Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
10
pubmed:dateCreated
2004-5-26
pubmed:abstractText
The cyclin-dependent kinase inhibitor p21 acts as a main executor of p53-induced growth arrest. Recently, a second transcript, p21B, was found to code for a protein expressing proapoptotic activity. We investigated p21 and p21B for mutations and epigenetic silencing in locally advanced breast cancers treated with doxorubicin or 5-fluorouracil/mitomycin and correlated our findings with treatment response and TP53 status.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Antibiotics, Antineoplastic, http://linkedlifedata.com/resource/pubmed/chemical/Antimetabolites, Antineoplastic, http://linkedlifedata.com/resource/pubmed/chemical/DNA Primers, http://linkedlifedata.com/resource/pubmed/chemical/Doxorubicin, http://linkedlifedata.com/resource/pubmed/chemical/Fluorouracil, http://linkedlifedata.com/resource/pubmed/chemical/HRAS protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Mitomycin, http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins p21(ras), http://linkedlifedata.com/resource/pubmed/chemical/RAP2B protein, human, http://linkedlifedata.com/resource/pubmed/chemical/RNA, http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger, http://linkedlifedata.com/resource/pubmed/chemical/Tumor Suppressor Protein p53, http://linkedlifedata.com/resource/pubmed/chemical/rap GTP-Binding Proteins
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
1078-0432
pubmed:author
pubmed:issnType
Print
pubmed:day
15
pubmed:volume
10
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
3438-43
pubmed:dateRevised
2008-11-21
pubmed:meshHeading
pubmed-meshheading:15161699-Antibiotics, Antineoplastic, pubmed-meshheading:15161699-Antimetabolites, Antineoplastic, pubmed-meshheading:15161699-Breast Neoplasms, pubmed-meshheading:15161699-Cell Line, Tumor, pubmed-meshheading:15161699-Cloning, Molecular, pubmed-meshheading:15161699-DNA Methylation, pubmed-meshheading:15161699-DNA Primers, pubmed-meshheading:15161699-Doxorubicin, pubmed-meshheading:15161699-Drug Resistance, Neoplasm, pubmed-meshheading:15161699-Fluorouracil, pubmed-meshheading:15161699-Gene Silencing, pubmed-meshheading:15161699-Humans, pubmed-meshheading:15161699-Immunohistochemistry, pubmed-meshheading:15161699-Lymphocytes, pubmed-meshheading:15161699-Mitomycin, pubmed-meshheading:15161699-Models, Genetic, pubmed-meshheading:15161699-Polymorphism, Genetic, pubmed-meshheading:15161699-Promoter Regions, Genetic, pubmed-meshheading:15161699-Proto-Oncogene Proteins p21(ras), pubmed-meshheading:15161699-RNA, pubmed-meshheading:15161699-RNA, Messenger, pubmed-meshheading:15161699-Reverse Transcriptase Polymerase Chain Reaction, pubmed-meshheading:15161699-Sequence Analysis, DNA, pubmed-meshheading:15161699-Tumor Suppressor Protein p53, pubmed-meshheading:15161699-rap GTP-Binding Proteins
pubmed:year
2004
pubmed:articleTitle
Genetic and epigenetic changes in p21 and p21B do not correlate with resistance to doxorubicin or mitomycin and 5-fluorouracil in locally advanced breast cancer.
pubmed:affiliation
Department of Medicine, Section of Oncology, Haukeland University Hospital, Bergen, Norway.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't