Source:http://linkedlifedata.com/resource/pubmed/id/11534179
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rdf:type | |
lifeskim:mentions |
umls-concept:C0007600,
umls-concept:C0035544,
umls-concept:C0035668,
umls-concept:C0205360,
umls-concept:C0205369,
umls-concept:C0208355,
umls-concept:C0242275,
umls-concept:C0332256,
umls-concept:C0441712,
umls-concept:C0851285,
umls-concept:C1148807,
umls-concept:C1167298,
umls-concept:C1998811,
umls-concept:C2347930
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pubmed:issue |
6
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pubmed:dateCreated |
2001-9-5
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pubmed:abstractText |
A comparative study was made of reactive oxygen species (ROS) in rat embryo fibroblasts and their transformants. Primary rat embryo fibroblasts (REF), REF transformed by the complementing oncogenes E1A plus cHa-ras (cell line E1A + Ras), and REF transformed by E1A plus E1B-19 kDa (cell line E1A + E1B) were studied. ROS generation was measured with microfluorometric assay using fluorescent probe 2',7'-dichlorofluorescin diacetate. It has been shown that the block of REF and E1A + 1B cells in the G1/S under serum-starved conditions (0.5% serum) for 24-48 h was paralleled by a decrease in ROS generation. Activation of serum-starved REF and E1A + 1B cells with 10% serum resulted in reactivation of cell cycle and gradual increase in ROS generation. The maximum intracellular level of ROS correlated in time with the phase of DNA synthesis. Serum-starved E1A + Ras cells were not stopped in the G1/S and ROS production of these cells was not dependent on serum growth factors. The prolonged cultivation of E1A + Ras cells in the medium with low serum content (0.5%) caused a sharp increase in ROS generation, which was accompanied by apoptotic death.
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pubmed:language |
rus
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/3' Untranslated Regions,
http://linkedlifedata.com/resource/pubmed/chemical/Endoribonucleases,
http://linkedlifedata.com/resource/pubmed/chemical/Epidermal Growth Factor,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/Ribonucleoproteins, Small Nuclear
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pubmed:status |
MEDLINE
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pubmed:issn |
0041-3771
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
43
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
595-601
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:11534179-3' Untranslated Regions,
pubmed-meshheading:11534179-Endoribonucleases,
pubmed-meshheading:11534179-Epidermal Growth Factor,
pubmed-meshheading:11534179-Humans,
pubmed-meshheading:11534179-Molecular Weight,
pubmed-meshheading:11534179-RNA, Messenger,
pubmed-meshheading:11534179-Ribonucleoproteins, Small Nuclear,
pubmed-meshheading:11534179-Signal Transduction,
pubmed-meshheading:11534179-Tumor Cells, Cultured
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pubmed:year |
2001
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pubmed:articleTitle |
[Specific regulated endonuclease activity of small RNP, containing prosomes from the A431 cell line: possible mechanisms of regulating the stability of RNA by epidermal growth factor].
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pubmed:affiliation |
Institute of Cytology RAS, St. Petersburg.
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pubmed:publicationType |
Journal Article,
English Abstract
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