Target intelligence / Profile preview

Protein phosphatase 2A 55 kDa regulatory subunit B gamma isoform (PPP2R2C)

Target
PPP2R2C
Molecular classification
Enzyme regulator, Regulatory subunit, Serine/threonine phosphatase complex component, B55 family of PP2A regulatory subunits
01

Overview

Protein phosphatase 2A 55 kDa regulatory subunit B gamma isoform (PPP2R2C) is a regulatory subunit of the serine/threonine phosphatase PP2A enzyme complex. PPP2R2C encodes the gamma isoform of the B55 (PR55) family. PP2A is a key negative regulator of cell growth and division, controlling phosphorylation states of many critical signaling molecules. The B regulatory subunits, including PPP2R2C, influence both substrate specificity and subcellular localization of PP2A holoenzymes. While PPP2R2C and its family members are structurally similar, they are expressed in distinct tissues and developmental stages, particularly modulating neuronal differentiation and signal transduction pathways such as the MAPK cascade. PPP2R2C and the PP2A complex are implicated in tumor suppression and have roles in neurodegenerative diseases, but as of now, there are no therapies that specifically target PPP2R2C in clinical practice; modulating PP2A broadly remains a frontier of drug development with substantial challenges in selectivity and safety[1][3][4].

Other names
PP2A subunit B gammaPR55B gammaB55gammaPR52IMYPNOIMYPNO1MGC33570PR55GPP2A regulatory subunit B gammaPhosphoprotein phosphatase 2A BR gamma regulatory chain
02

Mechanism of action

Drugs that modulate PP2A generally act by activating or inhibiting phosphatase activity, leading to altered dephosphorylation of oncogenic or neurodegenerative signaling pathways[1]. Selective modulation of substrate specificity or localization via regulatory B subunits (such as PPP2R2C) is a potential future strategy but currently lacks approved agents.

03

Biological functions

Regulation of cell growth and divisionSubstrate specificity modulation of PP2ACellular signal transductionCell cycle regulationModulation of neuronal differentiation (via MAPK cascade)Potential tumor suppressor function (as part of PP2A complex)Apoptosis
04

Disease associations

Cancer (tumor suppressor functions via PP2A)[4]Neurodegenerative disease (role in Alzheimer's and Parkinson's disease as part of PP2A complex)[1]Autism spectrum disorder (as indicated by genetic association)[3]Inflammatory bowel disease[3]
05

Safety considerations

Targeting PP2A holoenzymes can produce on-target toxicity due to the enzyme's broad substrate specificity and central role in diverse cellular pathways[1].Modulation of PPP2R2C might impact cell cycle and apoptosis widely, raising concerns for potential cytotoxicity in normal tissues[1].Lack of subunit or tissue specificity with existing PP2A-targeting drugs limits therapeutic window.
06

Interacting drugs

No specific approved drugs are known to selectively target PPP2R2C to date, but modulators of PP2A activity (such as FTY720/fingolimod, rubratoxin A, and okadaic acid) do affect PP2A holoenzymes as a class, not specific for this regulatory subunit[1].

1 more in the full profile.

07

Biomarkers

Somatic alterations/mutations of PPP2R2C in tumor tissue (potential diagnostics/prognostics under research, not established in clinical use)[4].Dysregulation or altered expression may be relevant in cancer or some neuropsychiatric diseases, although no validated clinical biomarkers for PPP2R2C use are established.

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