Phospholipase D activates HIF-1-VEGF pathway via phosphatidic acid
Experimental & Molecular Medicine
; : e126-2014.
Article
em En
| WPRIM
| ID: wpr-113787
Biblioteca responsável:
WPRO
ABSTRACT
Growth factor-stimulated phospholipase D (PLD) catalyzes the hydrolysis of phosphatidylcholine (PC), generating phosphatidic acid (PA) which may act as a second messenger during cell proliferation and survival. Therefore, PLD is believed to play an important role in tumorigenesis. In this study, a potential mechanism for PLD-mediated tumorigenesis was explored. Ectopic expression of PLD1 or PLD2 in human glioma U87 cells increased the expression of hypoxia-inducible factor-1alpha (HIF-1alpha) protein. PLD-induced HIF-1 activation led to the secretion of vascular endothelial growth factor (VEGF), a HIF-1 target gene involved in tumorigenesis. PLD induction of HIF-1alpha was significantly attenuated by 1-butanol which blocks PA production by PLD, and PA per se was able to elevate HIF-1alpha protein level. Inhibition of mTOR, a PA-responsive kinase, reduced the levels of HIF-1alpha and VEGF in PLD-overexpressed cells. Epidermal growth factor activated PLD and increased the levels of HIF-1alpha and VEGF in U87 cells. A specific PLD inhibitor abolished expression of HIF-1alpha and secretion of VEGF. PLD may utilize HIF-1-VEGF pathway for PLD-mediated tumor cell proliferation and survival.
Texto completo:
1
Base de dados:
WPRIM
Assunto principal:
Ácidos Fosfatídicos
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Fosfolipase D
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Transfecção
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Transdução de Sinais
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Regulação Neoplásica da Expressão Gênica
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Linhagem Celular Tumoral
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Fator A de Crescimento do Endotélio Vascular
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Fator de Crescimento Epidérmico
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Subunidade alfa do Fator 1 Induzível por Hipóxia
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Glioma
Limite:
Humans
Idioma:
En
Revista:
Experimental & Molecular Medicine
Ano de publicação:
2014
Tipo de documento:
Article