Immunohistochemical Expression of 14-3-3 Ï Protein in Intraductal Papillary-mucinous Tumor and Invasive Ductal Carcinoma of the Pancreas
Background: 14-3-3 Ï (sigma) has been shown to be overexpressed in pancreatic cancers by a c-DNA microarray technique. However, the expression of 14-3-3 Ï 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 in | Anticancer research Vol. 26; no. 4B; p. 3105 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
International Institute of Anticancer Research
01.07.2006
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Online Access | Get full text |
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Summary: | Background: 14-3-3 Ï (sigma) has been shown to be overexpressed in pancreatic cancers by a c-DNA microarray technique. However,
the expression of 14-3-3 Ï in intraductal papillary-mucinous tumor (IPMT) of the pancreas remains unclear. Materials and Methods:
To evaluate the biological importance of 14-3-3 Ï expression in pancreatic carcinogenesis, immunohistochemistry for 14-3-3
Ï, 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 Ï 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 Ï 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. |
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ISSN: | 0250-7005 1791-7530 |