INHIBITION OF IRE1 MODIFIES EFFECT OF GLUCOSE DEPRIVATION ON THE EXPRESSION OF TNFα-RELATED GENES IN U87 GLIOMA CELLS
| Autor: | N A Hlushchak, Dmytro O. Minchenko, Oleksandr H. Minchenko, O O Ratushna, L L Karbovskyi, I V Kryvdiuk |
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| Předmět: |
Endoribonuclease activity
TNFRSF1A LITAF Biochemistry Receptors Tumor Necrosis Factor lcsh:QD415-436 TNFAIP1 TNFAIP3 Regulation of gene expression Chemistry glucose deprivation TNFRSF21/DR6 Intracellular Signaling Peptides and Proteins Nuclear Proteins Endoplasmic Reticulum Stress TNF Receptor-Associated Death Domain Protein Cell biology DNA-Binding Proteins Gene Expression Regulation Neoplastic Receptors Tumor Necrosis Factor Type I Tumor necrosis factor alpha Signal transduction Neuroglia IRE1 inhibition Signal Transduction Protein Serine-Threonine Kinases lcsh:Biochemistry Glioma Cell Line Tumor Endoribonucleases medicine TNFRSF11B Humans TNFRSF10B/DR5 RNA Messenger Tumor Necrosis Factor alpha-Induced Protein 3 Adaptor Proteins Signal Transducing Cell Proliferation Cell growth Tumor Necrosis Factor-alpha Osteoprotegerin mRNA expression Proteins medicine.disease TRADD Receptors TNF-Related Apoptosis-Inducing Ligand Tumor Necrosis Factor Decoy Receptors Glucose Cell culture glioma cells TNFRSF10D CD27 Ligand Transcription Factors |
| Zdroj: | Europe PubMed Central Ukrainian Biochemical Journal, Vol 87, Iss 6, Pp 36-51 (2015) |
| Popis: | Inhibition of IRE1 (inositol requiring enzyme-1), the major signaling pathway of endoplasmic reticulm stress, significantly decreases glioma cell proliferation and tumor growth. We have studied the expression of TNFα-related genes and effect of glucose deprivation on these gene expressions in U87 glioma cells over-expressing dominant-negative IRE1 defective in both kinase and endonuclease (dn-IRE1) activity of IRE1 with hopes of elucidating its contribution to IRE1 mediated glioma growth. We have demonstrated that glucose deprivation condition leads to down-regulation of the expression of TNFRSF11B, TNFRSF1A, TNFRSF10D/TRAILR4, and LITAF genes and up-regulation of TNFRSF10B/TRAILR2/DR5 gene at the mRNA level in control glioma cells. At the same time, the expression of TNFRSF21/DR6, TNFAIP1, TNFAIP3, TRADD, and CD70/TNFSF7 genes in control glioma cells is resistant to glucose deprivation condition. The inhibition of IRE1 modifies the effect of glucose deprivation on LITAF, TNFRSF21, TNFRSF11B, and TRADD gene expressions and induces sensitivity to glucose deprivation condition the expression of TNFRSF10B, TNFRSF1A, and CD70 genes. We have also demonstrated that the expression of all studied genes is affected in glioma cells by inhibition of IRE1, except TNFRSF1A gene, as compared to control glioma cells. Moreover, the changes in the expression of TNFRSF1A, TNFRSF10D/TRAILR4, and LITAF genes induced by glucose deprivation condition have opposite orientation to that induced by inhibition of IRE1. The present study demonstrates that fine-tuning of the expression of TNFα-induced proteins and TNF receptor superfamily genes, which related to cell death and proliferation, is regulated by IRE1, an effector of endoplasmic reticulum stress, as well as depends on glucose deprivation in gene specific manner. Thus, the inhibition of kinase and endoribonuclease activity of IRE1 correlates with deregulation of TNFα-induced protein genes and TNF receptor superfamily genes in gene specific manner and thus slower the tumor growth. |
| Databáze: | OpenAIRE |
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