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Identification of Epigenetic Interactions between miRNA and Gene Expression as Potential Prognostic Markers in Bladder Cancer.

Amira AwadallaHassan Abol-EneinEman T HamamAsmaa E AhmedSalma M KhirallahAhmed El-AssmySally Abdallah MostafaAhmed O BabalghithMohamed AliMona Abdel-RahimAhmed A ShokeirAhmed M Harraz
Published in: Genes (2022)
Purpose: To identify the role of a set of microRNAs and their target genes and protein expression levels in the pathogenesis of bladder cancer with a muscular invasion (T2-T4) and non-muscular invasion (T1). Methods: In 157 patients, bladder specimen was examined for the expression of a set of miRNAs including let-7a-5p, miRNA-449a-5p, miRNA-145-3P, miRNA-124-3P, miRNA-138-5p, and miRNA-23a-5p and their targeted genes; β-catenin , WNT7A , IRS2 , FZD4 , SOS1 , HDAC1 , HDAC2 , HIF1α , and PTEN using the qRT-PCR technique. The prognostic effect of miRNAs and their targeted genes on cancer-specific survival (CSS) was evaluated in pT2-pT4 stages. Results: pT1 was found in 40 patients while pT2-4 was found in 117 patients. The expression of let-7a-5P, miR-124-3P, miR-449a-5P, and miR-138-5P significantly decreased in pT2-4 compared with pT1 ( p < 0.001), in contrast, miR-23a-5P increased significantly in pT2-pT4 compared with pT1 ( p < 0.001). Moreover, the expression of miR-145 did not show a significant change ( p = 0.31). Higher expression levels of WNT7A , β-catenin , IRS2 , FZD4 , and SOS1 genes were observed in pT2-pT4 compared with pT1, whereas HDAC1 , HDAC2 , HIF1α , and PTEN genes were downregulated in pT2-pT4 compared with pT1. Lower CSS was significantly associated with lower expression of let-7a-5P, miR-124-3P, miR-449a-5P, and miR-138-5P. Higher expression of β-catenin , FZD4 , IRS2 , WNT7a , and SOS1 was significantly associated with worse CSS. In contrast, lower levels of HDAC1 , HDAC2 , HIF1α , and PTEN were associated with lower CSS. Conclusion: Our results support let-7a-5P, miR-124-3P, miR-138-5P, and their target genes can be developed as accurate biomarkers for prognosis in bladder cancer with a muscular invasion.
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