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Cellular roles of ganglioside GM3 biosynthesis in human cancer ce | 4044
Journal of Glycobiology

Journal of Glycobiology
Open Access

ISSN: 2168-958X

+44 1478 350008

Cellular roles of ganglioside GM3 biosynthesis in human cancer cells


Glycobiology World Congress

August 10-12, 2015 Philadelphia, USA

Cheorl-Ho Kim

Scientific Tracks Abstracts: J Glycobiol

Abstract :

Ganglioside GM3, sialic acid (NeuAc)-containing glycosphingolipid is the first and the simplest of the gangliosides and are
found on the outer leaflet of the plasma membrane in vertebrates. It plays important roles in a large variety of biological
processes such as cellular interactions, differentiation, oncogenesis, adhesion, cell growth and receptor function in various cell
systems. Ganglioside GM3 is synthesized by lactosylceramide α-2, 3-sialyltransferase (hST3Gal V, EC 2.4.99.9) which catalyzes
the transfer of NeuAc from CMP-NeuAc to the non-reducing terminal galactose of lactosylceramide in human. The amount of
ganglioside GM3 increases with a concomitant increase of hST3Gal V activity during megakaryocytic differentiation of K562
cells treated with PMA that is a megakaryocytic differentiation inducer but not with an erythrocyte differentiation inducer,
hemin. Ganglioside GM3 may play an important role as a trigger in differentiation induction of K562 cells. The hST3Gal V
is a key regulatory enzyme for ganglioside biosynthesis because it catalyzes the first committed step in the synthesis of nearly
all gangliosides. Differentiation of K562 cells requires Erk1/2 activation and p38 MAPK inhibition for the transcriptional
activity of lactosylceramide α-2, 3-sialyltransferase (hST3Gal V) and synthesis of ganglioside GM3. The expression of hST3Gal
V mRNA induces expression of the megakaryocytic markers and differentiation of K562 cells. Ganglioside GM3 mediates
megakaryocytic differentiation of human chronic myelogenous cells and apoptosis of many human cancer cells.

Biography :

Cheorl-Ho Kim has completed his PhD at the age of 28 years from The University of Tokyo and was positioned as a Senior Scientist from Korea Research Institute of
Bioscience and Biotechnology. He is a Professor of Molecular Glycobiology, Sung Kyun Kwan University, Korea, leading organization of Korea which is cooperated
with the SamSung Group. He has published more than 337 papers in reputed journals and serving as an Editorial Board Member, Executive Editor and Editor-
In Chief of the international journals. His work was contributed to the mechanisms of glycan-mediated Hepatitis B viral oncogenesis and invasion, sialoglycanmediated
leukemic differentiation and vascular biology. He is being serves as an Editor-in-Chief of Journal of Glycobiology, Editor-in-Chief of Journal of Microbial and
Biochemical Technology, Executive Editor of Journal of Glycomics and Lipidomics and Editor of eCAM.

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