Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:dateCreated
2009-7-31
pubmed:abstractText
Aberrant hypermethylation of gene promoter regions is one of the mechanisms for inactivation of tumour suppressor genes in many human cancers including breast carcinoma. In the current study, we aimed to assess by MSP, the methylation pattern of two cancer-related genes involved in DNA repair: hMLH1 (mutL homolog 1, colon cancer, nonpolyposis type 2 (E. coli) and BRCA1 (breast cancer 1, early onset) in 78 primary breast cancers from Tunisian patients. The methylation frequencies were 24.36% for hMLH1 and 46% for BRCA1. BRCA1 methylation correlated with age at diagnosis (P = .015) and 5-years disease free survival (P = .016) while hMLH1 methylation was more frequent in larger tumors (P = .002) and in presence of distant metastasis (P = .004). Furthermore, methylation of hMLH1 significantly correlated with high level of P53 expression (P = .006) and with overall survival (P = .015) suggesting that silencing of hMLH1 through aberrant promoter methylation could be used as a poor prognosis indicator in breast cancer.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/19644562-10208417, http://linkedlifedata.com/resource/pubmed/commentcorrection/19644562-10657950, http://linkedlifedata.com/resource/pubmed/commentcorrection/19644562-11309270, http://linkedlifedata.com/resource/pubmed/commentcorrection/19644562-11501575, http://linkedlifedata.com/resource/pubmed/commentcorrection/19644562-11839581, http://linkedlifedata.com/resource/pubmed/commentcorrection/19644562-12154405, http://linkedlifedata.com/resource/pubmed/commentcorrection/19644562-12154408, http://linkedlifedata.com/resource/pubmed/commentcorrection/19644562-12173039, http://linkedlifedata.com/resource/pubmed/commentcorrection/19644562-12191635, http://linkedlifedata.com/resource/pubmed/commentcorrection/19644562-15172987, http://linkedlifedata.com/resource/pubmed/commentcorrection/19644562-15313416, http://linkedlifedata.com/resource/pubmed/commentcorrection/19644562-15447983, http://linkedlifedata.com/resource/pubmed/commentcorrection/19644562-15890247, http://linkedlifedata.com/resource/pubmed/commentcorrection/19644562-16029926, http://linkedlifedata.com/resource/pubmed/commentcorrection/19644562-16185815, http://linkedlifedata.com/resource/pubmed/commentcorrection/19644562-16322213, http://linkedlifedata.com/resource/pubmed/commentcorrection/19644562-16769596, http://linkedlifedata.com/resource/pubmed/commentcorrection/19644562-16909910, http://linkedlifedata.com/resource/pubmed/commentcorrection/19644562-17071074, http://linkedlifedata.com/resource/pubmed/commentcorrection/19644562-17611401, http://linkedlifedata.com/resource/pubmed/commentcorrection/19644562-18173856, http://linkedlifedata.com/resource/pubmed/commentcorrection/19644562-18205041, http://linkedlifedata.com/resource/pubmed/commentcorrection/19644562-18329696, http://linkedlifedata.com/resource/pubmed/commentcorrection/19644562-18521744, http://linkedlifedata.com/resource/pubmed/commentcorrection/19644562-19008097, http://linkedlifedata.com/resource/pubmed/commentcorrection/19644562-7448713, http://linkedlifedata.com/resource/pubmed/commentcorrection/19644562-8492317, http://linkedlifedata.com/resource/pubmed/commentcorrection/19644562-8657182, http://linkedlifedata.com/resource/pubmed/commentcorrection/19644562-8790415, http://linkedlifedata.com/resource/pubmed/commentcorrection/19644562-9727085
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
1110-7251
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
2009
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
369129
pubmed:dateRevised
2010-11-18
pubmed:meshHeading
pubmed-meshheading:19644562-Adaptor Proteins, Signal Transducing, pubmed-meshheading:19644562-Adult, pubmed-meshheading:19644562-African Continental Ancestry Group, pubmed-meshheading:19644562-Aged, pubmed-meshheading:19644562-BRCA1 Protein, pubmed-meshheading:19644562-Breast Neoplasms, pubmed-meshheading:19644562-DNA, Neoplasm, pubmed-meshheading:19644562-DNA Methylation, pubmed-meshheading:19644562-Female, pubmed-meshheading:19644562-Gene Silencing, pubmed-meshheading:19644562-Genes, Neoplasm, pubmed-meshheading:19644562-Humans, pubmed-meshheading:19644562-Immunohistochemistry, pubmed-meshheading:19644562-Kaplan-Meier Estimate, pubmed-meshheading:19644562-Middle Aged, pubmed-meshheading:19644562-Multivariate Analysis, pubmed-meshheading:19644562-Neoplasm Invasiveness, pubmed-meshheading:19644562-Nuclear Proteins, pubmed-meshheading:19644562-Promoter Regions, Genetic, pubmed-meshheading:19644562-Tumor Suppressor Protein p53, pubmed-meshheading:19644562-Tunisia
pubmed:year
2009
pubmed:articleTitle
Clinical significance of epigenetic inactivation of hMLH1 and BRCA1 in Tunisian patients with invasive breast carcinoma.
pubmed:affiliation
Unitéde Génétique du cancer et Production de protéines thérapeutiques, Centre de Biotechnologie de Sfax, route Sidi Mansour, BP 1177, 3018 Sfax, Tunisia.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't