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[Behavior of glucosephosphate isomerase in children with malignant diseases]
Insights
Glucose-phosphate-isomerase (GPI) levels vary in children and are elevated in various conditions, not just tumors. Elevated GPI in osteogenic sarcoma or medulloblastoma correlates with tumor stage, but it is not a reliable tumor marker for all cancers.
Area of Science:
- Biochemistry and Clinical Enzymology
- Pediatric Oncology Biomarkers
Context:
- Glucose-phosphate-isomerase (GPI) is an enzyme found in plasma.
- Normal GPI ranges differ significantly across pediatric age groups.
- Elevated GPI has been observed in various pediatric conditions.
Purpose:
- To evaluate the diagnostic utility of plasma glucose-phosphate-isomerase (GPI) activity as a tumor marker in children.
- To correlate GPI activity with clinical tumor stage in specific pediatric malignancies.
- To assess the reliability of GPI as a general tumor marker across different pediatric cancers and non-malignant conditions.
Summary:
- Plasma GPI levels exhibit age-dependent variations in children, with established normal ranges.
- While GPI activity correlates with tumor stage in osteogenic sarcoma and medulloblastoma, its sensitivity is low in Ewing sarcoma and myeloid leukemia.
- High GPI activity is also observed in non-malignant conditions like cystic fibrosis, diabetes mellitus, and muscular dystrophy, limiting its specificity.
Impact:
- Plasma GPI is not a universally valid tumor marker for pediatric cancers due to inconsistent correlation and elevation in non-malignant diseases.
- Routine measurement of GPI activity is not recommended as part of standard enzyme chemistry in pediatric diagnostics.
- This study clarifies the limited role of GPI in pediatric oncology, guiding diagnostic strategies and resource allocation.
Abstract:
The normal range of glucose-phosphate-isomerase (GPI) in the plasma of children during the first month of life is up to 80 U/l; until the end of the second year of life between 11 and 50 U/l; thereafter the upper limit is 46 U/l. In osteogenic sarcoma or medulloblastoma there is a good correlation between activity of GPI in plasma and clinical tumor stage. In a lot of other tumors sensitivity of this enzyme is either very low as in Ewing-sarcoma or myeloic leukemia or there is no consistent relation to the extent of the tumor. High activities of GPI are equally obtained in children suffering from cystic fibrosis, diabetes mellitus or muscular dystrophy. GPI is not valid as a tumor marker even being raised in sarcoma and medulloblastoma as mentioned. So it is not necessary to check GPI activity as a part of routine enzyme chemistry.
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