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

被引:0
作者
Podemska, Edyta [1 ]
Borowczak, Jedrzej [2 ,3 ,4 ]
Lukasik, Damian [1 ]
Grzanka, Dariusz [1 ]
Durslewicz, Justyna [1 ,4 ]
机构
[1] Nicolaus Copernicus Univ Torun, Coll Medicum Bydgoszcz, Dept Clin Pathomorphol, Fac Med, PL-85094 Bydgoszcz, Poland
[2] Nicolaus Copernicus Univ Torun, Fac Med, Dept Oncol & Brachytherapy, Coll Medicum Bydgoszcz, PL-85796 Bydgoszcz, Poland
[3] Franciszek Lukaszczyk Oncol Ctr, Clin Dept Oncol, PL-85796 Bydgoszcz, Poland
[4] Franciszek Lukaszczyk Oncol Ctr, Dept Tumor Pathol, PL-85796 Bydgoszcz, Poland
关键词
MRPL23; clear-cell renal cell carcinoma; immunohistochemistry; patient survival; prognostic biomarker; LNCRNA;
D O I
10.3390/cancers16233909
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: This study aimed to investigate the expression and prognostic significance of the MRPL23 protein and mRNA in clear-cell renal cell carcinoma (ccRCC) and adjacent non-tumorous tissues. The goal was to assess the impact of MRPL23 expression on tumor behavior, progression, and patient outcomes. Methods: Using immunohistochemistry (IHC), MRPL23 protein expression was analyzed in 99 cases of ccRCC and 30 adjacent non-tumorous tissues. mRNA levels were assessed using data from The Cancer Genome Atlas (TCGA). Correlations between MRPL23 expression and clinicopathological features were examined, and survival outcomes were evaluated using Kaplan-Meier survival curves and Cox regression analyses. Results: MRPL23 protein expression was significantly lower in ccRCC tissues compared to normal tissues. In contrast, mRNA levels of MRPL23 were significantly elevated in ccRCC tissues. Expression levels were correlated with clinicopathological features, including gender, tumor grade, pT status, and disease stage, underlining their impact on tumor progression. Elevated MRPL23 protein expression was associated with poorer overall survival (OS) in ccRCC patients and remained an independent prognostic marker for adverse outcomes after adjustment for confounding variables. While high MRPL23 mRNA expression was also linked to worse OS, it did not retain its status as an independent prognostic factor after adjustments. Conclusion: MRPL23 protein expression is a potential independent prognostic biomarker in ccRCC, emphasizing its utility in predicting patient outcomes and potentially guiding therapeutic decisions. These findings highlight the importance of further research into the role of MRPL23 in ccRCC pathogenesis and its potential as a therapeutic target.
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页数:10
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