Immunohistochemical Expression of 14-3-3 σ Protein in Intraductal Papillary-mucinous Tumor and Invasive Ductal Carcinoma of the Pancreas

Background: 14-3-3 σ (sigma) has been shown to be overexpressed in pancreatic cancers by a c-DNA microarray technique. However, the expression of 14-3-3 σ in intraductal papillary-mucinous tumor (IPMT) of the pancreas remains unclear. Materials and Methods: To evaluate the biological importance of...

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Published inAnticancer research Vol. 26; no. 4B; p. 3105
Main Authors TOSHIYUKI OKADA, NORIHIRO MASUDA, YASUYUKI FUKAI, TATSUO SHIMURA, YASUJI NISHIDA, YASUO HOSOUCHI, KENJI KASHIWABARA, TAKASHI NAKAJIMA, HIROYUKI KUWANO
Format Journal Article
LanguageEnglish
Published International Institute of Anticancer Research 01.07.2006
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Summary:Background: 14-3-3 σ (sigma) has been shown to be overexpressed in pancreatic cancers by a c-DNA microarray technique. However, the expression of 14-3-3 σ in intraductal papillary-mucinous tumor (IPMT) of the pancreas remains unclear. Materials and Methods: To evaluate the biological importance of 14-3-3 σ expression in pancreatic carcinogenesis, immunohistochemistry for 14-3-3 σ, CDX2, MUC1, MUC2, p53, p16 and Ki-67 was carried out on 33 IPMTs and the results were compared with those for 14 invasive ductal carcinomas (IDCs). Results: The frequency of 14-3-3 σ immunoreactivity was 70% and 100% in IPMT and IDC, respectively. The frequency of MUC1 and Ki-67 immunoreactivity was significantly higher in IDC than IPMT. In IPMT, dark columnar cell types prevailed over clear columnar cell types in terms of the frequency of the Ki-67 labeling index. Conclusion: The overexpression of 14-3-3 σ was confirmed in both IDC and IPMT. Therefore, this overexpression might occur in the early stages of pancreatic carcinogenesis. Moreover, IPMT composed of dark columnar cells might be a potentially more advanced form than that made up of clear columnar cells.
ISSN:0250-7005
1791-7530