Reduced expression of neural cell adhesion molecule induces metastatic dissemination of pancreatic β tumor cells

被引:112
作者
Perl, AK
Dahl, U
Wilgenbus, P
Cremer, H
Semb, H
Christofori, G
机构
[1] Res Inst Mol Pathol, A-1030 Vienna, Austria
[2] Umea Univ, Dept Microbiol, S-90187 Umea, Sweden
[3] Univ Marseille, CNRS,INSERM, IBDM LGPD, Marseille, France
关键词
D O I
10.1038/6502
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
As in the development of many human cancers, in a transgenic mouse model of beta-cell carcinogenesis (Rip1Tag2), expression of neural cell adhesion molecule (NCAM) changes from the 120-kDa isoform in normal tissue to the 140/180-kDa isoforms in tumors. NCAM-deficient Rip1Tag2 mice, generated by crossing Rip1Tag2 mice with NCAM knockout mice, develop metastases, a tumor stage that is not seen in normal Rip1Tag2 mice. In contrast, overexpression of NCAM 120 in NCAM-deficient Rip1Tag2 mice prevents tumor metastasis. The results indicate that the loss of NCAM-mediated cell adhesion is one rate-limiting step in the actual metastatic dissemination of beta tumor cells.
引用
收藏
页码:286 / 291
页数:6
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