Target intelligence / Profile preview

MTOR-associated protein MEAK7 (MEAK7)

Target
MEAK7
Molecular classification
MTOR (mechanistic/mammalian target of rapamycin) pathway adaptor protein, Lysosome-associated protein, TLDc-domain protein, V-ATPase-associated regulator, Other (non-enzymatic, non-receptor, non-transporter scaffolding/regulatory protein)
01

Overview

MTOR-associated protein MEAK7 (MEAK7) is a lysosome-associated TLDc-domain-containing regulatory protein that plays a critical role in activating an alternative mTOR signaling pathway in mammalian cells, particularly cancer cells[1][2][3][4]. MEAK7 promotes cellular proliferation and migration by facilitating the recruitment of mTOR to lysosomes, where it interacts with mLST8 but not canonical mTORC1/2 partners, and selectively activates S6K2 and represses 4E-BP1 phosphorylation, driving protein synthesis and cell growth[1][2]. MEAK7 also binds and regulates the V-ATPase proton pump, possibly acting as a signaling adaptor or modulator, although its exact impact on V-ATPase function is not fully established[3][4]. Overexpression of MEAK7 is linked to poor prognosis and therapy resistance in several cancers, suggesting its potential as a therapeutic target and biomarker[2]. There are no drugs or inhibitors directly targeting MEAK7, but the downstream pathway may be susceptible to mTOR pathway inhibitors[2].

Other names
KIAA1609TLDC1mEAK-7TBC/LysM-associated domain-containing protein 1TLD domain-containing protein 1mammalian EAK-7EAK7eak-7 homolog
02

Mechanism of action

Drugs targeting mTOR or downstream effectors (S6K, 4E-BP1) may indirectly impact MEAK7-dependent signaling[2]. No known drugs specifically inhibit or modulate MEAK7 itself.

03

Biological functions

Signal transduction (via alternative mTOR pathway)Cell proliferationCell migrationCancer cell growth and resistance (chemoresistance and radiation resistance)Modulation of V-ATPase-mediated signalingRecruitment of mTOR to lysosomesProtein translation regulation (via S6K2 and 4E-BP1)
04

Disease associations

Cancer (overexpressed and functionally relevant in non-small-cell lung cancer, breast cancer, hepatocellular carcinoma)Other (implicated broadly in cancer cell proliferation and migration)
05

Safety considerations

Lack of selective MEAK7 inhibitors[2].Potential for off-target effects or disruption of normal mTOR physiology, especially autophagy or cell growth[2].Unknown long-term consequences of MEAK7 modulation in humans[2].
06

Interacting drugs

No direct interacting drugs identified in published literature. However, indirect implication of mTOR pathway drugs (e.g., rapamycin analogs) may be relevant[2].
07

Biomarkers

Overexpression of MEAK7 mRNA/protein in cancer (breast, lung, liver) for diagnosis/prognosis[2].Levels of phosphorylated S6K2 and 4E-BP1 as indicators of MEAK7-mediated signaling[1][2].

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