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Bone marrowVEGFCexpression is associated with multilineage dysplasia and several prognostic markers in adult acute myeloid leukemia, but not with survival

Authors :
Llorenç Font
Maria Luz Amigo
Carme Pedro
Ana Garrido
David Gallardo
Antoni Garcia-Guiñon
Maria Paz Queipo De Llano
Josep-Maria Ribera
Josep M Marti-Tutusaus
Salut Brunet
Lourdes Escoda
Olga Salamero
Marisa Calabuig
Montserrat Arnan
Vicent Guillem
Carme Talarn
Jordi Sierra
Montserrat Hoyos
Jordi Esteve
Josep F. Nomdedeu
Joan Bargay
Mar Tormo
Blanca Navarro
Marina Díaz-Beyá
Antonia Sampol
Source :
LEUKEMIA & LYMPHOMA, r-IGTP. Repositorio Institucional de Producción Científica del Instituto de Investigación Germans Trias i Pujol, instname, r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau, r-INCLIVA. Repositorio Institucional de Producción Científica de INCLIVA
Publication Year :
2018
Publisher :
Informa UK Limited, 2018.

Abstract

Vascular endothelial growth factor C (VEGFC) stimulates leukemia cell proliferation and survival, and promotes angiogenesis. We studied VEGFC expression in bone marrow samples from 353 adult acute myeloid leukemia (AML) patients and its relationship with several clinical, cytogenetic, and molecular variables. We also studied the expression of 84 genes involved in VEGF signaling in 24 patients. We found that VEGFC expression was higher in AML patients with myelodysplasia-related changes (AML-MRC) than in patients with non-AML-MRC. We also found an association between VEGFC expression and the patient cytogenetic risk group, with those with a worse prognosis having higher VEGFC expression levels. No correlation was observed between VEGFC expression and survival or complete remission. VEGFC expression strongly correlated with expression of the VEGF receptors FLT1, KDR, and NRP1. Thus, in this series, VEGFC expression was increased in AML-MRC and in subgroups with a poorer prognosis, but has no impact on survival.

Details

ISSN :
10292403 and 10428194
Volume :
59
Database :
OpenAIRE
Journal :
Leukemia & Lymphoma
Accession number :
edsair.doi.dedup.....5af314581e9ca7b58e24ac0d36841059
Full Text :
https://doi.org/10.1080/10428194.2017.1422858