TY - JOUR
T1 - Analysis of E-, N-cadherin, α-, β-, and γ-catenin expression in human pancreatic carcinoma cell lines
AU - Toyoda, Eiji
AU - Doi, Ryuichiro
AU - Koizumi, Masayuki
AU - Kami, Kazuhiro
AU - Ito, Daisuke
AU - Mori, Tomohiko
AU - Fujimoto, Koji
AU - Nakajima, Sanae
AU - Wada, Michihiko
AU - Imamura, Masayuki
PY - 2005/3
Y1 - 2005/3
N2 - Objectives: Cadherins are cell surface glycoproteins that mediate Ca 2+-dependent, homophilic cell-cell adhesion. The classic cadherins interact with either β-catenin or γ-catenin, which is bound to α-catenin that links the complex to the actin cytoskeleton. It has been reported that alteration in cadherins/catenins function or expression is found in the neoplastic process as a step in metastasis. The aim of this study was to analyze the expressions of E- and N-cadherins and catenins in human pancreatic cancer cell lines. Methods: We examined the expression of cadherins and catenins in 7 human pancreatic cancer cells by RT-PCR, Western blotting, and immunocytochemistry. The interactions between cadherins and β-catenin were assessed by immunoprecipitation. Results: E-cadherin was expressed in all cell lines except for MIAPaCa-2, whereas N-cadherin was expressed in Capan-2, CFPAC-1, BxPC-3, and PANC-1. The α-, β-, and γ-catenins were expressed and cadherins/β-catenin interactions were detected in all cadherin-expressing cells. Immunocytochemical analysis showed membranous expression of cadherins and catenins. Conclusion: The decreased or loss of cadherins and catenins expression could be involved in the tumor progression and metastasis, although these events may occur in in vivo conditions by interaction between cancer cells and extracellular matrices.
AB - Objectives: Cadherins are cell surface glycoproteins that mediate Ca 2+-dependent, homophilic cell-cell adhesion. The classic cadherins interact with either β-catenin or γ-catenin, which is bound to α-catenin that links the complex to the actin cytoskeleton. It has been reported that alteration in cadherins/catenins function or expression is found in the neoplastic process as a step in metastasis. The aim of this study was to analyze the expressions of E- and N-cadherins and catenins in human pancreatic cancer cell lines. Methods: We examined the expression of cadherins and catenins in 7 human pancreatic cancer cells by RT-PCR, Western blotting, and immunocytochemistry. The interactions between cadherins and β-catenin were assessed by immunoprecipitation. Results: E-cadherin was expressed in all cell lines except for MIAPaCa-2, whereas N-cadherin was expressed in Capan-2, CFPAC-1, BxPC-3, and PANC-1. The α-, β-, and γ-catenins were expressed and cadherins/β-catenin interactions were detected in all cadherin-expressing cells. Immunocytochemical analysis showed membranous expression of cadherins and catenins. Conclusion: The decreased or loss of cadherins and catenins expression could be involved in the tumor progression and metastasis, although these events may occur in in vivo conditions by interaction between cancer cells and extracellular matrices.
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U2 - 10.1097/01.mpa.0000148514.69873.85
DO - 10.1097/01.mpa.0000148514.69873.85
M3 - Article
C2 - 15714139
AN - SCOPUS:20044388895
SN - 0885-3177
VL - 30
SP - 168
EP - 173
JO - Pancreas
JF - Pancreas
IS - 2
ER -