2003
DOI: 10.3892/or.10.1.21
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Differential roles of alterations of p53, p16, and SMAD4 expression in the progression of intraductal papillary-mucinous tumors of the pancreas

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Cited by 45 publications
(37 citation statements)
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“…So far, genetic analyses of IPMN have disclosed abnormalities in many of the same genes altered in conventional ductal adenocarcinoma, including mutations of KRAS [44], TP53/p53 [71], and CDKN2A/p16 genes [72]. In addition, as is true for pancreatic ductal carcinomas, a number of genes, including CDKN2A/p16, may be epigenetically inactivated in IPMN through aberrant DNA methylation [53,54,73,74].…”
Section: Discussionmentioning
confidence: 99%
“…So far, genetic analyses of IPMN have disclosed abnormalities in many of the same genes altered in conventional ductal adenocarcinoma, including mutations of KRAS [44], TP53/p53 [71], and CDKN2A/p16 genes [72]. In addition, as is true for pancreatic ductal carcinomas, a number of genes, including CDKN2A/p16, may be epigenetically inactivated in IPMN through aberrant DNA methylation [53,54,73,74].…”
Section: Discussionmentioning
confidence: 99%
“…Veränderungen im K-ras-Gen wurden mit einer Frequenz von 31% bei IPMN beschrieben [52]. Zudem fanden sich in einem Teil der Fälle ebenso Genmutationen im p16-und im p53-Gen [53,54]. Der Verlust des Tumorsuppressorgens DPC4 scheint nur bei invasiven Komponenten der IPMN vorhanden zu sein und selten aufzutreten [55,56].…”
Section: Molekulargenetische Aspekte Der Ipmnunclassified
“…The prevalence of malignancy in branch-duct IPMN has been observed in up to 20% [13]. The prevalence of invasive carcinoma as reported in MCN varies between 6% and 36% [14][15][16]. A (Table 1).…”
Section: Introductionmentioning
confidence: 99%