Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
1994-7-7
pubmed:abstractText
Membrane-associated phospholipase A2 (M-PLA2) is an enzyme that hydrolyses the sn-2 fatty acyl ester bond of phosphoglycerides. We measured M-PLA2 concentration in tissue extracts from 325 human breast cancers using a specific radioimmunoassay recently developed. Correlation analyses between the tissue concentration of M-PLA2 and clinicopathological factors showed that the enzyme level was significantly higher in patients with distant metastasis than in those without. In addition, M-PLA2 concentration was significantly higher in scirrhous carcinoma than in other histological types. No significant association was found between M-PLA2 concentration and age, menstrual status, tumour size, histological grade, vessel involvement or oestrogen receptor (ER) and progesterone receptor (PR) status. The expression of M-PLA2 mRNA was examined in a fibroadenoma, a stage IV breast cancer and its metastatic site of skin. Northern blot analysis showed a clear hybridisation band corresponding to M-PLA2 mRNA in both primary breast cancer and its metastatic site, while the fibroadenoma expressed a faint band corresponding to M-PLA2 mRNA. Breast cancer patients with high M-PLA2 concentrations exhibited significantly shorter disease-free and overall survival than those with low M-PLA2 concentration at the cut-off point of 5 ng 100 mg-1 protein, which was determined in a separate study. In multivariate analysis, M-PLA2 was found to be an independent prognostic factor for disease recurrence and death in human breast cancer. The possible significance of M-PLA2 expression in human breast cancer tissue is discussed.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/8198986-13499785, http://linkedlifedata.com/resource/pubmed/commentcorrection/8198986-14450081, http://linkedlifedata.com/resource/pubmed/commentcorrection/8198986-1462048, http://linkedlifedata.com/resource/pubmed/commentcorrection/8198986-1698992, http://linkedlifedata.com/resource/pubmed/commentcorrection/8198986-1726681, http://linkedlifedata.com/resource/pubmed/commentcorrection/8198986-1761509, http://linkedlifedata.com/resource/pubmed/commentcorrection/8198986-2065320, http://linkedlifedata.com/resource/pubmed/commentcorrection/8198986-2119883, http://linkedlifedata.com/resource/pubmed/commentcorrection/8198986-2296271, http://linkedlifedata.com/resource/pubmed/commentcorrection/8198986-2386981, http://linkedlifedata.com/resource/pubmed/commentcorrection/8198986-2471196, http://linkedlifedata.com/resource/pubmed/commentcorrection/8198986-2572788, http://linkedlifedata.com/resource/pubmed/commentcorrection/8198986-2572846, http://linkedlifedata.com/resource/pubmed/commentcorrection/8198986-2775276, http://linkedlifedata.com/resource/pubmed/commentcorrection/8198986-2925608, http://linkedlifedata.com/resource/pubmed/commentcorrection/8198986-3082829, http://linkedlifedata.com/resource/pubmed/commentcorrection/8198986-3132609, http://linkedlifedata.com/resource/pubmed/commentcorrection/8198986-3531715, http://linkedlifedata.com/resource/pubmed/commentcorrection/8198986-6229053, http://linkedlifedata.com/resource/pubmed/commentcorrection/8198986-6252969, http://linkedlifedata.com/resource/pubmed/commentcorrection/8198986-6883208, http://linkedlifedata.com/resource/pubmed/commentcorrection/8198986-837364, http://linkedlifedata.com/resource/pubmed/commentcorrection/8198986-8431369, http://linkedlifedata.com/resource/pubmed/commentcorrection/8198986-8490834, http://linkedlifedata.com/resource/pubmed/commentcorrection/8198986-873920
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
0007-0920
pubmed:author
pubmed:issnType
Print
pubmed:volume
69
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1166-70
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed-meshheading:8198986-Age Factors, pubmed-meshheading:8198986-Analysis of Variance, pubmed-meshheading:8198986-Blotting, Northern, pubmed-meshheading:8198986-Breast Neoplasms, pubmed-meshheading:8198986-Female, pubmed-meshheading:8198986-Follow-Up Studies, pubmed-meshheading:8198986-Gene Expression, pubmed-meshheading:8198986-Humans, pubmed-meshheading:8198986-Middle Aged, pubmed-meshheading:8198986-Multivariate Analysis, pubmed-meshheading:8198986-Neoplasm Metastasis, pubmed-meshheading:8198986-Phospholipases A, pubmed-meshheading:8198986-Phospholipases A2, pubmed-meshheading:8198986-Prognosis, pubmed-meshheading:8198986-RNA, Messenger, pubmed-meshheading:8198986-Receptors, Estrogen, pubmed-meshheading:8198986-Receptors, Progesterone, pubmed-meshheading:8198986-Survival Analysis, pubmed-meshheading:8198986-Time Factors
pubmed:year
1994
pubmed:articleTitle
Overexpression of group II phospholipase A2 in human breast cancer tissues is closely associated with their malignant potency.
pubmed:affiliation
Department of Surgery II, Kumamoto University Medical School, Japan.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't