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Ukr Biochem J ; 89(1): 38-49, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-29236388

RESUMO

We have studied the effect of hypoxia on the expression level of mRNA of the basic enzymes of pentose-phosphate cycle (G6PD, TKT, TALDO1, PGLS and RPIA) and glucose-6-phosphate isomerase (GPI) in U87 glioma cells in relation to inhibition of IRE1 (inositol requiring enzyme 1). It was shown that hypoxia leads to up-regulation of the expression of GPI and PGLS genes and to down-regulation of TALDO1 and RPIA genes in control glioma cells. Changes for GPI gene were more significant than for other genes. At the same time, inhibition of IRE1 modified the effect of hypoxia on the expression of all studied genes. In particular, it increased sensitivity to hypoxia of G6PD and TKT genes expression and suppressed the effect of hypoxia on the expression of GPI and RPIA genes. Additionally, inhibition of IRE1 eliminated hypoxic regulation of PGLS gene and did not change significantly effect of hypoxia on the expression of TALDO1 gene in glioma cells. Present study demonstrated that hypoxia, which often contributes to tumor growth, affects the expression of most studied genes and inhibition of IRE1 modified the hypoxic regulation of pentose-phosphate cycle gene expressions in a gene specific manner and thus possibly contributes to slower glioma growth, but several aspects of this regulation warrant further investigation.


Assuntos
Estresse do Retículo Endoplasmático/genética , Endorribonucleases/genética , Regulação Neoplásica da Expressão Gênica , Neuroglia/metabolismo , Via de Pentose Fosfato/genética , Proteínas Serina-Treonina Quinases/genética , Aldose-Cetose Isomerases/genética , Aldose-Cetose Isomerases/metabolismo , Hidrolases de Éster Carboxílico/genética , Hidrolases de Éster Carboxílico/metabolismo , Hipóxia Celular , Linhagem Celular Tumoral , Movimento Celular , Proliferação de Células , Endorribonucleases/deficiência , Técnicas de Silenciamento de Genes , Glucose-6-Fosfato Isomerase/genética , Glucose-6-Fosfato Isomerase/metabolismo , Glucosefosfato Desidrogenase/genética , Glucosefosfato Desidrogenase/metabolismo , Humanos , Neuroglia/patologia , Proteínas Serina-Treonina Quinases/deficiência , Transdução de Sinais , Transaldolase/genética , Transaldolase/metabolismo , Transcetolase/genética , Transcetolase/metabolismo
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