rdf:type |
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lifeskim:mentions |
umls-concept:C0007600,
umls-concept:C0017262,
umls-concept:C0033640,
umls-concept:C0079460,
umls-concept:C0086418,
umls-concept:C0185117,
umls-concept:C0684249,
umls-concept:C0812202,
umls-concept:C1314939,
umls-concept:C1518174,
umls-concept:C2911684
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pubmed:issue |
1
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pubmed:dateCreated |
2003-3-20
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pubmed:abstractText |
Granulocyte-macrophage colony-stimulating factor (GM-CSF) is a cytokine expressed in the non-small lung carcinoma cells (NSCLC). However, transcriptional regulation of GM-CSF is not well characterized in NSCLC. In this study we found that two cis-acting ETS family consensus sites are important for transcriptional regulation of GM-CSF in A549 human lung carcinoma cells. These two sites are located separately at around -40 and -100 bp from the transcription start site. Results of transient transfection assays with A549 cells indicated that ETS2 had a strong positive effect on GM-CSF promoter activity. Furthermore, this activity was enhanced by protein kinase C activator, phorbol 12-myristate 13-acetate (PMA), in an ETS consensus-dependent manner, while PMA could also enhance the expression level of ETS2. The protein kinase C inhibitors decreased GM-CSF promoter activity induced by the protein kinase C activator PMA. We also found that antisense ETS2 mRNA decreased PMA-induced GM-CSF promoter activity, supporting the possibility that ETS2 is involved in protein kinase C-induced GM-CSF transcriptional function. Endogenous expression of GM-CSF mRNA was increased by ETS2 transfection and the increased expression was further enhanced by PMA. These data indicate that GM-CSF is up-regulated by ETS2, a target of protein kinase C.
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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/DNA-Binding Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/ERF protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/ETS2 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Granulocyte-Macrophage...,
http://linkedlifedata.com/resource/pubmed/chemical/Protein Kinase C,
http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Protein c-ets-2,
http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Repressor Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Trans-Activators,
http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
|
pubmed:issn |
0006-291X
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pubmed:author |
|
pubmed:issnType |
Print
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pubmed:day |
28
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pubmed:volume |
303
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
190-5
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:12646185-Blotting, Western,
pubmed-meshheading:12646185-Carcinoma, Non-Small-Cell Lung,
pubmed-meshheading:12646185-DNA-Binding Proteins,
pubmed-meshheading:12646185-Enzyme Activation,
pubmed-meshheading:12646185-Granulocyte-Macrophage Colony-Stimulating Factor,
pubmed-meshheading:12646185-Humans,
pubmed-meshheading:12646185-Lung Neoplasms,
pubmed-meshheading:12646185-Plasmids,
pubmed-meshheading:12646185-Promoter Regions, Genetic,
pubmed-meshheading:12646185-Protein Binding,
pubmed-meshheading:12646185-Protein Kinase C,
pubmed-meshheading:12646185-Proto-Oncogene Protein c-ets-2,
pubmed-meshheading:12646185-Proto-Oncogene Proteins,
pubmed-meshheading:12646185-Repressor Proteins,
pubmed-meshheading:12646185-Reverse Transcriptase Polymerase Chain Reaction,
pubmed-meshheading:12646185-Trans-Activators,
pubmed-meshheading:12646185-Transcription Factors,
pubmed-meshheading:12646185-Transcriptional Activation,
pubmed-meshheading:12646185-Transfection,
pubmed-meshheading:12646185-Tumor Cells, Cultured,
pubmed-meshheading:12646185-Up-Regulation
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pubmed:year |
2003
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pubmed:articleTitle |
ETS2 is involved in protein kinase C-activated expression of granulocyte-macrophage colony-stimulating factor in human non-small lung carcinoma cell line, A549.
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pubmed:affiliation |
Department of Molecular Medicine, Graduate School of Pharmaceutical Sciences, Kumamoto University, 5-1 Oe-honmachi, Kumamoto 862-0973, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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