Periostin deposition in the stroma of invasive and intraductal neoplasms of the pancreas
Periostin deposition in the stroma of invasive and intraductal neoplasms of the pancreas
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DOI:
10.1038/modpathol.2008.77
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发表时间:
2008-08-01
期刊:
影响因子:
7.5
通讯作者:
Fukayama, Masashi
中科院分区:
文献类型:
--
作者:
Fukushima, Noriyoshi;Kikuchi, Yoshinao;Fukayama, Masashi
Desmoplasia is a common feature of infiltrating ductal adenocarcinoma of the pancreas. This process is intricately interacted between the host and neoplastic cells. Recently, by transcriptome analysis, periostin was identified as a significantly highly expressed gene in pancreatic stellate cells. To investigate the characteristics of periostin immunodeposition in pancreatic ductal neoplasms, we performed immunohistochemistry and in situ hybridization, focusing on tumor -stromal cells interactions. Eighty-one surgically resected pancreatic lesions, including 35 pancreatic ductal adenocarcinoma, 26 intraductal papillary-mucinous neoplasms, 11 mucinous cystic neoplasms and 9 chronic pancreatitis, were studied. In all ductal adenocarcinomas, periostin deposition was observed in the stroma around the infiltrating cancer on immunohistochemistry. Cellular stroma of mucinous cystic neoplasm, called 'ovarian-type' stroma, did not show periostin deposition. In chronic pancreatitis, most of the staining patterns of periostin were perilobular and meshwork-like. Periostin gene expression was detected solely in the stromal cells on in situ hybridization. Intraductal papillary-mucinous neoplasms were classified into four groups on the basis of the histological grade, namely, adenoma, non-invasive adenocarcinoma, adenocarcinoma with microscopical invasion and with macroscopically evident invasion. In intraductal papillary-mucinous neoplasm, periostin deposition in the periductal stroma increased in frequency and intensity in adenocarcinoma compared with adenomas (P = 0.014). Furthermore, our results showed that a higher frequency of periostin deposition was correlated with a higher frequency of ` intestinal phenotype' of proliferating epithelium (P = 0.036) and laminin-5 gamma 2 chain expression (P