Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
34
pubmed:dateCreated
2000-8-31
pubmed:abstractText
A key difference among the three structurally similar pRB family members is that only pRB is a tumor suppressor. Identification of distinctive functional differences between pRB and p107/p130 therefore holds promise for a better understanding of the tumor suppression mechanisms of pRB. Enigmatically, pRB and p107 have been shown to have indistinguishable growth suppression activities when studied in the pRB-deficient Saos-2 cell system. In this study, we discovered that, when expressed at physiologically relevant levels, pRB and p107 had distinctive effects in causing growth suppression. pRB induced cellular p130 levels while p107 repressed them. p107, but not pRB, blocked cells inside S phase in addition to G1 arrest. In contrast, no qualitative differences were identified in their abilities to repress the expression of a set of suspected pRB/E2F repression target genes. These results indicate that pRB and p107 possess different growth suppression effects, despite the fact that they have similar E2F repression effects.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/CDC2-CDC28 Kinases, http://linkedlifedata.com/resource/pubmed/chemical/CDK2 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Carrier Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Cell Cycle Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Cyclin-Dependent Kinase 2, http://linkedlifedata.com/resource/pubmed/chemical/Cyclin-Dependent Kinases, http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins, http://linkedlifedata.com/resource/pubmed/chemical/E2F Transcription Factors, http://linkedlifedata.com/resource/pubmed/chemical/Nuclear Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Phosphoproteins, http://linkedlifedata.com/resource/pubmed/chemical/Protein-Serine-Threonine Kinases, http://linkedlifedata.com/resource/pubmed/chemical/Proteins, http://linkedlifedata.com/resource/pubmed/chemical/RBL1 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/RBL2 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Retinoblastoma Protein, http://linkedlifedata.com/resource/pubmed/chemical/Retinoblastoma-Binding Protein 1, http://linkedlifedata.com/resource/pubmed/chemical/Retinoblastoma-Like Protein p107, http://linkedlifedata.com/resource/pubmed/chemical/Retinoblastoma-Like Protein p130, http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factor DP1, http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
0950-9232
pubmed:author
pubmed:issnType
Print
pubmed:day
10
pubmed:volume
19
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
3878-87
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:10951581-Bone Neoplasms, pubmed-meshheading:10951581-CDC2-CDC28 Kinases, pubmed-meshheading:10951581-Carrier Proteins, pubmed-meshheading:10951581-Cell Cycle, pubmed-meshheading:10951581-Cell Cycle Proteins, pubmed-meshheading:10951581-Cyclin-Dependent Kinase 2, pubmed-meshheading:10951581-Cyclin-Dependent Kinases, pubmed-meshheading:10951581-DNA-Binding Proteins, pubmed-meshheading:10951581-E2F Transcription Factors, pubmed-meshheading:10951581-Humans, pubmed-meshheading:10951581-Nuclear Proteins, pubmed-meshheading:10951581-Osteosarcoma, pubmed-meshheading:10951581-Phosphoproteins, pubmed-meshheading:10951581-Protein-Serine-Threonine Kinases, pubmed-meshheading:10951581-Proteins, pubmed-meshheading:10951581-Retinoblastoma Protein, pubmed-meshheading:10951581-Retinoblastoma-Binding Protein 1, pubmed-meshheading:10951581-Retinoblastoma-Like Protein p107, pubmed-meshheading:10951581-Retinoblastoma-Like Protein p130, pubmed-meshheading:10951581-Transcription Factor DP1, pubmed-meshheading:10951581-Transcription Factors, pubmed-meshheading:10951581-Tumor Cells, Cultured
pubmed:year
2000
pubmed:articleTitle
pRB and p107 have distinct effects when expressed in pRB-deficient tumor cells at physiologically relevant levels.
pubmed:affiliation
Department of Developmental and Molecular Biology, Albert Einstein College of Medicine, Bronx, New York 10461, USA.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't