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Updated: Jun 7, 2026

A Simple Bioassay for the Evaluation of Vascular Endothelial Growth Factors
Published on: March 15, 2016
Vascular Endothelial Growth Factor A isoform mRNA expression in pediatric acute myeloid leukemia
R C Kruizinga1, H J M de Jonge, K R Kampen
1Division of Pediatric Oncology/Hematology, Department of Pediatrics, Beatrix Children's Hospital, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.
Abstract:
In AML high VEGFA protein expression correlates with poor overall and relapse-free survival (OS/RFS). To date, the relevance of the various VEGFA isoforms is unclear. We determined VEGF121, VEGF145, VEGF148, VEGF165, VEGF183, and VEGF189 mRNA expression in pediatric AML samples and investigated the relation between VEGFA isoform expression and clinicopatholologic characteristics and outcome. A significant co-expression of VEGF121, VEGF165, VEGF183, and VEGF189 isoforms was apparent (mean rho = 0.716, P < 0.0001). This co-expression justifies measuring a single VEGFA isoform (e.g., 121, 165, 183, and 189) as representative expression of all VEGFA isoforms in future studies designed to determine the prognostic importance of VEGFA isoforms.
Insights
High vascular endothelial growth factor A (VEGFA) protein expression in acute myeloid leukemia (AML) predicts poor survival. Specific VEGFA isoforms (VEGF121, VEGF165, VEGF183, VEGF189) show significant co-expression, suggesting one can represent all in future prognostic studies.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- High vascular endothelial growth factor A (VEGFA) protein expression is linked to poor overall survival (OS) and relapse-free survival (RFS) in acute myeloid leukemia (AML).
- The prognostic significance of individual VEGFA isoforms in AML remains largely undetermined.
Purpose of the Study:
- To investigate the mRNA expression levels of various VEGFA isoforms in pediatric AML.
- To explore the correlation between VEGFA isoform expression and clinicopathologic features and patient outcomes.
Main Methods:
- Quantification of VEGF121, VEGF145, VEGF148, VEGF165, VEGF183, and VEGF189 mRNA expression in pediatric AML patient samples.
- Statistical analysis to assess co-expression patterns and relationships with clinical characteristics and survival data.
Main Results:
- A significant co-expression was observed among VEGF121, VEGF165, VEGF183, and VEGF189 isoforms (mean rho = 0.716, P < 0.0001).
- These findings suggest a coordinated expression pattern for a subset of VEGFA isoforms.
Conclusions:
- The co-expression of specific VEGFA isoforms (VEGF121, VEGF165, VEGF183, VEGF189) in pediatric AML supports using a single representative isoform for future prognostic studies.
- Measuring one of these isoforms could serve as a surrogate for overall VEGFA isoform expression in assessing prognostic importance in AML.
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