Target intelligence / Profile preview

Epithelial membrane protein 1 (EMP1)

Target
EMP1
Molecular classification
Transmembrane protein, Member of the growth arrest-specific 3 (GAS3)/peripheral myelin protein 22 kDa (PMP22) gene family, Four transmembrane domain protein, Related to the tetraspan/transmembrane 4 superfamily (but not a classical tetraspanin)
01

Overview

Epithelial membrane protein 1 (EMP1) is a four-transmembrane-domain protein belonging to the growth arrest-specific 3 (GAS3)/peripheral myelin protein 22 kDa (PMP22) gene family. EMP1 is implicated in key regulatory roles in cell proliferation, cell migration, apoptosis, cell-cell adhesion, and immune microenvironment modulation. In cancer, EMP1 can act both as a promoter of tumor metastasis (such as in prostate cancer and glioblastoma) and as a tumor suppressor (e.g., in nasopharyngeal, esophageal, colorectal, gastric, and ovarian cancers), with its expression variously upregulated or downregulated depending on tumor type and context[1][3][5]. EMP1 may regulate signal transduction and immune cell interactions, affecting tumor immune infiltration. Although no drugs currently target EMP1 clinically, it is under investigation as a novel therapeutic and diagnostic target, and its expression status is proposed as a biomarker for prognosis and tumor immune landscape across multiple tumor types[1][2][3][5].

Other names
B4BTMPEMP-1CL-20Protein B4BTumor-associated membrane protein
02

Mechanism of action

Not applicable; no currently approved drugs. For experimental targeting, mechanisms focus on inhibiting EMP1-mediated cell migration and invasion—potentially via modulation of Rac1, copine-III interaction, or associated signaling pathways (e.g., PI3K/AKT/mTOR, c-myc)

03

Biological functions

Cell migrationCell proliferationRegulation of apoptosisCell-to-cell interactionCell cycle regulationTight junction component in the blood-brain barrierSignal transductionImmune cell infiltration and modulation
04

Disease associations

Cancer (including prostate cancer, glioblastoma, nasopharyngeal carcinoma, esophageal cancer, bladder cancer, breast cancer, non-small cell lung cancer, ovarian cancer, lymphoma, leukemia, sarcoma, melanoma)Cancer metastasis and invasionTumor immune microenvironment modulationPotentially inflammation-related disease (e.g., psoriasis)
05

Safety considerations

No drugs currently approved for clinical use targeting EMP1; therefore, no established drug-specific adverse events.Hypothetical concerns include impact on cell junction integrity, normal cell migration/proliferation, and immune system regulation if EMP1 function is broadly inhibited (inferred from normal roles in tight junctions, neurogenesis, and immune modulation)
06

Interacting drugs

No directly approved or clinical drugs are currently known to specifically target EMP1; ongoing research considers it a putative target in oncology and possibly immunomodulation
07

Biomarkers

EMP1 protein or mRNA overexpression as a prognostic biomarker for poor survival and metastasis in several cancers (notably glioblastoma, prostate cancer, bladder cancer)Reduced EMP1 expression may signify poorer outcomes or more aggressive disease in some epithelial tumors (e.g., colorectal, esophageal, ovarian cancer)Potential marker for immune cell infiltration and tumor microenvironment analyses in specific cancers

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