Suppression of a sialyltransferase by antisense DNA reduces invasiveness of human colon cancer cells in vitro

Transfer of terminal alpha2,6-linked sialic acids to N-glycans is catalyzed by beta -galactoside alpha2,6-sialyltransferase (ST6Gal I). Expression of STGGal I and its products is reportedly increased in colon cancers. To investigate directly the functional effects of ST6Gal I expression, human colon cancer (HT29) cells were transfected with specific antisense DNA. ST6Gal I mRNA and protein were virtually undetectable in six strains of transfected HT29 cells. STGGal activity was reduced to 14% of control (P<0.005) in transfected cells. Expression of terminal 2,6- and alpha2,3-linked sialic acids, and unmasked N-acetyllactosamine oligosaccharides, respectively, was assessed using flow cytometry and fluoresceinated Sambucus nigra, Maackia amurensis and Erythrina cristagalli lectins. Results indicated a major reduction in expression of alpha2,6-linked sialic acids and counterbalancing increase in unmasked N-acetyllactosamines in antisense DNA-transfected cells, without altered expression of alpha2,3-linked sialic acids or ganglioside profiles. The ability of transfected cells to form colonies in soft agar and to invade extracellular matrix material (Matrigel), respectively, in vitro was reduced by approx. 98% (P < 0.0001) and more than 3-fold (P < 0.005) compared to parental HT29 cells. These results indicate that N-glycans bearing terminal alpha2,6-linked sialic acids may enhance the invasive potential of colon cancer cells. (C) 2001 Elsevier Science B.V. All rights reserved.