Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
2003-7-9
pubmed:abstractText
As its role in tumor progression emerges, the PI3K/PKB (Akt) pathway presents an appealing cancer therapeutic target. Recent studies have investigated the mechanisms underlying the tumor-promoting effects of this pathway. PKB triggers a network that positively regulates G1/S cell cycle progression through inactivation of GSK3-beta, leading to increased cyclin D1, and inhibition of Forkhead family transcription factors and the tumor suppressor tuberin (TSC2), leading to reduction of p27Kip1. The identification of p21Waf1/Cip1 and p27Kip1 as novel substrates of PKB provided new insights into mechanisms whereby hyperactivation of this lipid signaling pathway may lead to cell cycle deregulation in human cancers. The PI3K pathway may also play a key role in the G2/M transition and its constitutive activation may lead to defects in DNA damage checkpoint control.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Blood Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Cdkn1a protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/Cdkn1b protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/Cell Cycle Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Cyclin D1, http://linkedlifedata.com/resource/pubmed/chemical/Cyclin-Dependent Kinase Inhibitor..., http://linkedlifedata.com/resource/pubmed/chemical/Cyclin-Dependent Kinase Inhibitor..., http://linkedlifedata.com/resource/pubmed/chemical/Cyclins, http://linkedlifedata.com/resource/pubmed/chemical/Glycogen Synthase Kinase 3, http://linkedlifedata.com/resource/pubmed/chemical/Phosphatidylinositol 3-Kinases, http://linkedlifedata.com/resource/pubmed/chemical/Protein-Serine-Threonine Kinases, http://linkedlifedata.com/resource/pubmed/chemical/Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins c-akt, http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins c-myc, http://linkedlifedata.com/resource/pubmed/chemical/Repressor Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Retinoblastoma-Like Protein p130, http://linkedlifedata.com/resource/pubmed/chemical/Tumor Suppressor Proteins, http://linkedlifedata.com/resource/pubmed/chemical/glycogen synthase kinase 3 beta, http://linkedlifedata.com/resource/pubmed/chemical/tuberous sclerosis complex 2 protein
pubmed:status
MEDLINE
pubmed:issn
1538-4101
pubmed:author
pubmed:issnType
Print
pubmed:volume
2
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
339-45
pubmed:dateRevised
2011-11-2
pubmed:meshHeading
pubmed-meshheading:12851486-Animals, pubmed-meshheading:12851486-Blood Proteins, pubmed-meshheading:12851486-Cell Cycle, pubmed-meshheading:12851486-Cell Cycle Proteins, pubmed-meshheading:12851486-Cyclin D1, pubmed-meshheading:12851486-Cyclin-Dependent Kinase Inhibitor p21, pubmed-meshheading:12851486-Cyclin-Dependent Kinase Inhibitor p27, pubmed-meshheading:12851486-Cyclins, pubmed-meshheading:12851486-Enzyme Activation, pubmed-meshheading:12851486-Glycogen Synthase Kinase 3, pubmed-meshheading:12851486-Mice, pubmed-meshheading:12851486-Phosphatidylinositol 3-Kinases, pubmed-meshheading:12851486-Phosphorylation, pubmed-meshheading:12851486-Protein Interaction Mapping, pubmed-meshheading:12851486-Protein-Serine-Threonine Kinases, pubmed-meshheading:12851486-Proteins, pubmed-meshheading:12851486-Proto-Oncogene Proteins, pubmed-meshheading:12851486-Proto-Oncogene Proteins c-akt, pubmed-meshheading:12851486-Proto-Oncogene Proteins c-myc, pubmed-meshheading:12851486-Repressor Proteins, pubmed-meshheading:12851486-Retinoblastoma-Like Protein p130, pubmed-meshheading:12851486-Signal Transduction, pubmed-meshheading:12851486-Tumor Suppressor Proteins
pubmed:articleTitle
Multiple roles of the PI3K/PKB (Akt) pathway in cell cycle progression.
pubmed:affiliation
Molecular and Cell Biology, Sunnybrook and Women's Health Sciences Centre, University of Toronto, Toronto, Ontario, Canada.
pubmed:publicationType
Journal Article, Review