Literature DB >> 8241570

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

J Kirjavainen1, S Leppä, N E Hynes, M Jalkanen.   

Abstract

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.

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Year:  1993        PMID: 8241570      PMCID: PMC300997          DOI: 10.1091/mbc.4.8.849

Source DB:  PubMed          Journal:  Mol Biol Cell        ISSN: 1059-1524            Impact factor:   4.138


  41 in total

Review 1.  Post-transcriptional steps in the expression of chloroplast genes.

Authors:  J D Rochaix
Journal:  Annu Rev Cell Biol       Date:  1992

2.  Expression of syndecan in transformed mouse keratinocytes.

Authors:  P Inki; M Gomez; M Quintanilla; A Cano; M Jalkanen
Journal:  Lab Invest       Date:  1992-08       Impact factor: 5.662

3.  High resolution two-dimensional electrophoresis of proteins.

Authors:  P H O'Farrell
Journal:  J Biol Chem       Date:  1975-05-25       Impact factor: 5.157

4.  Epimorphin: a mesenchymal protein essential for epithelial morphogenesis.

Authors:  Y Hirai; K Takebe; M Takashina; S Kobayashi; M Takeichi
Journal:  Cell       Date:  1992-05-01       Impact factor: 41.582

5.  Isolation of a transforming sequence from a human bladder carcinoma cell line.

Authors:  C Shih; R A Weinberg
Journal:  Cell       Date:  1982-05       Impact factor: 41.582

6.  Growth factors induce 3T3 cells to express bFGF-binding syndecan.

Authors:  K Elenius; A Määttä; M Salmivirta; M Jalkanen
Journal:  J Biol Chem       Date:  1992-03-25       Impact factor: 5.157

7.  Dual evolutionary origin for the rat genetic sequences of Harvey murine sarcoma virus.

Authors:  R W Ellis; D DeFeo; J M Maryak; H A Young; T Y Shih; E H Chang; D R Lowy; E M Scolnick
Journal:  J Virol       Date:  1980-11       Impact factor: 5.103

8.  Cell surface proteoglycan of mammary epithelial cells. Protease releases a heparan sulfate-rich ectodomain from a putative membrane-anchored domain.

Authors:  A Rapraeger; M Bernfield
Journal:  J Biol Chem       Date:  1985-04-10       Impact factor: 5.157

9.  Basic fibroblast growth factor-syndecan complex at cell surface or immobilized to matrix promotes cell growth.

Authors:  M Salmivirta; J Heino; M Jalkanen
Journal:  J Biol Chem       Date:  1992-09-05       Impact factor: 5.157

10.  Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease.

Authors:  J M Chirgwin; A E Przybyla; R J MacDonald; W J Rutter
Journal:  Biochemistry       Date:  1979-11-27       Impact factor: 3.162

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  3 in total

Review 1.  Syndecans: multifunctional cell-surface co-receptors.

Authors:  D J Carey
Journal:  Biochem J       Date:  1997-10-01       Impact factor: 3.857

2.  Syndecan-1 is up-regulated in ras-transformed intestinal epithelial cells.

Authors:  Z M Wong; B Choo; M Li; D J Carey; D F Cano-Gauci; R N Buick
Journal:  Br J Cancer       Date:  1998-03       Impact factor: 7.640

3.  Syndecan-1 alterations during the tumorigenic progression of human colonic Caco-2 cells induced by human Ha-ras or polyoma middle T oncogenes.

Authors:  P Levy; A Munier; S Baron-Delage; Y Di Gioia; C Gespach; J Capeau; G Cherqui
Journal:  Br J Cancer       Date:  1996-08       Impact factor: 7.640

  3 in total

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