be involved in early stages of phagocytosis. Although not itself considered a classical therapeutic target such as a receptor or enzyme, CDC42SE2 can modulate cellular responses to anti-cancer agents and has been implicated in cancer cell resistance. Its function likely involves functioning as a signaling adaptor protein at the plasma membrane, fine-tuning CDC42-driven signaling cascades important for various cellular and disease contexts.

Other names
SPEC2FLJ21967Small effector of CDC42 protein 2non-kinase Cdc42 effector protein SPEC2
02

Mechanism of action

No specific drugs directly target CDC42SE2. Indirect targeting (e.g., knockdown of CDC42SE2) increases sensitivity to proteasome inhibition (bortezomib) in cancer cells, associating its activity with cell survival pathways.

03

Biological functions

Regulation of signal transductionActin cytoskeleton organizationModulation of actin filament assemblyRegulation of cell shape and morphologyInfluencing cell survival, particularly in response to proteasome inhibitory stressF-actin accumulation at the immunological synapse in T-cellsEarly contractile events in phagocytosis in macrophages
04

Disease associations

Cancer (may contribute to chemotherapy resistance, e.g., bortezomib sensitivity in myeloma)Endometrial serous adenocarcinomaSchizophrenia
05

Safety considerations

None specifically described for targeting CDC42SE2, since it is not an established therapeutic target and no drugs are known to specifically inhibit it in clinical use.
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Interacting drugs

bortezomib
07

Biomarkers

No established biomarkers for patient selection or efficacy monitoring directly related to CDC42SE2.Its expression may have potential (not currently confirmed) as a biomarker for sensitivity to proteasome inhibitors in certain cancers.

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