Quantification of VEGF isoforms and VEGFR transcripts by qRT-PCR and their significance in acute myeloid leukemia

Autor: Marie-Pierre Podgorniak, Géraldine Lescaille, Fabien Calvo, Raphaël Porcher, Philippe Rousselot, Hervé Dombret, Samia Mourah, Jacques Medioni, Benyoussef Naimi, Géraldine Labarchède
Rok vydání: 2009
Předmět:
0301 basic medicine
Adult
Male
Vascular Endothelial Growth Factor A
Cancer Research
medicine.medical_specialty
Myeloid
Angiogenesis
Clinical Biochemistry
Biology
Sensitivity and Specificity
Pathology and Forensic Medicine
03 medical and health sciences
chemistry.chemical_compound
Young Adult
0302 clinical medicine
Internal medicine
medicine
Biomarkers
Tumor

Humans
Protein Isoforms
RNA
Messenger

RNA
Neoplasm

Receptor
Aged
DNA Primers
Immunoassay
Vascular Endothelial Growth Factor Receptor-1
Base Sequence
Reverse Transcriptase Polymerase Chain Reaction
Myeloid leukemia
Middle Aged
medicine.disease
Prognosis
Vascular Endothelial Growth Factor Receptor-2
Vascular endothelial growth factor
Haematopoiesis
Leukemia
Leukemia
Myeloid
Acute

030104 developmental biology
medicine.anatomical_structure
Real-time polymerase chain reaction
Endocrinology
Oncology
chemistry
030220 oncology & carcinogenesis
Case-Control Studies
Cancer research
Female
Zdroj: The International journal of biological markers. 24(1)
ISSN: 0393-6155
Popis: Vascular endothelial growth factor (VEGF) and its receptors are known to play an important role in normal and pathological hematopoiesis but the prognostic impact of VEGF isoform transcripts in acute myeloid leukemia (AML) has not been addressed. We conducted a single-institution prospective study to analyze the impact of these angiogenic factors and the expression of their receptors on the survival of adult patients newly diagnosed with AML. We investigated the levels of VEGF transcript isoforms VEGF121, -145, -165, -189 and -206 and their receptors, VEGFR-1 and VEGFR-2, using quantitative reverse transcriptase polymerase chain reaction assays in peripheral blood mononuclear cells (PBMCs) of 67 consecutive AML patients at diagnosis. VEGF total protein was measured for comparison with mRNA levels in PBMCs. The VEGF121 splice variant transcript in AML PBMCs was significantly higher than in the normal controls. VEGF transcripts were quantified in all samples while its protein was detected in 42/67 (63%) of AML samples. High levels of VEGF121, VEGF165 transcripts and VEGF protein in AML were significantly related to a worse prognosis when analyzing overall survival (p121 expression remained an independent prognostic factor for either event-free survival or overall survival [aHR=8.83 (3.48–22.4), p121 mRNA in circulating cells from AML patients is a strong independent prognostic parameter, which could be useful in the management of unselected AML patients.
Databáze: OpenAIRE