The banding patterns of chromosomes from 20 patients with chronic lymphocytic leukaemia (C.L.L.) have been analyzed. 97 of 100 metaphases examined had a normal banding pattern. The 3 remaining metaphases, all from one patient had bands similar to those seen after aging. It is concluded that the chro
Gangliosides in human chronic lymphocytic leukaemia
✍ Scribed by Nguyen Anh-Tuan; Judit Pick; János Vajda; Veronika Harsányi; Susan R. Hollán
- Publisher
- John Wiley and Sons
- Year
- 1985
- Tongue
- French
- Weight
- 410 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0020-7136
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✦ Synopsis
Gangliosides were analysed by elaborated overpressured thin-layer chromatography (OPTLC) in 6 cell samples from 5 patients with chronic lymphocytic leukaemia (CLL) of Btell origin, and 4 individual lymphocyte preparations from normal blood donors. The principal difference in the ganglioside profile between these two counterparts appears to be the presence of GD3 and the predominance of the less polar compounds (GM3, GM2, GMI) in CLL cells. Qualitatively, GD, accounted for about 5.5% of the total CLL gangliosides, whereas it was not detectable in normal lymphocytes. Quantitatively, GM3 constituted more than 81 % of the total CLL gangliosides. a proportion more than twice as high as that found in normal lymphocytes. Three other minor gangliosides were isolated from CLL cells; these were shown to be GM2 (trace amounts), GMI (7.7%), and GDI (4%). The expression of individual gangliosides varied greatly among the various CLL samples obtained from different patients, and even from the same patient, if examined at different times. No gangliosides were found in the supernatant collected from CLL cells subjected to a temperature shift (OOC to 37OC) or in the cell-free medium harvested from the CLL cells kept in overnight culture. 'To whom reprint requests should be sent, at the N.I.H.B.T., Budapest XI. Daroczi u. 24, H-1502 Hungary. ''y'J''
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Sequential cytogenetic studies were performed on a minimum of two and a maximum of nine occasions (mean 3.6) on the peripheral blood leucocytes of 112 patients with B-CLL. On initial cytogenetic analysis, 58 had a normal karyotype and 64 had a clonal abnormality. Karyotypic evolution occurred in 18
## Abstract B‐cell chronic lymphocytic leukaemia (B‐CLL) is a heterogeneous disease with some patients having an indolent course never needs treatment, while others having rapidly progressive one requires intensive treatment. In recent decades, numerous prognostic markers, such as immunoglobulin va