» Articles » PMID: 10651311

N-linked Oligosaccharides and Metastatic Propensity in in Vivo Selected Mouse Mammary Adenocarcinoma Cells

Overview
Specialty Oncology
Date 2000 Jan 29
PMID 10651311
Citations 1
Authors
Affiliations
Soon will be listed here.
Abstract

Studies using metastatic variant selected in vivo from a cloned parental cell line demonstrate that the expression of beta1-6 branched, N-linked carbohydrates and sialic acid were positively associated with in vitro invasiveness and inversely associated with metastatic potential, adherence, and in vivo growth rate. These results suggest that at least within one tumor model, a negative association occurs between metastatic potential and 1-6 branched oligosaccharide expression. In these studies two metastatic variants, Cl-66M1 and Cl-66M2, were selected following serial in vivo passage of Cl-66, a clonal cell line obtained from a mouse mammary adenocarcinoma cell line. The parent cell line and the two metastatic variants were approximately equal in their adherence to fibronectin, laminin, and collagen type IV coated plastic. In contrast, both Cl-66M1 and Cl-66M2 had a significantly increased ability to invade through matrigel invasion chambers and expressed significantly increased levels of beta1-6 branched, N-linked carbohydrates, and sialic acid compared to the clonal parental cell line, Cl-66. Furthermore, the in vivo tumor growth rates of these selected variants were decreased compared to Cl-66 with the longest tumor volume doubling time observed with Cl-66M2.

Citing Articles

Probing the substrate specificity of Golgi alpha-mannosidase II by use of synthetic oligosaccharides and a catalytic nucleophile mutant.

Zhong W, Kuntz D, Ember B, Singh H, Moremen K, Rose D J Am Chem Soc. 2008; 130(28):8975-83.

PMID: 18558690 PMC: 3982601. DOI: 10.1021/ja711248y.

References
1.
Talmadge J, Fidler I . Cancer metastasis is selective or random depending on the parent tumour population. Nature. 1982; 297(5867):593-4. DOI: 10.1038/297593a0. View

2.
Laemmli U . Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970; 227(5259):680-5. DOI: 10.1038/227680a0. View

3.
Vaage J . Metastasizing potentials of mouse mammary tumors and their metastases. Int J Cancer. 1988; 41(6):855-8. DOI: 10.1002/ijc.2910410614. View

4.
Iida J, Meijne A, Knutson J, Furcht L, McCarthy J . Cell surface chondroitin sulfate proteoglycans in tumor cell adhesion, motility and invasion. Semin Cancer Biol. 1996; 7(3):155-62. DOI: 10.1006/scbi.1996.0021. View

5.
Cifone M, Fidler I . Increasing metastatic potential is associated with increasing genetic instability of clones isolated from murine neoplasms. Proc Natl Acad Sci U S A. 1981; 78(11):6949-52. PMC: 349170. DOI: 10.1073/pnas.78.11.6949. View