High Expression of MRPL23 Is Associated with Poor Survival in Clear-Cell Renal Cell Carcinoma

  • 0Department of Clinical Pathomorphology, Faculty of Medicine, Collegium Medicum in Bydgoszcz, Nicolaus Copernicus University in Torun, 85-094 Bydgoszcz, Poland.

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Summary

This summary is machine-generated.

MRPL23 protein is lower in clear-cell renal cell carcinoma (ccRCC) but its elevated expression predicts poor patient survival. This finding highlights MRPL23 as a potential prognostic biomarker for ccRCC outcomes.

Area Of Science

  • Oncology
  • Molecular Biology
  • Biomarker Discovery

Background

  • Clear-cell renal cell carcinoma (ccRCC) is a significant health concern.
  • Understanding the molecular mechanisms driving ccRCC progression is crucial for improving patient outcomes.

Purpose Of The Study

  • To investigate the expression patterns of MRPL23 protein and mRNA in ccRCC.
  • To determine the prognostic value of MRPL23 in ccRCC patients.
  • To assess the correlation between MRPL23 expression and clinicopathological features.

Main Methods

  • Immunohistochemistry (IHC) was used to analyze MRPL23 protein expression in 99 ccRCC and 30 adjacent non-tumorous tissues.
  • MRPL23 mRNA levels were analyzed using The Cancer Genome Atlas (TCGA) database.
  • Kaplan-Meier survival analysis and Cox regression were employed to evaluate survival outcomes.

Main Results

  • MRPL23 protein expression was significantly lower in ccRCC tissues compared to normal tissues, while mRNA levels were elevated.
  • MRPL23 expression correlated with several clinicopathological features, including gender, tumor grade, pT status, and disease stage.
  • Elevated MRPL23 protein expression was associated with poorer overall survival (OS) and served as an independent prognostic marker for adverse outcomes in ccRCC patients.

Conclusions

  • MRPL23 protein expression is a potential independent prognostic biomarker for ccRCC.
  • These findings suggest MRPL23's role in ccRCC pathogenesis and its potential as a therapeutic target.

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