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The EGF-CFC family: novel epidermal growth factor-related proteins in development and cancer

Salomon, David S. and Bianco, Caterina and Ebert, A.D. and Khan, N.I. and de Santis, M. and Normanno, Nicola and Wechselberger, C. and Seno, M. and Williams, K and Sanicola, M. and Foley, S. and Gullick, William J. and Persico, G. (2000) The EGF-CFC family: novel epidermal growth factor-related proteins in development and cancer. Endocrine Related Cancer, 7 (4). pp. 199-226. ISSN 1351-0088. (doi:10.1677/erc.0.0070199) (The full text of this publication is not currently available from this repository. You may be able to access a copy if URLs are provided) (KAR id:16610)

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The EGF-CFC gene family encodes a group of structurally related proteins that serve as important competence factors during early embryogenesis in Xenopus, zebrafish, mice and humans. This multigene family consists of Xenopus FRL-1, zebrafish one-eyed-pinhead (oep), mouse cripto (Cr-l) and cryptic, and human cripto (CR-1) and criptin. FRL-1, oep and mouse cripto are essential for the formation of mesoderm and endoderm and for correct establishment of the anterior/posterior axis. In addition, oep and cryptic are important for the establishment of left-right (UR) asymmetry, In zebrafish, there is strong genetic evidence that oep functions as an obligatory cc-factor for the correct signaling of a transforming growth factor-beta (TGF beta)-related gene, nodal, during gastrulation and during UR asymmetry development. Expression of Cr-l and cryptic is extinguished in the embryo after day 8 of gestation except for the developing heart where Cr-l expression is necessary for myocardial development. In the mouse, cryptic is not expressed in adult tissues whereas Cr-l is expressed at a low level in several different tissues including the mammary gland, In the mammary gland, expression of Cr-l in the ductal epithelial cells increases during pregnancy and lactation and immunoreactive and biologically active Cr-l protein can be detected in human milk. Overexpression of Cr-l in mouse mammary epithelial cells can facilitate their in vitro transformation and in vivo these Cr-l-transduced cells produce ductal hyperplasias in the mammary gland. Recombinant mouse or human cripto can enhance cell motility and branching morphogenesis in mammary epithelial cells and in some human tumor cells. These effects are accompanied by an epithelial-mesenchymal transition which is associated with a decrease in beta -catenin function and an increase in vimentin expression. Expression of cripto is increased several-fold in human colon, gastric, pancreatic and lung carcinomas and in a variety of different types of mouse and human breast carcinomas. More importantly, this increase can first be detected in premalignant lesions in some of these tissues. Although a specific receptor for the EGF-CFC proteins has not yet been identified, oep depends upon an activin-type RIIB and RIB receptor system that functions through Smad-e. Mouse and human cripto have been shown to activate a ras/raf/MAP kinase signaling pathway in mammary epithelial cells. Activation of phosphatidylinositol 3-kinase and Akt are also important for the ability of CR-1 to stimulate cell migration and to block lactogenic hormone-induced expression of p-casein and whey acidic protein. In mammary epithelial cells, part of these responses may depend on the ability of CR-1 to transactivate erb B-4 and/or fibroblast growth factor receptor 1 through an src-like tyrosine kinase.

Item Type: Review
DOI/Identification number: 10.1677/erc.0.0070199
Subjects: Q Science
R Medicine > RC Internal medicine > RC254 Neoplasms. Tumors. Oncology
Divisions: Divisions > Division of Natural Sciences > Biosciences
Depositing User: A. Xie
Date Deposited: 26 Jun 2009 10:21 UTC
Last Modified: 09 Mar 2023 11:31 UTC
Resource URI: (The current URI for this page, for reference purposes)

University of Kent Author Information

Gullick, William J..

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