Target intelligence / Profile preview

Large ribosomal subunit protein uL14 (RPL23)

Target
RPL23
Molecular classification
Ribosomal protein, Structural constituent of ribosome, Universal ribosomal protein uL14 family, Other (not an enzyme, receptor, ion channel, transporter, or transcription factor)
01

Overview

Large ribosomal subunit protein uL14 (RPL23) is a cytoplasmic ribosomal protein that is a structural component of the 60S ribosomal subunit, a core assembly responsible for eukaryotic protein synthesis. RPL23 also binds the 23S/26S ribosomal RNA. Beyond its canonical function in translation, RPL23 has specialized regulatory roles in cellular stress responses — particularly in stabilizing the p53 tumor suppressor by binding and inhibiting MDM2, thus preventing p53 ubiquitination and degradation. This adjunct function links RPL23 to cell cycle control, apoptosis inhibition, and multidrug resistance mechanisms, especially observed in various cancer cells and hematological malignancies. Its expression correlates with disease progression and therapeutic response, making RPL23 both a potential biomarker and a candidate for experimental gene therapy strategies. There are currently no direct small molecule drugs targeting RPL23, and manipulation of this protein poses significant safety concerns due to its essential cellular roles.

Other names
60S ribosomal protein L2360S ribosomal protein L17ribosomal protein L23ribosomal protein L17rpL17uL14RL23L23L17RL23aRpl17a
02

Mechanism of action

Gene therapy approaches: Adenoviral delivery/co-expression of RPL23 with p53 to enhance tumor suppressor response. Chemotherapy modulation: Altered RPL23 expression impacts apoptotic pathways and cell cycle, contributing to multidrug resistance and resistance to apoptosis-inducing agents.

03

Biological functions

Protein synthesis (core ribosomal function)Regulation of p53 tumor suppressor pathway (binds and inhibits MDM2, stabilizes p53)Cell cycle regulation (impacts Miz1 activity and cell cycle inhibitors p15Ink4b and p21Cip1)Apoptotic regulation (modulates apoptosis, affects apoptotic resistance)Promotes multidrug resistance in cancer cellsBiomarker for aggressive cancer phenotypes
04

Disease associations

Cancer (proliferation, multidrug resistance, apoptosis regulation)Myelodysplastic syndrome (apoptosis resistance, disease progression)Diamond-Blackfan anemiaX-linked sideroblastic anemia with ataxia
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Safety considerations

Targeting ribosomal proteins risks affecting core protein synthesis and may lead to cytotoxicity, cell proliferation defects, and impaired cell viabilityModulating RPL23 may have off-target effects impacting fundamental cellular homeostasis, especially in non-cancerous tissues
06

Interacting drugs

No directly approved drugs currently target RPL23, but gene therapy/adenoviral strategies co-expressing RPL23 with p53 are researched for gastric and colorectal cancer

1 more in the full profile.

07

Biomarkers

Elevated RPL23 expression as a biomarker for aggressive tumor phenotypes, multidrug resistance, and poor therapeutic response (e.g., in myelodysplastic syndrome and certain cancers)Might be used for patient stratification and efficacy monitoring in research

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