Target intelligence / Profile preview

Myotubularin-related protein 7 (MTMR7)

Target
MTMR7
Molecular classification
Enzyme, Lipid phosphatase, Protein tyrosine phosphatase, Member of the Myotubularin family
01

Overview

Myotubularin-related protein 7 (MTMR7) is a 75–76 kDa dual-specificity lipid phosphatase primarily expressed in brain, liver, kidney, and testis. It dephosphorylates phosphatidylinositol 3-phosphate and inositol 1,3-bisphosphate, influencing intracellular signaling cascades crucial for cell growth, proliferation, and metabolism. MTMR7 interacts with proteins such as MTMR9 and PPARγ, modulating their activity in processes like insulin signaling and cellular differentiation. Its expression is reduced in colorectal cancer, making it a candidate biomarker and therapeutic target for metabolic and oncologic diseases. Key domain features: MTMR7 contains a plextrin homology (PH) domain, protein tyrosine phosphatase (PTP) region, SET-interaction (SID) domain, and a coiled-coil (CC) domain that mediates protein-protein interactions. Note: No direct approved drugs targeting MTMR7 are listed in current databases, but several studies propose its role as a novel drug target in cancer and metabolic disease contexts.

Other names
MTMR7Phosphatidylinositol-3-phosphate phosphatase MTMR7
02

Mechanism of action

MTMR7 functions through the inhibition of insulin-mediated AKT-ERK1/2 signaling by lowering phosphoinositide levels. It also activates PPARγ via complex formation and inhibition of ERK1/2-dependent phosphorylation. Its primary enzymatic action involves dephosphorylation at the D-3 position of lipid and soluble substrates.

03

Biological functions

Dephosphorylation of phosphatidylinositol 3-phosphate (PtdIns(3)P) and inositol 1,3-bisphosphate (Ins(1,3)P2)Regulation of insulin signaling via inhibition of AKT-ERK1/2 pathwayModulation of peroxisome proliferator-activated receptor gamma (PPARγ) activityControl of cell proliferation and signal transduction
04

Disease associations

Cancer (notably colorectal cancer)Myopathy, centronuclear, type 6Combined oxidative phosphorylation deficiency 8Potential links to metabolic disease (Type 2 diabetes)
05

Safety considerations

Down-regulation linked to cancer progressionPossible challenges with targeting phosphatases due to broad signaling roles and tissue distribution
06

Interacting drugs

No specific approved drugs are listed as direct interactors, but MTMR7 is highlighted as a potential drug target for cancer and metabolic disease.

1 more in the full profile.

07

Biomarkers

Loss of MTMR7 expression in colorectal tumors (potentially predictive for prognosis)Presence in stromal regions associated with poor colorectal cancer prognosis

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