1988
DOI: 10.1111/j.1365-2141.1988.tb02429.x
|View full text |Cite
|
Sign up to set email alerts
|

Plasma levels of highly sulphated glycosaminoglycans are raised in patients with chronic myeloid leukaemia

Abstract: A study of absolute basophil counts and plasma levels of highly sulphated glycosaminoglycans in 30 peripheral blood samples from 21 patients with different leukaemias was performed. This revealed significantly raised levels of both plasma highly sulphated glycosaminoglycans and basophils in those patients with chronic myeloid leukaemia, as compared to those with other types of leukaemia and 35 normal controls. A strong correlation (r = 0.83) was observed between the levels of highly sulphated glycosaminoglycan… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2

Citation Types

1
1
0

Year Published

1989
1989
2017
2017

Publication Types

Select...
5

Relationship

0
5

Authors

Journals

citations
Cited by 5 publications
(2 citation statements)
references
References 11 publications
1
1
0
Order By: Relevance
“…This agrees with the findings of Hasselbach et al [30]. Moreover, HA synthesis and release from the neoplastic clone cannot be excluded, since plasma levels of highly sulfated glycosaminoglycans are raised in patients with CML [43]. Serum HA could thus be considered as a potential prognostic marker in patients before treatment.…”
Section: Discussionsupporting
confidence: 80%
“…This agrees with the findings of Hasselbach et al [30]. Moreover, HA synthesis and release from the neoplastic clone cannot be excluded, since plasma levels of highly sulfated glycosaminoglycans are raised in patients with CML [43]. Serum HA could thus be considered as a potential prognostic marker in patients before treatment.…”
Section: Discussionsupporting
confidence: 80%
“…Further studies are necessary to determine a cut-off value that is diagnostic for HCC. Serum level of GAGs may increase in other diseases including rheumatoid arthritis (Friman et al, 1977), systemic lupus erythmatosus (Friman et al, 1987), chronic myeloid leukemia (Craig et al, 1988), and chronic lymphocytic leukemia, and in essential thrombocythaemia (Calabrò et al, 1998), limiting its specificity to liver diseases. Therefore, the combined measurement of serum level of GAGs and IGF-1 level may provide a more specific marker for liver diseases.…”
Section: Discussionmentioning
confidence: 99%