Source:http://linkedlifedata.com/resource/pubmed/id/21800645
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rdf:type | |
lifeskim:mentions |
umls-concept:C0007600,
umls-concept:C0014442,
umls-concept:C0017262,
umls-concept:C0017638,
umls-concept:C0017725,
umls-concept:C0017797,
umls-concept:C0037083,
umls-concept:C0079183,
umls-concept:C0185117,
umls-concept:C0441655,
umls-concept:C0871712,
umls-concept:C1280500,
umls-concept:C1333181,
umls-concept:C1710082,
umls-concept:C1822997,
umls-concept:C2911684
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pubmed:issue |
1
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pubmed:dateCreated |
2011-8-1
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pubmed:abstractText |
Ischemia has been shown to induce a set of complex intracellular signaling events known as the unfolded protein response, which is mediated by endoplasmic reticulum-nuclei-1 sensing enzyme. We have studied the expression of several cyclin and cyclin-dependent kinase genes which participate in the control of cell cycle and proliferation under ischemic conditions (glucose or glutamine deprivation) in endoplasmic reticulum-nuclei-1-deficient glioma cells. It was shown that blockade of endoplasmic reticulum-nuclei signaling enzyme-1, the key endoplasmic reticulum stress sensor, leads to an increase of the expression levels of cyclin-dependent kinase-2 and cyclin A2, D3, E2 and G2 genes but suppresses cyclin D1. Moreover, the expression level of cyclin-dependent kinase-2 as well as cyclin A2, D3 and E2 mRNAs is significantly decreased under glucose or glutamine deprivation conditions both in control and endoplasmic reticulum-nuclei-1-deficient glioma cells. However, cyclin-dependent kinase-4 and -5 mRNA expressions is increased, but in glucose deprivation conditions only. Results of this study have shown that the expression of most tested genes of encoded cyclins and cyclin-dependent kinases is dependent on endoplasmic reticulum-nuclei-1 signaling enzyme function both in normal and glutamine and glucose deprivation conditions and possibly participates in cell adaptive response to endoplasmic reticulum stress associated with ischemia.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Culture Media,
http://linkedlifedata.com/resource/pubmed/chemical/Cyclin-Dependent Kinases,
http://linkedlifedata.com/resource/pubmed/chemical/Cyclins,
http://linkedlifedata.com/resource/pubmed/chemical/ERN1 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Endoribonucleases,
http://linkedlifedata.com/resource/pubmed/chemical/Glucose,
http://linkedlifedata.com/resource/pubmed/chemical/Glutamine,
http://linkedlifedata.com/resource/pubmed/chemical/Protein-Serine-Threonine Kinases
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pubmed:status |
MEDLINE
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pubmed:issn |
0201-8470
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
83
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
18-29
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pubmed:meshHeading |
pubmed-meshheading:21800645-Cell Culture Techniques,
pubmed-meshheading:21800645-Cell Line, Tumor,
pubmed-meshheading:21800645-Cloning, Molecular,
pubmed-meshheading:21800645-Culture Media,
pubmed-meshheading:21800645-Cyclin-Dependent Kinases,
pubmed-meshheading:21800645-Cyclins,
pubmed-meshheading:21800645-Endoplasmic Reticulum,
pubmed-meshheading:21800645-Endoribonucleases,
pubmed-meshheading:21800645-Glioma,
pubmed-meshheading:21800645-Glucose,
pubmed-meshheading:21800645-Glutamine,
pubmed-meshheading:21800645-Humans,
pubmed-meshheading:21800645-Ischemia,
pubmed-meshheading:21800645-Protein Unfolding,
pubmed-meshheading:21800645-Protein-Serine-Threonine Kinases,
pubmed-meshheading:21800645-Reverse Transcriptase Polymerase Chain Reaction,
pubmed-meshheading:21800645-Transfection
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pubmed:articleTitle |
Effect of glutamine or glucose deprivation on the expression of cyclin and cyclin-dependent kinase genes in glioma cell line U87 and its subline with suppressed activity of signaling enzyme of endoplasmic reticulum-nuclei-1.
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pubmed:affiliation |
Palladin Institute of Biochemistry, National Academy of Science of Ukraine, Kyiv. ominchenko@yahoo.com
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pubmed:publicationType |
Journal Article
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