Expression of fibroblast activation protein in human pancreatic adenocarcinoma and its clinicopathological significance

AIM: To examine fibroblast activation protein (FAP) expression in pancreatic ductal adenocarcinoma (PDAC) and to analyze its relationship with the clinicopathology of PDAC. METHODS: FAP expression was examined in 134 PDAC specimens by immunohistochemistry, and in four pancreatic cancer cell lines (S...

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Published inWorld journal of gastroenterology : WJG Vol. 18; no. 8; pp. 840 - 846
Main Authors Shi, Min, Yu, Dang-Hui, Chen, Ying, Zhao, Chen-Yan, Zhang, Jing, Liu, Qing-Hua, Ni, Can-Rong, Zhu, Ming-Hua
Format Journal Article
LanguageEnglish
Published United States Baishideng Publishing Group Co., Limited 28.02.2012
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Summary:AIM: To examine fibroblast activation protein (FAP) expression in pancreatic ductal adenocarcinoma (PDAC) and to analyze its relationship with the clinicopathology of PDAC. METHODS: FAP expression was examined in 134 PDAC specimens by immunohistochemistry, and in four pancreatic cancer cell lines (SW1990, Miapaca-2, AsPC-1 and BxPC-3) by Western blotting assay. We also analyzed the association between FAP expression in PDAC cells and the clinicopathology of PDAC patients. RESULTS: The results showed that the FAP was expressed in both stromal fibroblast cells (98/134, 73.1%) and carcinoma cells (102/134, 76.1%). All 4 pancreatic cancer cell lines expressed FAP protein at different levels. Protein bands corresponding to the proteolytically active 170-kDa seprase dimer and its88-kDa seprase subunit were identif ied. Higher FAP expression in carcinoma cells was associated with tumor size (P 〈 0.001), fi brotic focus (P = 0.003), perineural invasion (P = 0.009) and worse clinical outcome (P = 0.0085). CONCLUSION: FAP is highly expressed in carcinoma cells and f ibroblasts in PDAC tissues, and its expression is associated with desmoplasia and worse prognosis.
Bibliography:Pancreatic ductal adenocarcinoma; Cancer-associated fibroblasts; Fibroblast activation protein;Prognosis
AIM: To examine fibroblast activation protein (FAP) expression in pancreatic ductal adenocarcinoma (PDAC) and to analyze its relationship with the clinicopathology of PDAC. METHODS: FAP expression was examined in 134 PDAC specimens by immunohistochemistry, and in four pancreatic cancer cell lines (SW1990, Miapaca-2, AsPC-1 and BxPC-3) by Western blotting assay. We also analyzed the association between FAP expression in PDAC cells and the clinicopathology of PDAC patients. RESULTS: The results showed that the FAP was expressed in both stromal fibroblast cells (98/134, 73.1%) and carcinoma cells (102/134, 76.1%). All 4 pancreatic cancer cell lines expressed FAP protein at different levels. Protein bands corresponding to the proteolytically active 170-kDa seprase dimer and its88-kDa seprase subunit were identif ied. Higher FAP expression in carcinoma cells was associated with tumor size (P 〈 0.001), fi brotic focus (P = 0.003), perineural invasion (P = 0.009) and worse clinical outcome (P = 0.0085). CONCLUSION: FAP is highly expressed in carcinoma cells and f ibroblasts in PDAC tissues, and its expression is associated with desmoplasia and worse prognosis.
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Correspondence to: Ming-Hua Zhu, Professor, Department of Pathology, Changhai Hospital, Second Military Medical University, No. 168 of Changhai Road, Shanghai 200433, China. mhzhu2000@hotmail.com
Telephone: +86-21-81873700 Fax: +86-21-81873700
Author contributions: Shi M, Chen Y, Zhao CY, Zhang J, Liu QH and Ni CR designed, performed the research and analyzed the data; Zhu MH designed the research and analyzed the data; and Yu DH wrote the paper.
ISSN:1007-9327
2219-2840
DOI:10.3748/wjg.v18.i8.840