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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
17
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pubmed:dateCreated |
2001-4-24
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pubmed:abstractText |
The Id proteins play an important role in proliferation, differentiation, and tumor development. We report here that Id gene expression can be regulated by the insulin-like growth factor I receptor (IGF-IR), a receptor that also participates in the regulation of cellular proliferation and differentiation. Specifically, we found that the IGF-IR activated by its ligand was a strong inducer of Id2 gene expression in 32D murine hemopoietic cells. This activation was not simply the result of cellular proliferation, as Id2 gene expression was higher in 32D cells stimulated by IGF-I than in cells exponentially growing in interleukin-3. The up-regulation of Id2 gene expression was largely dependent on the presence of insulin receptor substrate-1, a major substrate of the IGF-IR and a potent activator of the phosphatidylinositol 3-kinase (PI3K) pathway. The role of PI3K activity in the up-regulation of Id2 gene expression by the IGF-IR was confirmed by different methods and in different cell types. In 32D cells, the up-regulation of Id2 gene expression by the PI3K pathway correlated with interleukin-3 independence and inhibition of differentiation.
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pubmed:grant |
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/ID2 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/IRS1 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Idb2 protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/Inhibitor of Differentiation...,
http://linkedlifedata.com/resource/pubmed/chemical/Insulin Receptor Substrate Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-3,
http://linkedlifedata.com/resource/pubmed/chemical/Irs1 protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/Ligands,
http://linkedlifedata.com/resource/pubmed/chemical/PTEN Phosphohydrolase,
http://linkedlifedata.com/resource/pubmed/chemical/PTEN protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Phosphatidylinositol 3-Kinases,
http://linkedlifedata.com/resource/pubmed/chemical/Phosphoproteins,
http://linkedlifedata.com/resource/pubmed/chemical/Phosphoric Monoester Hydrolases,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/Receptor, IGF Type 1,
http://linkedlifedata.com/resource/pubmed/chemical/Repressor Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors,
http://linkedlifedata.com/resource/pubmed/chemical/Tumor Suppressor Proteins
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
0021-9258
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:day |
27
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pubmed:volume |
276
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
13867-74
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:11278691-Animals,
pubmed-meshheading:11278691-Blotting, Northern,
pubmed-meshheading:11278691-Blotting, Western,
pubmed-meshheading:11278691-Cell Differentiation,
pubmed-meshheading:11278691-Cell Division,
pubmed-meshheading:11278691-Cell Line,
pubmed-meshheading:11278691-DNA-Binding Proteins,
pubmed-meshheading:11278691-Gene Expression Regulation,
pubmed-meshheading:11278691-Humans,
pubmed-meshheading:11278691-Inhibitor of Differentiation Protein 2,
pubmed-meshheading:11278691-Insulin Receptor Substrate Proteins,
pubmed-meshheading:11278691-Interleukin-3,
pubmed-meshheading:11278691-Ligands,
pubmed-meshheading:11278691-Mice,
pubmed-meshheading:11278691-PTEN Phosphohydrolase,
pubmed-meshheading:11278691-Phosphatidylinositol 3-Kinases,
pubmed-meshheading:11278691-Phosphoproteins,
pubmed-meshheading:11278691-Phosphoric Monoester Hydrolases,
pubmed-meshheading:11278691-Plasmids,
pubmed-meshheading:11278691-Protein Structure, Tertiary,
pubmed-meshheading:11278691-RNA, Messenger,
pubmed-meshheading:11278691-Receptor, IGF Type 1,
pubmed-meshheading:11278691-Repressor Proteins,
pubmed-meshheading:11278691-Retroviridae,
pubmed-meshheading:11278691-Signal Transduction,
pubmed-meshheading:11278691-Time Factors,
pubmed-meshheading:11278691-Transcription Factors,
pubmed-meshheading:11278691-Tumor Cells, Cultured,
pubmed-meshheading:11278691-Tumor Suppressor Proteins,
pubmed-meshheading:11278691-Up-Regulation
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pubmed:year |
2001
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pubmed:articleTitle |
Regulation of Id2 gene expression by the insulin-like growth factor I receptor requires signaling by phosphatidylinositol 3-kinase.
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pubmed:affiliation |
Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, Pennsylvania 19107, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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