Target intelligence / Profile preview

SH2 domain-containing inositol 5'-phosphatase 2 (SHIP2)

Target
SHIP2
Molecular classification
Enzyme (phosphatidylinositol phosphatase), Phosphatase, SH2 domain-containing protein, Inositol 1,4,5-trisphosphate 5-phosphatase family
01

Overview

SH2 domain-containing inositol 5'-phosphatase 2 (SHIP2) is an enzyme encoded by the INPPL1 gene that specifically hydrolyzes the 5-phosphate from phosphatidylinositol-3,4,5-trisphosphate (PIP3), thus negatively regulating the PI3K/AKT signaling pathway. It contains an SH2 domain and participates in diverse biological processes, including insulin signaling, actin cytoskeleton organization, cell cycle control, cell proliferation, mitosis, endocytosis, immune cell signaling, and EGFR turnover. SHIP2 is implicated in human diseases such as cancer (notably breast cancer), metabolic diseases (including obesity and diabetes), and rare bone development syndromes (e.g., opsismodysplasia). Experimental inhibitors of SHIP2 are being developed for research purposes, but no approved therapeutic agents directly target this protein as of now. SHIP2 serves as a biomarker for certain cancers and plays a crucial role in regulating fundamental cellular and physiological processes, with its dysfunction potentially leading to pathological conditions.

Other names
Inositol polyphosphate phosphatase like 1INPPL1SHIP2INPPL-1SH2 domain-containing inositol phosphatase 2SHIP-2Inositol polyphosphate phosphatase-like protein 1Protein 51C51C proteinPhosphatidylinositol 3,4,5-trisphosphate 5-phosphatase 2
02

Mechanism of action

Inhibition of catalytic phosphatase activity, resulting in increased PI3K/AKT signaling and altered cellular processes (adhesion, proliferation, survival). Experimental inhibitors bind to the SHIP2 catalytic domain

03

Biological functions

Signal transduction (negative regulator of PI3K/AKT pathway)Cell cycle regulation (mitotic spindle orientation)Actin cytoskeleton remodelingEndocytosisCell adhesionCell proliferationCell spreadingImmune response modulationEGFR turnover regulationNeuritogenesis
04

Disease associations

Cancer (support of metastatic growth in breast cancer)Obesity (confers resistance to dietary obesity)Bone development disorders (opsismodysplasia, Schneckenbecken dysplasia)Diabetes/insulin resistance (modulation of insulin signaling)Possibly other related metabolic, immune, and developmental diseases
05

Safety considerations

Targeting SHIP2 may disturb insulin signaling and metabolic homeostasisOther adverse effects may emerge due to broad role in cell proliferation and immune response; detailed safety profile remains to be clarified
06

Interacting drugs

Small-molecule SHIP2 inhibitors (experimental compounds as referenced in inhibition studies)

1 more in the full profile.

07

Biomarkers

Breast cancer marker (INPPL1/SHIP2 is a valuable biomarker for breast cancer)

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