Jj. Deman et al., REMOVAL OF SIALIC-ACID FROM THE SURFACE OF HUMAN MCF-7 MAMMARY-CANCERCELLS ABOLISHES E-CADHERIN-DEPENDENT CELL-CELL ADHESION IN AN AGGREGATION ASSAY, In vitro cellular & developmental biology. Animal, 31(8), 1995, pp. 633-639
MCF-7 human breast cancer cells express E-cadherin and show, at least
in some circumstances, E-cadherin-dependent cell-cell adhesion (Bracke
et al., 1993). The MCF-7/AZ variant spontaneously displays E-cadherin
-dependent fast aggregation; in the MCF-7/6 variant, E-cadherin appear
ed not to be spontaneously functional in the conditions of the fast ag
gregation assay, but function could be induced by incubation of the su
spended cells in the presence of insulinlike growth factor I (IGF-I) (
Bracke et al., 1993). E-cadherin from MCF-7 cells was shown to contain
sialic acid. Treatment with neuraminidase was shown to remove this si
alic acid, as well as most of the sialic acid present at the cell surf
ace. Applied to MCF-7/AZ, and MCF-7/6 cells, pretreatment with neurami
nidase abolished spontaneous as well as IGF-I induced, E-cadherin-depe
ndent fast cell-cell adhesion of cells in suspension, as measured in t
he fast aggregation assay. Treatment with neuraminidase did not, howev
er, inhibit the possibly different, but equally E-cadherin-mediated, p
rocess of cell-cell adhesion of MCF-7 cells on a flat plastic substrat
e as assessed by determining the percentage of cells remaining isolate
d (without contact with other cells) 24 h after plating.