Glycosphingolipids in human abdominal leiomyosarcoma and liposarcoma

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Authors: Chunsheng Jin, Anders Thornell, Marta Berndsen, Karin Säljö, Eva Jennische, Susann Teneberg
Cited by: 0
References: 57

Abstract

Retroperitoneal sarcomas (liposarcomas and leiomyosarcomas) are rare and highly malignant mesenchymal tumors with poor prognosis, since they often reach a large size before detection, due to their anatomical location. Thus, development of new tumor biomarkers for early detection of these cancers is urgently needed. In search for potential sarcoma biomarkers this study examined the glycosphingolipid profiles of one leiomyosarcoma and one liposarcoma by mass spectrometry, enzymatic hydrolysis and by binding of carbohydrate recognizing ligands. Detailed mass spectrometry analyses of oligosaccharides released from the glycosphingolipids showed that the liposarcoma had a number of glycosphingolipids previously found in many human tissues (the gangliosides GM3, GD3, GM2, GD1a, sialylneolactotetra- and hexaosylceramide, and globo- and lactotriaosylceramide, globo- and lactotetraosylceramide, x 2 pentaosylceramide, H type 2 penta- and heptaosylceramide, neolactotetra- and heptaosylceramide). The leiomyosarcoma had a more complex glycosphingolipid composition, and, in addition to the compounds listed above, it contained sialyl-lactotetraosylceramide, sialyl-globotetraosylceramide, globopentaosylceramide/SSEA-3, sialyl-globopentaosylceramide/SSEA-4 and disialyl-globopentaosylceramide in this tumor. The expression of sialyl-globopentaosylceramide/SSEA-4 in leiomyosarcoma was confirmed by immunohistochemistry. Thus, the leiomyosarcoma had several glycosphingolipids also found in human pluripotent stem cells. These insights may have important clinical implications for the development of novel diagnostic and therapeutic strategies for sarcomas.

Fields of Study & Subjects

Glycosylation and Glycoproteins Research Sarcoma Diagnosis and Treatment Sphingolipid Metabolism and Signaling

Publication details

Journal / source
Journal of Biological Chemistry
Volume
302
Issue
4
Pages
111327–111327
Publication date
26 February 2026
Language
EN