
Expression of proliferation related transcription factor genes in U87 ...
Inhibition of ERN1/IRE1 (endoplasmic reticulum to nucleus signaling 1/inositol requiring enzyme 1), a central mediator of endoplasmic reticulum stress, significantly suppresses glioma cell proliferation and tumor growth as well as modifies sensitivity gene expressions to glucose and glutamine deprivation.
A novel IRE1 kinase inhibitor for adjuvant glioblastoma treatment
Inositol-requiring enzyme 1 (IRE1) is a major mediator of the unfolded protein response (UPR), which is activated upon endoplasmic reticulum (ER) stress. Tumor cells experience ER stress due to adverse microenvironmental cues, a stress overcome by relying on IRE1 signaling as an adaptive mechanism.
High epiregulin expression in human U87 glioma cells relies on …
2013年12月13日 · Inhibition of IRE1α dramatically reduced EREG expression both in cell culture and in human xenograft tumor models. The high-expression rate of EREG in U87 cells was therefore linked to IRE1α, although being modestly affected by chemical inducers of the endoplasmic reticulum stress.
Expression of IDE and PITRM1 genes in ERN1 knockdown U87 ... - PubMed
2020年7月1日 · Objective: The aim of the present investigation was to study the expression of genes encoding polyfunctional proteins insulinase (insulin degrading enzyme, IDE) and pitrilysin metallopeptidase 1 (PITRM1) in U87 glioma cells in response to inhibition of endoplasmic reticulum stress signaling mediated by ERN1/IRE1 (endoplasmic reticulum to ...
High epiregulin expression in human U87 glioma cells relies on …
IRE1α is a transmembrane protein of the endoplasmic reticulum (ER) and an upstream activator of the JNK to EGFR signaling ①. IRE1 kinase, but not the IRE1 RNase domain, contributes to the high level of EREG production in these cells.
(PDF) High epiregulin expression in human U87 glioma
2013年12月13日 · Inhibition of IRE1alpha dramatically reduced EREG expression both in cell culture and in human xenograft tumor models. The high-expression rate of EREG in U87 cells was therefore linked to...
Local intracerebral inhibition of IRE1 by MKC8866 sensitizes ...
2020年12月1日 · A principal component analysis revealed that GL261 co-clustered with U87, overexpressing the wild type IRE1 or the P336L mutant (in which IRE1 is constitutively activated), treated or not with tunicamycin, thereby indicating that the IRE1 pathway might be constitutively activated in GL261 cells as previously observed in other cell lines [8].
A novel IRE1 kinase inhibitor for adjuvant glioblastoma treatment
2023年5月19日 · Inositol-requiring enzyme 1 (IRE1) is a major mediator of the unfolded protein response (UPR), which is activated upon endoplasmic reticulum (ER) stress. Tumor cells experience ER stress due to adverse microenvironmental cues, a stress overcome by relying on IRE1 signaling as an adaptive mechanism.
Expression of tumor growth related genes in IRE1 knockdown U87 …
We have studied the effect of IRE1 signaling enzyme knockdown as well as hypoxia on the expression of genes encoding the important tumor growth related proteins (BRCA1, DEK, BCL2L1, COL6A1, TPD52, HOMER3, and GNPDA1) in U87 glioma cells.
INHIBITION OF IRE1 MODIFIES EFFECT OF GLUCOSE DEPRIVATION ON ... - PubMed
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 gl …