Pregled bibliografske jedinice broj: 1260241
Gangliosides of human glioblastoma multiforme: a comprehensive mapping and structural analysis by ion mobility tandem mass spectrometry
Gangliosides of human glioblastoma multiforme: a comprehensive mapping and structural analysis by ion mobility tandem mass spectrometry // Journal of the American Society for Mass Spectrometry, 32 (2021), 5; 1249-1257 doi:10.1021/jasms.1c00088 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 1260241 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Gangliosides of human glioblastoma multiforme: a comprehensive mapping and structural analysis by ion mobility
tandem mass spectrometry
(Gangliosides of human glioblastoma multiforme: a comprehensive mapping and structural analysis by
ion mobility tandem mass spectrometry)
Autori
Sarbu, Mirela ; Petrica, Ligia ; Clemmer, David E. ; Vukelić, Željka ; Zamfir, Alina D.
Izvornik
Journal of the American Society for Mass Spectrometry (1044-0305) 32
(2021), 5;
1249-1257
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
human glioblastoma multiforme ; gangliosides ; biomarker ; ion mobility separation/spectrometry mass spectrometry (IMS MS) ; collision-induced dissociation
Sažetak
Glioblastoma multiforme (GBM), a malignant, highly aggressive, grade IV brain tumor, which rapidly infiltrates into the nearby tissue, has drawn a significant amount of attention because of its poor prognosis and the limited treatment options available. In GBM, nearly all tumor cells exhibit aberrant cell-surface glycosylation patterns due to the alteration of their biosynthesis or postsynthesis modification process. Since gangliosides (GGs) are acknowledged as tumor- associated antigens, we have carried out here a comprehensive profiling of native ganglioside mixtures extracted and purified from GBM specimens. For this purpose, high performance ion mobility separation mass spectrometry (IMS MS) was thoroughly optimized to allow the discovery of GBM-specific structures and the assessment of their roles as tumor markers or possible associated antigens. GG separation by IMS according to the charge state, carbohydrate chain length, degree of sialylation, and ceramide composition led to the identification of no less than 160 distinct components, which represents 3- fold the number of structures identified before. The detected GGs and asialo-GGs were found characterized by a high heterogeneity in their ceramide and glycan compositions, encompassing up five Neu5Ac residues. The tumor was found dominated in equal and high proportions by GD3 and GT1 forms, with a particular incidence of C24:1 fatty acids in the ceramide. By the occurrence of only one mobility feature and the diagnostic fragment ions, the IMS tandem MS conducted using collision-induced dissociation (CID) disclosed for the first time the presence of GT1c(d18:1/24:1) newly proposed here as a potential GBM marker.
Izvorni jezik
Engleski
Znanstvena područja
Kemija, Interdisciplinarne prirodne znanosti, Temeljne medicinske znanosti
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE