Linked Life Data

15163307

Source:http://linkedlifedata.com/resource/pubmed/id/15163307

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2004-5-27
pubmed:abstractText
Somatostatin analogs are effective in inhibiting growth of human breast cancer cell lines. These antiproliferative effects are mediated by specific receptors located on cell membranes. The somatostatin receptor subtype 2 (sst2) is the principal mediator of somatostatin effects in normal and cancer cells, and its presence has already been demonstrated in breast cancer. The purpose of our study was to evaluate the clinical relevance of the expression of sst2 by quantifying its mRNA in a large group of infiltrating breast cancers and their corresponding normal tissues. The expression of sst2 mRNA was measured with quantitative real time RT-PCR in 169 breast cancers and in their corresponding unaffected tissues. We evaluated the association of sst2 expression with the commonest clinical-pathologic features of breast cancer. The correlation with a marker of cell proliferation (Ki-67) and with receptor concentration was also evaluated. In cancer tissues, we found that the absolute concentrations of sst2 mRNA were significantly higher in estrogen receptor (ER)-positive samples (P=0.002) as well as in lymph-node-negative cancers (P=0.04) (Student's t-test or one-way ANOVA). In addition, sst2 mRNA was significantly higher in breast cancers than in corresponding unaffected tissues (P=0.0002). However, when the clinical-pathologic parameters were considered, this gradient maintained its statistical significance only in tumors expressing positive prognostic markers, such as the presence of ER (P=0.0005) and progesterone receptors (PgR) (P=0005), and the lack of lymph-node involvement (P=0.0003). The same difference was also significant in postmenopausal women (P=0.001) and in T1 patients (P=0.001). In addition, sst2 mRNA expression was significantly higher (P=0.008) in low-proliferating breast cancers. Finally, we found that the quantitative expression of sst2 mRNA was directly related to the PgR concentration in breast cancer tissues (P<0.001). Our data seem to indicate that an upregulation of sst2 gene expression is a common feature of breast cancers which, on the basis of conventional predictive parameters, are expected to have a better prognosis. Featuring a possible role of somatostatin analogs in combined endocrine therapies for breast cancer, our results seem to confirm that the sst2 status of the tumor should be previously investigated.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
1351-0088
pubmed:author
pubmed:copyrightInfo
Copyright 2004 Society for Endocrinology
pubmed:issnType
Print
pubmed:volume
11
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
323-32
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:15163307-Adult, pubmed-meshheading:15163307-Aged, pubmed-meshheading:15163307-Aged, 80 and over, pubmed-meshheading:15163307-Breast, pubmed-meshheading:15163307-Breast Neoplasms, pubmed-meshheading:15163307-Carcinoma, Ductal, pubmed-meshheading:15163307-Carcinoma, Lobular, pubmed-meshheading:15163307-Cell Proliferation, pubmed-meshheading:15163307-Female, pubmed-meshheading:15163307-Humans, pubmed-meshheading:15163307-In Situ Hybridization, pubmed-meshheading:15163307-Lymph Nodes, pubmed-meshheading:15163307-Neoplasm Invasiveness, pubmed-meshheading:15163307-Neoplasm Staging, pubmed-meshheading:15163307-Prognosis, pubmed-meshheading:15163307-RNA, Messenger, pubmed-meshheading:15163307-Receptors, Estrogen, pubmed-meshheading:15163307-Receptors, Progesterone, pubmed-meshheading:15163307-Receptors, Somatostatin, pubmed-meshheading:15163307-Reverse Transcriptase Polymerase Chain Reaction
pubmed:year
2004
pubmed:articleTitle
Measurement of somatostatin receptor subtype 2 mRNA in breast cancer and corresponding normal tissue.
pubmed:affiliation
Clinical Biochemistry Unit, Department of Clinical Physiopathology, University of Florence, Florence, Italy.
pubmed:publicationType
Journal Article, Comparative Study, Research Support, Non-U.S. Gov't