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VEGFC Antibody Therapy Drives Differentiation of AML.
Kampen, Kim R; Scherpen, Frank J G; Mahmud, Hasan; Ter Elst, Arja; Mulder, André B; Guryev, Victor; Verhagen, Han J M P; De Keersmaecker, Kim; Smit, Linda; Kornblau, Steven M; De Bont, Eveline S J M.
Afiliação
  • Kampen KR; Division of Pediatric Oncology/Hematology, Department of Pediatrics, Beatrix Children's Hospital, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands. kim.kampen@kuleuven.be edebont@elkerliek.nl.
  • Scherpen FJG; Laboratory for Disease Mechanisms in Cancer, Department of Oncology, KU Leuven, University of Leuven, Leuven Cancer Institute (LKI), Leuven, Belgium.
  • Mahmud H; Division of Pediatric Oncology/Hematology, Department of Pediatrics, Beatrix Children's Hospital, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.
  • Ter Elst A; Division of Pediatric Oncology/Hematology, Department of Pediatrics, Beatrix Children's Hospital, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.
  • Mulder AB; Division of Pediatric Oncology/Hematology, Department of Pediatrics, Beatrix Children's Hospital, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.
  • Guryev V; Department of Laboratory Medicine, University Medical Center Groningen, Groningen, the Netherlands.
  • Verhagen HJMP; European Research Institute for the Biology of Ageing, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.
  • De Keersmaecker K; Department of Hematology, VU University Medical Center, Cancer Center Amsterdam, Amsterdam, the Netherlands.
  • Smit L; Laboratory for Disease Mechanisms in Cancer, Department of Oncology, KU Leuven, University of Leuven, Leuven Cancer Institute (LKI), Leuven, Belgium.
  • Kornblau SM; Department of Hematology, VU University Medical Center, Cancer Center Amsterdam, Amsterdam, the Netherlands.
  • De Bont ESJM; Department of Leukemia, The University of Texas M.D. Anderson Cancer, Houston, Texas.
Cancer Res ; 78(20): 5940-5948, 2018 10 15.
Article em En | MEDLINE | ID: mdl-30185550
High expression of VEGFC predicts adverse prognosis in acute myeloid leukemia (AML). We therefore explored VEGFC-targeting efficacy as an AML therapy using a VEGFC mAb. VEGFC antibody therapy enforced myelocytic differentiation of clonal CD34+ AML blasts. Treatment of CD34+ AML blasts with the antibody reduced expansion potential by 30% to 50% and enhanced differentiation via FOXO3A suppression and inhibition of MAPK/ERK proliferative signals. VEGFC antibody therapy also accelerated leukemia cell differentiation in a systemic humanized AML mouse model. Collectively, these results define a regulatory function of VEGFC in CD34+ AML cell fate decisions via FOXO3A and serve as a new potential differentiation therapy for patients with AML.Significance: These findings reveal VEGFC targeting as a promising new differentiation therapy in AML. Cancer Res; 78(20); 5940-8. ©2018 AACR.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Leucemia Mieloide Aguda / Fator C de Crescimento do Endotélio Vascular / Anticorpos Monoclonais Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Revista: Cancer Res Ano de publicação: 2018 Tipo de documento: Article País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Leucemia Mieloide Aguda / Fator C de Crescimento do Endotélio Vascular / Anticorpos Monoclonais Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Revista: Cancer Res Ano de publicação: 2018 Tipo de documento: Article País de publicação: Estados Unidos