Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
20
pubmed:dateCreated
2009-10-16
pubmed:abstractText
Phosphatase and tensin homologue (PTEN) loss and activation of the Akt-mammalian target of rapamycin (mTOR) pathway increases mRNA translation, increases levels of the antiapoptotic protein FLIP(S), and confers resistance to tumor necrosis factor-related apoptosis-inducing ligand (TRAIL)-induced apoptosis in glioblastoma multiforme (GBM). In PTEN-deficient GBM cells, however, the FLIP(S) protein also exhibited a longer half-life than in PTEN mutant GBM cells, and this longer half-life correlated with decreased FLIP(S) polyubiquitination. FLIP(S) half-life in PTEN mutant GBM cells was reduced by exposure to an Akt inhibitor, but not to rapamycin, suggesting the existence of a previously undescribed, mTOR-independent linkage between PTEN and the ubiquitin-dependent control of protein stability. Total levels of the candidate FLIP(S) E3 ubiquitin ligase atrophin-interacting protein 4 (AIP4) were comparable in PTEN wild-type (WT) and PTEN mutant GBM cells, although in PTEN-deficient cells, AIP4 was maintained in a stable polyubiquitinated state that was less able to associate with FLIP(S) or with the FLIP(S)-containing death inducing signal complex. Small interfering RNA-mediated suppression of AIP4 levels in PTEN WT cells decreased FLIP(S) ubiquitination, prolonged FLIP(S) half-life, and increased TRAIL resistance. Similarly, the Akt activation that was previously shown to increase TRAIL resistance did not alter AIP4 levels, but increased AIP4 ubiquitination, increased FLIP(S) steady-state levels, and suppressed FLIP(S) ubiquitination. These results define the PTEN-Akt-AIP4 pathway as a key regulator of FLIP(S) ubiquitination, FLIP(S) stability, and TRAIL sensitivity and also define a novel link between PTEN and the ubiquitin-mediated control of protein stability.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/CASP8 and FADD-Like Apoptosis..., http://linkedlifedata.com/resource/pubmed/chemical/ITCH protein, human, http://linkedlifedata.com/resource/pubmed/chemical/MTOR protein, human, http://linkedlifedata.com/resource/pubmed/chemical/PTEN Phosphohydrolase, http://linkedlifedata.com/resource/pubmed/chemical/Protein Kinases, http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins c-akt, http://linkedlifedata.com/resource/pubmed/chemical/RNA, Small Interfering, http://linkedlifedata.com/resource/pubmed/chemical/Repressor Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Sirolimus, http://linkedlifedata.com/resource/pubmed/chemical/TNF-Related Apoptosis-Inducing..., http://linkedlifedata.com/resource/pubmed/chemical/TOR Serine-Threonine Kinases, http://linkedlifedata.com/resource/pubmed/chemical/Ubiquitin, http://linkedlifedata.com/resource/pubmed/chemical/Ubiquitin-Protein Ligases, http://linkedlifedata.com/resource/pubmed/chemical/mTOR protein, mouse
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
1538-7445
pubmed:author
pubmed:issnType
Electronic
pubmed:day
15
pubmed:volume
69
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
7911-6
pubmed:dateRevised
2011-9-22
pubmed:meshHeading
pubmed-meshheading:19808964-Animals, pubmed-meshheading:19808964-Apoptosis, pubmed-meshheading:19808964-Blotting, Western, pubmed-meshheading:19808964-CASP8 and FADD-Like Apoptosis Regulating Protein, pubmed-meshheading:19808964-Cell Line, Tumor, pubmed-meshheading:19808964-Drug Resistance, Neoplasm, pubmed-meshheading:19808964-Glioblastoma, pubmed-meshheading:19808964-Half-Life, pubmed-meshheading:19808964-Humans, pubmed-meshheading:19808964-Immunoprecipitation, pubmed-meshheading:19808964-Mice, pubmed-meshheading:19808964-Mice, Knockout, pubmed-meshheading:19808964-PTEN Phosphohydrolase, pubmed-meshheading:19808964-Protein Kinases, pubmed-meshheading:19808964-Proto-Oncogene Proteins c-akt, pubmed-meshheading:19808964-RNA, Small Interfering, pubmed-meshheading:19808964-Repressor Proteins, pubmed-meshheading:19808964-Signal Transduction, pubmed-meshheading:19808964-Sirolimus, pubmed-meshheading:19808964-TNF-Related Apoptosis-Inducing Ligand, pubmed-meshheading:19808964-TOR Serine-Threonine Kinases, pubmed-meshheading:19808964-Ubiquitin, pubmed-meshheading:19808964-Ubiquitin-Protein Ligases, pubmed-meshheading:19808964-Ubiquitination, pubmed-meshheading:19808964-Xenograft Model Antitumor Assays
pubmed:year
2009
pubmed:articleTitle
A novel PTEN-dependent link to ubiquitination controls FLIPS stability and TRAIL sensitivity in glioblastoma multiforme.
pubmed:affiliation
Brain Tumor Research Center, Department of Neurological Surgery and University of California San Francisco Comprehensive Cancer Center, University of California San Francisco, San Francisco, California 94158-9001, USA.
pubmed:publicationType
Journal Article, Research Support, N.I.H., Extramural