共 59 条
Role of claudins in tumorigenesis
被引:207
作者:

Swisshelm, K
论文数: 0 引用数: 0
h-index: 0
机构: Univ Washington, Dept Pathol, Seattle, WA 98195 USA

Macek, R
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h-index: 0
机构: Univ Washington, Dept Pathol, Seattle, WA 98195 USA

Kubbies, M
论文数: 0 引用数: 0
h-index: 0
机构: Univ Washington, Dept Pathol, Seattle, WA 98195 USA
机构:
[1] Univ Washington, Dept Pathol, Seattle, WA 98195 USA
[2] Roche Diagnost GmbH, Dept Cell Biol, D-82377 Penzberg, Germany
关键词:
neoplasia;
tight junctions;
signaling pathways;
tumor suppression;
enterotoxin;
D O I:
10.1016/j.addr.2005.01.006
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
The family of more than 20 claudin (CLDN) proteins comprises one of the major structural elements within the apical tight junction apparatus, a dynamic cellular nexus for maintenance of a luminal barrier, paracellular transport, and signal transduction. Loss of normal tight junction functions constitutes a hallmark of human carcinomas. CLDN I may support tumor suppressive functions in tissues such as the brain, where dramatic loss of expression has been demonstrated in glioblastoma multiforme. The role(s) for CLDNs 3 and 4 in tumorigenesis is less clear. CLDN4 appears to be over-expressed in ovarian and pancreatic carcinomas, and this raises the possibility that a unique, potentially non-toxic cancer cell target may be developed through the design of enterotoxin analogues. Future goals include understanding the biochemical and physiological mechanisms that are perturbed as a consequence of CLDN alterations in the progression of solid tumors. (c) 2005 Elsevier B.V. All rights reserved.
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页码:919 / 928
页数:10
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