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Hypermethylation-mediated reduction of WWOX expression in intraductal papillary mucinous neoplasms of the pancreas

机译:高甲基化介导的胰腺导管内乳头状黏液性肿瘤中WWOX表达的降低

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摘要

We have previously shown that WW domain-containing oxidoreductase (WWOX) has tumour-suppressing effects and that its expression is frequently reduced in pancreatic carcinoma. In this study, we examined WWOX expression in intraductal papillary mucinous neoplasm of the pancreas (IPMN) to assess the function of WWOX in pancreatic duct tumourigenesis using immunohistochemistry and methylation-specific polymerase chain reaction analysis. Among 41 IPMNs including intraductal papillary mucinous adenomas (IPMAs) and intraductal papillary mucinous carcinomas (IPMCs), loss or reduced WWOX immunoreactivity was detected in 3 (15%) of 20 IPMAs and 17 (81%) of 21 IPMCs. In addition, hypermethylation of the WWOX regulatory site was detected in 1 (33%) of 3 WWOX(−) IPMAs and 9 (53%) of 17 WWOX(−) IPMCs, suggesting that hypermethylation may possibly be important in the suppression of WWOX expression. Reduction of WWOX expression was significantly correlated with a higher Ki-67 labelling index but was not correlated with the ssDNA apoptotic body index. Interestingly, decreased WWOX expression was significantly correlated with loss of SMAD4 expression in these IPMNs. The results indicate that downregulation of WWOX expression by the WWOX regulatory region hypermethylation is critical for transformation of pancreatic duct.
机译:先前我们已经表明,含WW域的氧化还原酶(WWOX)具有肿瘤抑制作用,并且其表达在胰腺癌中经常降低。在这项研究中,我们检查了胰管内乳头状黏液性肿瘤(IPMN)中WWOX的表达,以使用免疫组织化学和甲基化特异性聚合酶链反应分析评估WWOX在胰腺导管肿瘤发生中的功能。在41种IPMN中,包括导管内乳头状黏液腺瘤(IPMA)和导管内乳头状黏液腺癌(IPMC),在20例IPMA中有3例(15%)和21例IPMC中有17例(81%)检测到WWOX免疫反应性降低或降低。此外,在3个WWOX(-)IPMA中有1个(33%)和17个WWOX(-)IPMC中有9个(53%)检测到WWOX调控位点的超甲基化,这表明超甲基化可能在抑制WWOX中很重要表达。 WWOX表达的减少与较高的Ki-67标记指数显着相关,但与ssDNA凋亡小体指数无关。有趣的是,在这些IPMN中,WWOX表达的下降与SMAD4表达的丧失显着相关。结果表明,由WWOX调节区超甲基化对WWOX表达的下调对于胰管的转化至关重要。

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