Target intelligence / Profile preview

Active regulator of SIRT1 (RPS19BP1 (also known as AROS))

Target
RPS19BP1 (also known as AROS)
Molecular classification
Other (SIRT1 regulator/co-factor), Ribosome-binding protein, Post-translational modulator
01

Overview

Active regulator of SIRT1 (AROS), also known as RPS19 binding protein 1 (RPS19BP1), is a nuclear protein that functions as a regulator of the NAD⁺-dependent deacetylase SIRT1 by binding directly to SIRT1 outside its catalytic domain and promoting SIRT1’s deacetylase activity[1][2]. AROS modulates downstream SIRT1 targets, especially p53, affecting its acetylation and thereby regulating cell survival, stress response, and apoptosis, particularly in cancer cells[2][3]. It also interacts directly with ribosomal protein S19 and participates in 40S ribosomal subunit biogenesis, further connecting ribosome assembly and protein translation to cell growth and survival processes[3]. AROS’s cancer-specific functions make it a potential target for therapeutic exploration, though it is not yet targeted by any approved drugs[2]. Its role is complex and context-dependent, contributing variably depending on cell type and stress status, particularly with respect to the SIRT1-p53 axis and ribosome function[2][3].

Other names
RPS19 binding protein 1AROSRPS19BP1S19BPFLJ21770MGC5201040S ribosomal protein S19-binding protein 1
02

Mechanism of action

Enhances SIRT1 deacetylase activity by direct binding, Suppresses p53 acetylation in some cell contexts via SIRT1, Promotes cancer cell survival independently of p53 under certain conditions[2][3].

03

Biological functions

Regulation of SIRT1 deacetylase activityPromotion of cancer cell survivalModulation of p53 acetylationRegulation of ribosome biogenesisRegulation of translation
04

Disease associations

CancerTumor cell survival(potentially) Other diseases involving SIRT1 or ribosome dysfunction
05

Safety considerations

No notable direct safety concerns reported; however, targeting AROS may affect ribosome function and SIRT1-mediated survival pathways in both normal and cancer cells[2][3].
06

Interacting drugs

None reported in the literature as direct binders. Drugs affecting SIRT1 pathway (e.g., SIRT1 inhibitors/activators) may functionally intersect, but no direct drug documented for AROS/RPS19BP1 itself[2].
07

Biomarkers

None specific for patient selection or efficacy monitoring[2][3].

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