Target intelligence / Profile preview

Mitochondrial ribosomal protein S23 (MRPS23)

Target
MRPS23
Molecular classification
Ribosomal protein, Mitochondrial ribosomal protein, Structural constituent of ribosome, Other
01

Overview

Mitochondrial ribosomal protein S23 (MRPS23) is a structural component of the small 28S subunit of the mammalian mitochondrial ribosome. Encoded by a nuclear gene, it is imported into mitochondria and is important for mitochondrial protein synthesis, supporting the oxidative phosphorylation that provides most cellular energy. MRPS23 has been implicated in the pathogenesis of several diseases: its overexpression and post-translational modifications enhance proliferation and metastatic potential in breast cancer and glioma, while pathogenic variants cause clinical mitochondrial disorders with defects in oxidative phosphorylation and energy metabolism. MRPS23 has also been proposed as a cancer biomarker and a potential—but currently untargeted—therapeutic target[1][3][6].

Other names
HSPC329CGI-138MRP-S23S23mtmS2328S ribosomal protein S23, mitochondrialCOXPD46mitochondrial small ribosomal subunit protein mS23
02

Mechanism of action

Not well established; would depend on drug and context. (Drugs have not been specifically identified that target MRPS23 directly in the literature reviewed[1][3].)

03

Biological functions

Mitochondrial protein synthesisRibosomal assemblyRegulation of oxidative phosphorylation (OXPHOS)Cell proliferationApoptosisMetabolism of proteinsOther
04

Disease associations

Cancer (notably breast cancer and glioma)Mitochondrial disease (e.g., combined oxidative phosphorylation deficiency 46)Other
05

Safety considerations

Essential for mitochondrial protein synthesis; systemic targeting likely to be toxic.Potential for disruption of cellular energy metabolism and promotion of mitochondrial dysfunction[1][3].
06

Biomarkers

Overexpression is a prognostic biomarker in breast cancer and glioma[1],[6].Copy number alterations associated with luminal breast cancer proliferation[1].Pathogenic variants linked to mitochondrial disease[1][4][5].

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