Pioglitazone Induces Dysplastic Urothelial Changes in Urinary Bladder of Experimental Diabetes.

Q3 Medicine
Ahmed A M Abdel-Hamid, Alaa El-Din L Firgany
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引用次数: 0

Abstract

Objectives: Pioglitazone (PIO) is a widely prescribed oral antidiabetic drug that has concerns regarding a potential risk of developing carcinoma of the urinary bladder. The objective of the current study was to assess this potential risk.

Materials and methods: The potential risk of PIO-induced urinary bladder carcinoma was assessed in the current study by examining urinary bladder of rats for urothelial cytokeratin (CK) expression and proliferative activity by Ki67 immunostaining.

Results: Histological examination revealed dysplastic urothelial changes in PIO per se and diabetes mellitus + PIO (diabetic rats receiving PIO). In addition, a significantly (P < 0.05) decreased CK7 and CK8 expression together with a significantly increased CK20 as well as Ki67 expression was detected in the urothelial cells of groups administrated PIO, contrary to those which did not.

Conclusion: The manifestations of urothelial dysplasia evidenced by histological examination as well as by the aberrant expression in CK and Ki67 after PIO administration add supporting evidence at cellular and experimental level to the previous clinical suspicions.

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吡格列酮诱导实验性糖尿病患者膀胱尿路上皮发育不良。
目的:吡格列酮(PIO)是一种广泛使用的口服降糖药,但有潜在的膀胱癌风险。本研究的目的是评估这种潜在风险。材料和方法:本研究通过Ki67免疫染色法检测大鼠膀胱尿路上皮细胞角蛋白(CK)表达和增殖活性,评估pio诱导膀胱癌的潜在风险。结果:组织学检查显示PIO本身和糖尿病+ PIO(接受PIO的糖尿病大鼠)的尿路上皮发育异常。此外,与未给药组相比,给药组尿路上皮细胞CK7和CK8表达显著(P < 0.05)降低,CK20和Ki67表达显著升高。结论:尿路上皮异常增生的组织学表现以及PIO后CK和Ki67的异常表达,为以往的临床怀疑提供了细胞和实验水平的支持证据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.90
自引率
0.00%
发文量
46
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