Target intelligence / Profile preview

Glycine-rich extracellular protein 1 (GREP1)

Target
GREP1
Molecular classification
Other (secreted extracellular protein, not a receptor, enzyme, ion channel, transporter, or transcription factor)
01

Overview

Glycine-rich extracellular protein 1 (GREP1) is a secreted, glycine-rich protein encoded by a previously non-canonical open reading frame (ORF G029442). It is highly expressed in human breast cancer and its knockout selectively reduces viability in breast cancer cell lines. GREP1 influences the abundance of the oncogenic cytokine GDF15 in the cancer cell secretome and is associated with reduced patient survival in breast cancer. Mass spectrometry indicates that GREP1 interacts with extracellular matrix proteins such as fibronectin and collagen. GREP1’s biological activity depends on protein translation (not just RNA presence), indicating it is a protein-coding gene rather than a non-coding RNA in cancer contexts. No documented drugs target GREP1 directly. It is considered a novel cancer vulnerability gene and possible therapeutic target[1].

Other names
GREP1Glycine-rich extracellular protein 1LINC00514G029442Long intergenic non-protein coding RNA 514LA16c-380H5.1LA16c-380H5.3
02

Biological functions

Cell viability regulationExtracellular matrix associationModulation of secretome, especially cytokine GDF15
03

Disease associations

Cancer (strongly implicated in breast cancer)Prognostic marker for breast cancer patient survival
04

Safety considerations

Potential off-target effects or toxicity if targeted therapeutically, as the full spectrum of GREP1 physiological roles is not yet establishedSpecificity to select cancer cell lineages (not universal)
05

Biomarkers

GREP1 mRNA expression (prognostic for breast cancer survival)GDF15 cytokine levels, which are modulated by GREP1

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