Target intelligence / Profile preview

RELT-like protein 1 (RELL1)

Target
RELL1
Molecular classification
Receptor (type I transmembrane protein, though it does not bind classical TNFSF ligands), Member of the RELT family (with RELT and RELL2)
01

Overview

RELT-like protein 1 (RELL1) is a type I transmembrane protein of the RELT family, containing a short extracellular domain and a variable intracellular domain likely important for protein stability and signaling[1][2][4][7]. Although termed a receptor, it lacks the conserved death domain typical of apoptosis-inducing TNFR family members and has not been shown to bind classical TNFSF ligands. RELL1 is expressed nearly ubiquitously, with particular abundance in bone marrow, placenta, and immune tissues[1][4]. It is regulated by interferons and exhibits circadian expression patterns in specific tissues. Functionally, RELL1 participates in activation of the p38 and JNK MAPK signaling cascades, induces apoptosis when overexpressed, inhibits cellular autophagy via mTOR interaction, and has emerging roles in immune modulation, tumor progression, and infection response[1][2][4][7]. While it is not yet a direct therapeutic target, its biology suggests possible relevance for future intervention in cancer, infection, and immune disorders[1][6].

Other names
RELL1RELT-like protein 1PSEC0162receptor expressed in lymphoid tissues like 1tmp_locus_29
02

Mechanism of action

Activation/inhibition of the MAPK14/p38 and JNK signaling pathways Inhibition of autophagy via activation of mTOR

03

Biological functions

Activation of MAPK14/p38 signaling cascadeActivation of JNK MAPK pathwayInduction of apoptosis when overexpressedPositive regulation of p38MAPK pathwayNegative regulation of autophagy via interaction with mTORInvolvement in immune cell signaling (interferon-regulated expression, impacts macrophage and T cell function)
04

Disease associations

Cancer (upregulated in tumor settings, including glioma; circRELL1 RNA implicated in gastric cancer)Infection (regulates macrophage response to Mycobacterium tuberculosis)Inflammation (involved in CNS disease settings via immune signaling)Other (possible roles in circadian gene regulation and autophagy modulation relevant to diverse pathologies)
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Safety considerations

None specifically cited; because RELL1 appears broadly expressed and regulates immune and apoptosis signaling, direct targeting may provoke off-target or pleiotropic effects in multiple tissues
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Interacting drugs

None explicitly reported for direct pharmacological targeting as of current knowledge; roles as an immune and autophagy modulator suggest potential therapeutic interest but no approved drugs or tool compounds are cited
07

Biomarkers

No clinically validated biomarkers for patient selection or efficacy monitoring directly referencing RELL1 as of current sources; circRELL1 RNA (a non-coding transcript) has been studied as a biomarker in gastric cancer research contexts

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