Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
9-10
pubmed:dateCreated
1999-4-15
pubmed:abstractText
Human breast carcinoma is biologically heterogeneous, and its clinical course may vary from an indolent slowly progressive one to a course associated with rapid progression and metastatic spread. It is important to establish prognostic factors which will define subgroups of patients with low vs high risk of recurrence so as to better define the need for additional therapy. Additional characterization of the molecular make-up of breast cancer phenotypes should provide important insights into the biology of breast cancer. In the present study, we investigated apoptosis, expression of p27Kip1 and p53 retrospectively in 181 human breast cancer specimens. In addition, their relevance to the biological behaviour of breast cancer was examined. Our studies found a significant association among high histological grade, high p53, low apoptosis and low p27. Our results also demonstrated that, in human breast cancer, low levels of p27 and apoptotic index (AI) strongly correlated with the presence of lymph node metastasis and decreased patient survival. In node-negative patients, however, p27 also had prognostic value for relapse-free and overall survival in multivariate analysis. Furthermore p27 and AI had predictive value for the benefits of chemotherapy. These latter observations should prompt prospective randomized studies designed to investigate the predictive role of p27 and AI in determining who should receive chemotherapy in node-negative patients.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/10188908-1394123, http://linkedlifedata.com/resource/pubmed/commentcorrection/10188908-1557121, http://linkedlifedata.com/resource/pubmed/commentcorrection/10188908-1625055, http://linkedlifedata.com/resource/pubmed/commentcorrection/10188908-3415687, http://linkedlifedata.com/resource/pubmed/commentcorrection/10188908-7601561, http://linkedlifedata.com/resource/pubmed/commentcorrection/10188908-7649471, http://linkedlifedata.com/resource/pubmed/commentcorrection/10188908-7796420, http://linkedlifedata.com/resource/pubmed/commentcorrection/10188908-7911228, http://linkedlifedata.com/resource/pubmed/commentcorrection/10188908-7997877, http://linkedlifedata.com/resource/pubmed/commentcorrection/10188908-8033212, http://linkedlifedata.com/resource/pubmed/commentcorrection/10188908-8033213, http://linkedlifedata.com/resource/pubmed/commentcorrection/10188908-8125163, http://linkedlifedata.com/resource/pubmed/commentcorrection/10188908-8242751, http://linkedlifedata.com/resource/pubmed/commentcorrection/10188908-8242752, http://linkedlifedata.com/resource/pubmed/commentcorrection/10188908-8259207, http://linkedlifedata.com/resource/pubmed/commentcorrection/10188908-8288131, http://linkedlifedata.com/resource/pubmed/commentcorrection/10188908-8649834, http://linkedlifedata.com/resource/pubmed/commentcorrection/10188908-8774478, http://linkedlifedata.com/resource/pubmed/commentcorrection/10188908-9018243, http://linkedlifedata.com/resource/pubmed/commentcorrection/10188908-9018244, http://linkedlifedata.com/resource/pubmed/commentcorrection/10188908-9018245, http://linkedlifedata.com/resource/pubmed/commentcorrection/10188908-9039259, http://linkedlifedata.com/resource/pubmed/commentcorrection/10188908-9044834, http://linkedlifedata.com/resource/pubmed/commentcorrection/10188908-9067571, http://linkedlifedata.com/resource/pubmed/commentcorrection/10188908-9102210, http://linkedlifedata.com/resource/pubmed/commentcorrection/10188908-9270000, http://linkedlifedata.com/resource/pubmed/commentcorrection/10188908-9306959, http://linkedlifedata.com/resource/pubmed/commentcorrection/10188908-9355976, http://linkedlifedata.com/resource/pubmed/commentcorrection/10188908-9377601, http://linkedlifedata.com/resource/pubmed/commentcorrection/10188908-9407946
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
0007-0920
pubmed:author
pubmed:issnType
Print
pubmed:volume
79
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1572-8
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed-meshheading:10188908-Analysis of Variance, pubmed-meshheading:10188908-Apoptosis, pubmed-meshheading:10188908-Breast Neoplasms, pubmed-meshheading:10188908-Cell Cycle Proteins, pubmed-meshheading:10188908-Cyclin-Dependent Kinase Inhibitor p27, pubmed-meshheading:10188908-Disease-Free Survival, pubmed-meshheading:10188908-Female, pubmed-meshheading:10188908-Follow-Up Studies, pubmed-meshheading:10188908-Humans, pubmed-meshheading:10188908-Lymphatic Metastasis, pubmed-meshheading:10188908-Microtubule-Associated Proteins, pubmed-meshheading:10188908-Middle Aged, pubmed-meshheading:10188908-Phenotype, pubmed-meshheading:10188908-Prognosis, pubmed-meshheading:10188908-Proportional Hazards Models, pubmed-meshheading:10188908-Survival Rate, pubmed-meshheading:10188908-Tumor Suppressor Protein p53, pubmed-meshheading:10188908-Tumor Suppressor Proteins
pubmed:year
1999
pubmed:articleTitle
Prognostic role of p27Kip1 and apoptosis in human breast cancer.
pubmed:affiliation
Department of Surgery, Cancer Hospital/Cancer Institute, Shanghai Medical University, People's Republic of China.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't