Target intelligence / Profile preview

High affinity cAMP-specific 3',5'-cyclic phosphodiesterase 7A (PDE7A)

Target
PDE7A
Molecular classification
Enzyme, 3',5'-cyclic nucleotide phosphodiesterase
01

Overview

High affinity cAMP-specific 3',5'-cyclic phosphodiesterase 7A (PDE7A) is an enzyme encoded by the PDE7A gene in humans. It specifically hydrolyzes cAMP—a second messenger involved in diverse signaling pathways, including immune modulation, muscle function, and neuronal signaling[3][8]. PDE7A, along with its closely related isoform PDE7B, belongs to the PDE7 family and shows minimal activity toward cGMP[3]. PDE7A is expressed in various tissues and is being explored as a therapeutic target for neurological, immune, and substance use disorders. Although no PDE7A-targeting drugs are currently approved, selective inhibition of this enzyme is viewed as a promising strategy for modulating cAMP levels with potentially fewer side effects compared to related phosphodiesterases[2][4][6].

Other names
Phosphodiesterase 7AcAMP-specific phosphodiesterase 7AHigh affinity 3',5'-cyclic-AMP phosphodiesterase 7A
02

Mechanism of action

Inhibition of cAMP hydrolysis leading to increased intracellular cAMP Indirect modulation of cAMP–PKA pathway signaling (affecting CREB/ERK downstream signaling)

03

Biological functions

Hydrolysis of cyclic adenosine monophosphate (cAMP)Regulation of intracellular cAMP levelsSignal transductionModulation of T cell function (e.g. cytokine production, proliferation)May play roles in muscle signal transduction
04

Disease associations

Neurological disease (as a potential target for therapy)Respiratory diseaseAlcohol use disorder (AUD), with sex-specific effects in animal modelsImmune disorders (role in T cell function and possible therapeutic modulation)Other: Possible involvement in cancers and endocrine-related diseases (pituitary, thyroid, testes, though specifics are under investigation)
05

Safety considerations

Off-target effects are likely less frequent than with PDE4 inhibitors (notably fewer gastrointestinal side effects)Long-term effects in humans are not yet established, as no approved PDE7A-targeted drugs are on the market
06

Interacting drugs

BRL50481 (selective PDE7A inhibitor used in research)

1 more in the full profile.

07

Biomarkers

Changes in cAMP levels or downstream effectors (such as pCREB, BDNF) may serve as biomarkers of pharmacodynamic response in preclinical studies

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