Heparanase Gene Hypomethylation as a Potential Biomarker for Precision Screening of Bladder Cancer

Bai-sheng Xu, Yan-ying Jiang, Caizhi Liao, M. Yan
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引用次数: 5

Abstract

Background: Epigenetics has been playing an increasingly important role in the study of the origin and development of bladder cancer (BC). This study aimed to investigate the correlation between promoter hypomethylation of the heparanase (HPSE) gene and clinicopathologic characteristics of bladder cancer (BC). Materials and Methods: The promoter hypomethylation profile was evaluated by methylation-specific polymerase chain reaction (PCR) using 27 BC tissue specimens and 15 normal control specimens. The aim was to help decipher the underlying relationship between the clinicopathologic characteristics and the hypomethylation status. Results: Experimental results showed that 16 (59.26%) BC specimens demonstrated the promoter hypomethylation of HPSE, including 2 cases with complete demethylation. For normal control groups, only 3 specimens (20%) indicated hypomethylation (P<0.05). In addition, the occurrence of hypomethylation increased with the metastasis of positive lymph nodes (P<0.05). Importantly, no significant correlation was found between the hypomethylation of HPSE and the profile of patients including gender, age, tumor size, cancer stage, or histologic grade (P>0.05). Conclusion: The promoter hypomethylation of HPSE gene is a common epigenetic event occurring in BC and is positively correlated with a poor prognosis. This study suggested that the promoter hypomethylation could be used as a potential biological marker for the early screening of BC.
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肝素酶基因低甲基化作为精确筛选膀胱癌的潜在生物标志物
背景:表观遗传学在膀胱癌(BC)发生发展的研究中发挥着越来越重要的作用。本研究旨在探讨肝素酶(HPSE)基因启动子低甲基化与膀胱癌(BC)临床病理特征的相关性。材料和方法:采用甲基化特异性聚合酶链反应(PCR)对27例BC组织标本和15例正常对照标本的启动子低甲基化谱进行评估。目的是帮助破译临床病理特征和低甲基化状态之间的潜在关系。结果:16例(59.26%)BC标本显示HPSE启动子低甲基化,其中2例完全去甲基化。正常对照组只有3例(20%)出现低甲基化(P0.05)。结论:HPSE基因启动子低甲基化是BC常见的表观遗传事件,与预后不良呈正相关。本研究提示,启动子低甲基化可作为早期筛查BC的潜在生物学标志物。
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