Glycolipid markers of astrocytomas and oligodendrogliomas

Citation
Aj. Yates et al., Glycolipid markers of astrocytomas and oligodendrogliomas, J NE EXP NE, 58(12), 1999, pp. 1250-1262
Citations number
70
Categorie Soggetti
Neurosciences & Behavoir
Journal title
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY
ISSN journal
00223069 → ACNP
Volume
58
Issue
12
Year of publication
1999
Pages
1250 - 1262
Database
ISI
SICI code
0022-3069(199912)58:12<1250:GMOAAO>2.0.ZU;2-D
Abstract
Neutral glycolipids and gangliosides were analyzed in 149 astrocytomas (A), 46 oligodendrogliomas (O), and 21 oligoastrocytomas (OA) to determine if s pecific glycolipids correlate with histologic diagnosis and grade. Positivi ty for asialoGM1 (GA1) and negativity for paragloboside by immuno-TLC corre lated with histological diagnosis of O and OA, whereas the reverse pattern correlated with A. High levels (over 5 mu g hexose per mg dry weight) of CM H generally correlated with an O component, but the association was not as strong as for either GA1 presence or paragloboside absence. Pilocytic astro cytomas and pleomorphic xanthoastrocytomas had high proportions (> 15%) of globoside, low ratios (< 0.5) of GD1a: GD1b, and identifiable ceramide trih exoside (CTH). Three gangliosides of the Ib pathway were progressively lost with increasing grade of A, but a similar correlation with grade was not s een in O or OA. A high proportion of cases expressing sialosylparagloboside (3'LM1; 6'LM1) were grade 4 A. Glycolipids are synthesized by glycosyltran sferases that add specific sugars to the nascent oligosaccharide. Correlati on of specific glycolipids with histological diagnoses and grades indicate that these tumor types express specific patterns of glycosyltransferases, s everal of which have been cloned. It is possible that critical genes coding for these enzymes are deleted, overexpressed, or mutated in certain tumor types and grades, thus leading to the patterns of glycolipids that we found to be associated with these tumors.