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Prognostic Impact of Hyaluronan and Its Regulators in Pancreatic Ductal Adenocarcinoma
Author(s) -
Xiaobo Cheng,
Norihiro Sato,
Shiro Kohi,
Koji Yamaguchi
Publication year - 2013
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0080765
Subject(s) - hazard ratio , stroma , medicine , immunohistochemistry , pancreatic cancer , confidence interval , pancreatic ductal adenocarcinoma , oncology , adenocarcinoma , stage (stratigraphy) , multivariate analysis , univariate analysis , gastroenterology , cancer , biology , pathology , paleontology
Background Although pancreatic ductal adenocarcinoma is characterized by an abundant stroma enriched with hyaluronan (HA), the prognostic impact of HA and its regulators remains unknown. Methods Using immunohistochemistry, expression patterns of HA and its regulators, including a synthesizing enzyme (HAS2), and a degrading enzyme (HYAL1) were investigated in patients who received surgical resection. The prognostic significance of these markers and other clinicopathological variables was determined using univariate and multivariate analyses. The HA levels were determined quantitatively by enzyme-linked immunosorbent assay (ELISA). Results We found that strong expressions of HA (P=0.008) and HAS2 (P=0.022) were significantly associated with shorter survival time after surgery. By contrast, weak expression of HYAL1 was significantly associated with poor survival (P=0.001). In multivariate analysis, tumor stage (hazard ratio (HR)=2.76, 95% confidence interval (CI): 1.14-6.66 P=0.024), strong HA expression (HR=6.04, 95%CI: 1.42-25.69 P=0.015), and weak HYAL1 expression (HR=3.16, 95%CI: 1.19-8.40 P=0.021) were independent factors predicting poor survival. ELISA revealed higher concentration of HA in pancreatic cancer tissues than in normal pancreatic tissues (P=0.001). Conclusion These findings suggest, for the first time, that HA and its regulators may have prognostic impact in patients with pancreatic cancer.

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