Molecular Biology of the Cell Sign up for new MBC in Press e-TOCs!

Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Kirjavainen, J.
Right arrow Articles by Jalkanen, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kirjavainen, J.
Right arrow Articles by Jalkanen, M.

Translational suppression of syndecan-1 expression in Ha-ras transformed mouse mammary epithelial cells

J Kirjavainen, S Leppa, NE Hynes and M Jalkanen

Department of Medical Biochemistry, University of Turku, Finland.

A cell surface proteoglycan, syndecan-1, has been shown to participate in the maintenance of the epithelial cell morphology. A point mutated activated c-Ha-ras gene under the control of the glucocorticoid inducible MMTV-LTR promoter was transfected into the mouse mammary epithelial cell line, NOG-8. The NOG-8 ras cells were used to study changes in syndecan-1 expression during epithelial transformation. NOG- 8 ras cells, when induced to express Ha-ras, transformed and formed foci in monolayer cultures and colonies in suspension cultures. Expression of syndecan-1 at the cell surface was markedly reduced in cells showing the transformed phenotype. The accumulation of newly synthesized core protein of syndecan-1 was suppressed in these cells, whereas mRNA levels remained unchanged. This novel finding indicates that syndecan-1 expression is translationally suppressed in the Ha-ras- transformed epithelial cells. Hence, syndecan-1 loss during epithelial transformation could take place without altering syndecan gene transcription and, on the other hand, could be one of the critical events involved in malignant transformation.

Volume 4, Issue 8, pp. 849-858, 08/01/1993
Copyright © 1993 by The American Society for Cell Biology




This article has been cited by other articles:


Home page
Arterioscler. Thromb. Vasc. Bio.Home page
J. M. Lemire, S. Potter-Perigo, K. L. Hall, T. N. Wight, and S. M. Schwartz
Distinct Rat Aortic Smooth Muscle Cells Differ in Versican/PG-M Expression
Arterioscler. Thromb. Vasc. Biol., June 1, 1996; 16(6): 821 - 829.
[Abstract] [Full Text]


Home page
J. Cell Sci.Home page
S Leppa, K Vleminckx, F Van Roy, and M Jalkanen
Syndecan-1 expression in mammary epithelial tumor cells is E-cadherin-dependent
J. Cell Sci., January 6, 1996; 109(6): 1393 - 1403.
[Abstract] [PDF]




Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]