Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
2011-4-7
pubmed:abstractText
Cyclin A, cyclin E, BUBR1, MAD2 and Aurora A are all cell-cycle regulatory proteins and have been proven to play crucial roles in carcinogenesis. However, their expression patterns in invasive ductal breast carcinoma (IDBC) are controversial and unclear. In this study, we examined the expression status of these candidate proteins in a set of 117 invasive ductal carcinomas, and evaluated their associations with known clinicopathological parameters and the expressions of estrogen receptor, progesterone receptor, Ki-67 and Her-2. Univariate and multivariate data analyses both displayed that positive BUBR1 expression was associated with a high Ki-67 labeling index, and negative MAD2 expression was associated with Her-2 overexpression. Positive BUBR1 expression was also associated with a high histological tumor grade in univariate analysis, but not in multivariate analysis. In addition, high Aurora A expression was weakly associated with lymph node metastasis, and cyclin A was strongly associated with the expression of cyclin E in both univariate and multivariate models. In conclusion, this study suggests that evaluation of BUBR1, MAD2 and Aurora A expression levels is likely to improve accuracy of prognostic predictions in IDBC.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Bub1 spindle checkpoint protein, http://linkedlifedata.com/resource/pubmed/chemical/Cell Cycle Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Cyclin A, http://linkedlifedata.com/resource/pubmed/chemical/Cyclin E, http://linkedlifedata.com/resource/pubmed/chemical/MAD2L2 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Protein-Serine-Threonine Kinases, http://linkedlifedata.com/resource/pubmed/chemical/Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Receptor, erbB-2, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Estrogen, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Progesterone, http://linkedlifedata.com/resource/pubmed/chemical/Tumor Markers, Biological, http://linkedlifedata.com/resource/pubmed/chemical/aurora kinase
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
1699-5848
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
26
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
761-8
pubmed:meshHeading
pubmed-meshheading:21472690-Adult, pubmed-meshheading:21472690-Aged, pubmed-meshheading:21472690-Aged, 80 and over, pubmed-meshheading:21472690-Breast Neoplasms, pubmed-meshheading:21472690-Carcinoma, Ductal, Breast, pubmed-meshheading:21472690-Cell Cycle Proteins, pubmed-meshheading:21472690-Cyclin A, pubmed-meshheading:21472690-Cyclin E, pubmed-meshheading:21472690-Female, pubmed-meshheading:21472690-Humans, pubmed-meshheading:21472690-Immunohistochemistry, pubmed-meshheading:21472690-Middle Aged, pubmed-meshheading:21472690-Neoplasm Staging, pubmed-meshheading:21472690-Prognosis, pubmed-meshheading:21472690-Protein-Serine-Threonine Kinases, pubmed-meshheading:21472690-Proteins, pubmed-meshheading:21472690-Receptor, erbB-2, pubmed-meshheading:21472690-Receptors, Estrogen, pubmed-meshheading:21472690-Receptors, Progesterone, pubmed-meshheading:21472690-Tumor Markers, Biological
pubmed:year
2011
pubmed:articleTitle
Expression of cell-cycle regulatory proteins BUBR1, MAD2, Aurora A, cyclin A and cyclin E in invasive ductal breast carcinomas.
pubmed:affiliation
Department of Pathology, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Sino-Austrian Center for Biomarker Discovery, Peking University Health Science Center, Beijing, China.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't