Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
29
pubmed:dateCreated
2000-8-16
pubmed:abstractText
The c-myc gene is frequently over-expressed in human cancers and is involved in regulation of proliferation, differentiation and apoptosis. c-Myc is a transcription factor that acts primarily by regulating the expression of other genes. However, it has been very difficult to identify bona fide c-Myc target genes that explain its diverse biological activities. The recent generation of c-myc deficient Rat1A fibroblasts with a profound and stable growth defect provides a new system to search for genes that can substitute for c-myc in proliferation. In this study, we have attempted to identify genes that rescue the slow growth phenotype of c-myc null cells through introduction of a series of potent cell cycle regulatory genes and several retroviral cDNA expression libraries. None of the candidate genes tested, including SV40 T-antigen and adenovirus E1A, caused reversal of the c-myc null growth defect. Furthermore, extensive screens with high-complexity retroviral cDNA libraries from three different tissue sources revealed that only c-myc and N-myc rescued the c-myc null slow-growth phenotype. Our data support the notion that there are no functional equivalents of the myc family of proto-oncogenes and also suggest that there are no c-Myc-activated genes that alone can substitute for c-Myc in control of cell proliferation.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Adenovirus E1A Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Antigens, Polyomavirus Transforming, http://linkedlifedata.com/resource/pubmed/chemical/Arid4a protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/Carrier Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Cell Cycle Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Cyclin D1, http://linkedlifedata.com/resource/pubmed/chemical/Cyclin E, http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins, http://linkedlifedata.com/resource/pubmed/chemical/E2F Transcription Factors, http://linkedlifedata.com/resource/pubmed/chemical/E2F2 Transcription Factor, http://linkedlifedata.com/resource/pubmed/chemical/E2F3 Transcription Factor, http://linkedlifedata.com/resource/pubmed/chemical/E2F3 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/E2f3 protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins c-myc, http://linkedlifedata.com/resource/pubmed/chemical/Retinoblastoma-Binding Protein 1, http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factor DP1, http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
0950-9232
pubmed:author
pubmed:issnType
Print
pubmed:day
6
pubmed:volume
19
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
3330-4
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:10918589-Adenovirus E1A Proteins, pubmed-meshheading:10918589-Animals, pubmed-meshheading:10918589-Antigens, Polyomavirus Transforming, pubmed-meshheading:10918589-Carrier Proteins, pubmed-meshheading:10918589-Cell Cycle Proteins, pubmed-meshheading:10918589-Cell Division, pubmed-meshheading:10918589-Cell Line, pubmed-meshheading:10918589-Cyclin D1, pubmed-meshheading:10918589-Cyclin E, pubmed-meshheading:10918589-DNA-Binding Proteins, pubmed-meshheading:10918589-E2F Transcription Factors, pubmed-meshheading:10918589-E2F2 Transcription Factor, pubmed-meshheading:10918589-E2F3 Transcription Factor, pubmed-meshheading:10918589-Fibroblasts, pubmed-meshheading:10918589-Helix-Loop-Helix Motifs, pubmed-meshheading:10918589-Humans, pubmed-meshheading:10918589-K562 Cells, pubmed-meshheading:10918589-Leucine Zippers, pubmed-meshheading:10918589-Mice, pubmed-meshheading:10918589-Proto-Oncogene Proteins c-myc, pubmed-meshheading:10918589-Rats, pubmed-meshheading:10918589-Retinoblastoma-Binding Protein 1, pubmed-meshheading:10918589-Transcription Factor DP1, pubmed-meshheading:10918589-Transcription Factors
pubmed:year
2000
pubmed:articleTitle
A genetic screen to identify genes that rescue the slow growth phenotype of c-myc null fibroblasts.
pubmed:affiliation
Division of Molecular Carcinogenesis, and Center for Biomedical Genetics, The Netherlands Cancer Institute, Amsterdam.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't