Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:dateCreated
2010-6-18
pubmed:abstractText
Activator protein-2 (AP-2) transcription factors are critically involved in a variety of fundamental cellular processes such as proliferation, differentiation and apoptosis and have also been implicated in carcinogenesis. Expression of the family members AP-2alpha and AP-2gamma is particularly well documented in malignancies of the female breast. Despite increasing evaluation of single AP-2 isoforms in mammary tumors the functional role of concerted expression of multiple AP-2 isoforms in breast cancer remains to be elucidated. AP-2 proteins can form homo- or heterodimers, and there is growing evidence that the net effect whether a cell will proliferate, undergo apoptosis or differentiate is partly dependent on the balance between different AP-2 isoforms.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/20459791-10562268, http://linkedlifedata.com/resource/pubmed/commentcorrection/20459791-10629551, http://linkedlifedata.com/resource/pubmed/commentcorrection/20459791-10748267, http://linkedlifedata.com/resource/pubmed/commentcorrection/20459791-10861472, http://linkedlifedata.com/resource/pubmed/commentcorrection/20459791-11135428, http://linkedlifedata.com/resource/pubmed/commentcorrection/20459791-11137286, http://linkedlifedata.com/resource/pubmed/commentcorrection/20459791-11669459, http://linkedlifedata.com/resource/pubmed/commentcorrection/20459791-11859873, http://linkedlifedata.com/resource/pubmed/commentcorrection/20459791-12226108, http://linkedlifedata.com/resource/pubmed/commentcorrection/20459791-12610102, http://linkedlifedata.com/resource/pubmed/commentcorrection/20459791-12654297, http://linkedlifedata.com/resource/pubmed/commentcorrection/20459791-14573793, http://linkedlifedata.com/resource/pubmed/commentcorrection/20459791-14994922, http://linkedlifedata.com/resource/pubmed/commentcorrection/20459791-15273288, http://linkedlifedata.com/resource/pubmed/commentcorrection/20459791-15467710, http://linkedlifedata.com/resource/pubmed/commentcorrection/20459791-15613452, http://linkedlifedata.com/resource/pubmed/commentcorrection/20459791-15830141, http://linkedlifedata.com/resource/pubmed/commentcorrection/20459791-16199517, http://linkedlifedata.com/resource/pubmed/commentcorrection/20459791-16204029, http://linkedlifedata.com/resource/pubmed/commentcorrection/20459791-16420676, http://linkedlifedata.com/resource/pubmed/commentcorrection/20459791-16533807, http://linkedlifedata.com/resource/pubmed/commentcorrection/20459791-16604184, http://linkedlifedata.com/resource/pubmed/commentcorrection/20459791-16636587, http://linkedlifedata.com/resource/pubmed/commentcorrection/20459791-16761924, http://linkedlifedata.com/resource/pubmed/commentcorrection/20459791-16877704, http://linkedlifedata.com/resource/pubmed/commentcorrection/20459791-17330235, http://linkedlifedata.com/resource/pubmed/commentcorrection/20459791-17947476, http://linkedlifedata.com/resource/pubmed/commentcorrection/20459791-18042070, http://linkedlifedata.com/resource/pubmed/commentcorrection/20459791-18825690, http://linkedlifedata.com/resource/pubmed/commentcorrection/20459791-18922901, http://linkedlifedata.com/resource/pubmed/commentcorrection/20459791-1998122, http://linkedlifedata.com/resource/pubmed/commentcorrection/20459791-8044767, http://linkedlifedata.com/resource/pubmed/commentcorrection/20459791-8134364, http://linkedlifedata.com/resource/pubmed/commentcorrection/20459791-8661133, http://linkedlifedata.com/resource/pubmed/commentcorrection/20459791-8770536, http://linkedlifedata.com/resource/pubmed/commentcorrection/20459791-8895516, http://linkedlifedata.com/resource/pubmed/commentcorrection/20459791-8988173
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
1471-2407
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
10
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
192
pubmed:dateRevised
2010-9-30
pubmed:meshHeading
pubmed-meshheading:20459791-Animals, pubmed-meshheading:20459791-Antineoplastic Agents, pubmed-meshheading:20459791-Apoptosis, pubmed-meshheading:20459791-Cell Line, Tumor, pubmed-meshheading:20459791-Databases, Genetic, pubmed-meshheading:20459791-Drug Resistance, Neoplasm, pubmed-meshheading:20459791-Female, pubmed-meshheading:20459791-Gene Expression Profiling, pubmed-meshheading:20459791-Gene Expression Regulation, Neoplastic, pubmed-meshheading:20459791-Gene Regulatory Networks, pubmed-meshheading:20459791-Mammary Neoplasms, Experimental, pubmed-meshheading:20459791-Mice, pubmed-meshheading:20459791-Mutation, pubmed-meshheading:20459791-Oligonucleotide Array Sequence Analysis, pubmed-meshheading:20459791-Protein Isoforms, pubmed-meshheading:20459791-Radiation Tolerance, pubmed-meshheading:20459791-Receptor, erbB-2, pubmed-meshheading:20459791-Transcription Factor AP-2, pubmed-meshheading:20459791-Transfection
pubmed:year
2010
pubmed:articleTitle
Interference with activator protein-2 transcription factors leads to induction of apoptosis and an increase in chemo- and radiation-sensitivity in breast cancer cells.
pubmed:affiliation
Department of Developmental Pathology, Institute of Pathology, University of Bonn, Medical School, Germany.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't