Literature DB >> 2703275

Differential expression of cell adhesion molecules in variants of K1735 melanoma cells differing in metastatic capacity.

D Linnemann1, A Raz, E Bock.   

Abstract

We have investigated the expression of 2 neural-cell adhesion molecules, NCAM and LI, in K1735-C116 and -MI melanoma cells which differ qualitatively in their metastatic potential, i.e., MI cells are metastatic whereas C116 cells are not. We have found that NCAM in C116 cells are expressed as 2 quantitatively major glycosylated polypeptides with Mr of 145,000 and 120,000 and a minor 190,000 Mr polypeptide, whereas MI cells expressed NCAM as 3 glycosylated polypeptides with MR of 200,000, 140,000 and 120,000. The amount of NCAM in MI cells constituted only 60% of the amount observed in C116 cells. In C116 cells, the 145,000 and 120,000 Mr NCAM polypeptides were sulphated whereas NCAM did not appear to be sulphated in MI cells. No phosphorylation of NCAM in the 2 cell lines was observed. LI was expressed as a phosphorylated glycoprotein with Mr of 210,000 in MI cells whereas no LI expression was observed in C116 cells. LI was not sulphated in MI cells.

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Year:  1989        PMID: 2703275     DOI: 10.1002/ijc.2910430428

Source DB:  PubMed          Journal:  Int J Cancer        ISSN: 0020-7136            Impact factor:   7.396


  18 in total

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Journal:  Mol Biol Cell       Date:  2001-09       Impact factor: 4.138

Review 5.  Are cellular adhesion molecules involved in the metastasis of breast cancer?

Authors:  M Maemura; R B Dickson
Journal:  Breast Cancer Res Treat       Date:  1994       Impact factor: 4.872

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Authors:  R Akeson; R Bernards
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Authors:  S M Brady-Kalnay; E R Boghaert; S Zimmer; R Brackenbury
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9.  The neural cell adhesion molecule L1 potentiates integrin-dependent cell migration to extracellular matrix proteins.

Authors:  Karsten Thelen; Vishram Kedar; Anitha K Panicker; Ralf-Steffen Schmid; Bentley R Midkiff; Patricia F Maness
Journal:  J Neurosci       Date:  2002-06-15       Impact factor: 6.167

10.  Brain metastasis from colorectal cancer.

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Journal:  Int J Colorectal Dis       Date:  2004-08-11       Impact factor: 2.571

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