TY - JOUR
T1 - Expression of the tumor suppressor gene maspin in human pancreatic cancers
AU - Maass, Nicolai
AU - Hojo, Takashi
AU - Ueding, Michael
AU - Lüttges, Jutta
AU - Klöppel, Günter
AU - Jonat, Walter
AU - Nagasaki, Koichi
PY - 2001
Y1 - 2001
N2 - The tumor suppressor gene maspin, a unique member of the serpin superfamily, inhibits cell motility, invasion, and mestastasis in breast and prostate cancers. Maspin is expressed in normal human mammary and prostate epithelial cells but down-regulated during cancer progression. In this study, we analyzed the expression of maspin in various human cancer cells by means of Northern blot and immunohistochemistry. Maspin gene expression proved to be upregulated in pancreatic cancer. Maspin expression was not detected in any of 6 gastric cancers, 4 melanomas, or 6 of 7 breast cancer cell lines examined. In contrast, 5 of 9 pancreatic cancer cell lines showed maspin expression, although maspin expression was not detected in normal pancreatic tissue. Furthermore, maspin was expressed in 23 of 24 tumor specimens obtained from pancreatic cancer patients as well as all high-grade precancerous lesions (PanIN3 and intraductal carcinoma extension). In contrast, no expression was observed in normal and low-grade precancerous lesions. Our results show that maspin is a new factor associated with pancreatic cancer. In addition, the detection of maspin in pancreatic tumor tissues and its lack of expression in all normal pancreatic tissues suggests that maspin may be a useful marker of primary human pancreatic cancer.
AB - The tumor suppressor gene maspin, a unique member of the serpin superfamily, inhibits cell motility, invasion, and mestastasis in breast and prostate cancers. Maspin is expressed in normal human mammary and prostate epithelial cells but down-regulated during cancer progression. In this study, we analyzed the expression of maspin in various human cancer cells by means of Northern blot and immunohistochemistry. Maspin gene expression proved to be upregulated in pancreatic cancer. Maspin expression was not detected in any of 6 gastric cancers, 4 melanomas, or 6 of 7 breast cancer cell lines examined. In contrast, 5 of 9 pancreatic cancer cell lines showed maspin expression, although maspin expression was not detected in normal pancreatic tissue. Furthermore, maspin was expressed in 23 of 24 tumor specimens obtained from pancreatic cancer patients as well as all high-grade precancerous lesions (PanIN3 and intraductal carcinoma extension). In contrast, no expression was observed in normal and low-grade precancerous lesions. Our results show that maspin is a new factor associated with pancreatic cancer. In addition, the detection of maspin in pancreatic tumor tissues and its lack of expression in all normal pancreatic tissues suggests that maspin may be a useful marker of primary human pancreatic cancer.
UR - http://www.scopus.com/inward/record.url?scp=0034896633&partnerID=8YFLogxK
M3 - Article
C2 - 11309327
AN - SCOPUS:0034896633
SN - 1078-0432
VL - 7
SP - 812
EP - 817
JO - Clinical Cancer Research
JF - Clinical Cancer Research
IS - 4
ER -