Claudin-4 Expression Predicts Survival in Pancreatic Ductal Adenocarcinoma
Background Identification of prognostic markers would be useful in the clinical management of patients with pancreatic ductal adenocarcinoma (PDAC). The clinical relevance of claudin-4 (CLDN4), recently identified as overexpressed in PDAC, is unknown. Methods Using quantitative real-time reverse tra...
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Veröffentlicht in: | Annals of surgical oncology 2012-07, Vol.19 (Suppl 3), p.491-499 |
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Hauptverfasser: | , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
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Zusammenfassung: | Background
Identification of prognostic markers would be useful in the clinical management of patients with pancreatic ductal adenocarcinoma (PDAC). The clinical relevance of claudin-4 (CLDN4), recently identified as overexpressed in PDAC, is unknown.
Methods
Using quantitative real-time reverse transcription-polymerase chain reaction (qRT-PCR), we analyzed
CLDN4
mRNA expression in a panel of 9 pancreatic cancer cell lines and formalin-fixed paraffin-embedded (FFPE) tissues from 100 patients with PDAC. The
CLDN4
expression levels were then correlated with clinicopathological variables and patient outcome. We also performed immunohistochemical analysis in 20 FFPE samples of PDAC to investigate the expression of CLDN4 protein.
Results
Increased expression of
CLDN4
was confirmed in all the pancreatic cancer cell lines tested compared with normal ductal epithelial cells and fibroblasts. We found that low expression of
CLDN4
was significantly associated with shorter survival in patients with PDAC (hazard ratio; 1.362, 95% confidence interval; 1.011–1.873,
P
= 0.0419). Patients with high
CLDN4
expression survived longer for a median of 63.0 months, compared with 14.7 months in patients with low
CLDN4
expression (
P
= 0.0067). In immunohistochemical analysis, the level of
CLDN4
mRNA expression was significantly correlated with the expression of CLDN4 protein (
P
= 0.0168).
Conclusion
Increased expression of
CLDN4
mRNA predicts better prognosis in PDAC. |
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ISSN: | 1068-9265 1534-4681 |
DOI: | 10.1245/s10434-011-1970-2 |