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Protein expression in vesicoureteral reflux: What about children?
Eda Tokat1, Mustafa Özgür Tan2, Serhat Gürocak2
1University of Health Sciences, Ankara Research and Training Hospital, Department of Urology, Ulucanlar caddesi No:89, Ankara 06230, Turkey.
Insights
This study found decreased protein expression of GDNF/RET, PAX2, and FGFR2 genes in children with vesicoureteral reflux (VUR). These protein levels did not correlate with reflux grade or kidney function, suggesting further research is needed.
Area of Science:
- Pediatric Urology
- Developmental Biology
- Molecular Genetics
Background:
- Vesicoureteral reflux (VUR) pathogenesis involves abnormal embryonal ureteric bud development, with several candidate genes implicated.
- The precise molecular mechanisms underlying VUR remain incompletely understood.
Purpose of the Study:
- To investigate the protein expression levels of GDNF/RET, PAX2, and FGFR2 in ureterovesical junction segments from children with VUR.
- To explore potential correlations between these protein expressions and clinical parameters of VUR.
Main Methods:
- Western blot analysis was performed on 28 ureterovesical junction segments from 19 pediatric patients who underwent ureteroneocystostomy for VUR.
- Protein expression of GDNF/RET, PAX2, and FGFR2 was quantified and compared to β-Actin.
Main Results:
- Significantly lower protein expression of FGFR2, PAX2, and RET was observed in VUR patients compared to the control (β-Actin).
- No significant correlations were found between the protein expression levels of these genes and the grade of VUR or differential renal function.
Conclusions:
- Decreased protein expression of GDNF/RET, PAX2, and FGFR2 is associated with VUR in children.
- The expression levels of these proteins do not appear to correlate with clinical VUR severity or renal function.
- Larger prospective studies are warranted to elucidate the role of these proteins in VUR etiopathogenesis.
Purpose:
Pathogenesis of vesicoureteral reflux (VUR) which concerns improper embryonal ureteric bud development still remains controversial, despite current studies have revealed several candidate genes. In this study, we aimed to determine the protein expression of certain genes which might play role in the pathogenesis of VUR, in the resected ureterovesical junction segments.
Methods:
The study group consisted of 19 children; 12(63%) girls, 7(37%) boys who had ureteroneocystostomy (UNC) operation; 3(15.7%) right sided, 7(36.8%) left sided, 9(47.3%) bilateral due to VUR. As a total, 28 ureterovesical junction segments were available for analysis of protein expressions of GDNF/RET, PAX2 and FGFR2 genes by their Western Blot analysis.
Results:
Protein based expressions of FGFR2, PAX2 and RET were significantly lower than β-Actin (p = 0.001, for all proteins). Correlation analyses between grade of reflux and protein expressions revealed no significant relations (p>0.05, for all proteins). When we grouped the patients into 2 groups as high grade (grade 4-5) and low grade reflux (grade 1-3) for convenient analyses, no statistically significant difference was found between groups (p>0.05, for all proteins). Renal units were also grouped according to differential functions (≥40% and <40%) obtained by renal scintigraphy and compared in terms of proteins' expressions. There was also no significant difference between two groups regarding FGFR2, PAX2 and RET band areas (p>0.05, for all proteins).
Conclusion:
Our study revealed decreased protein expressions of GDNF/RET, PAX2 and FGFR2 genes in the patients with VUR. Relation between clinical parameters and expression levels were statistically uncorrelated. Prospective studies of larger sample size are necessary in order to delineate the impact of certain proteins in the etiopathogenesis of VUR.
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