Source:http://linkedlifedata.com/resource/pubmed/id/15923160
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
|
pubmed:dateCreated |
2005-5-30
|
pubmed:abstractText |
We conducted this study to ascertain the prevalence of erb-b2 gene amplification in breast cancer specimens read as 2+ in immunohistochemical analysis. Slides from patients with metastatic or recurrent breast cancer were eligible for fluorescent in situ hybridization (FISH) study if they were read as 2+ immunohistochemically for erb-b2 by a certified pathologist. The PathVysion kit (Vysis, Downers Grove, IL) was used for FISH studies. Amplification of the erb-b2 gene was defined as an erb-b2/CEP17 (chromosome 17 centromere) ratio of 2 or more in 30 tumor cells counted. From May 2003 to June 2004, 221 slides were submitted from 24 hospitals around the island. Of 216 successful hybridizations, 96 (44.4%) were determined to be erb-b2 amplified. In addition, the topoisomerase IIa gene was coamplified in 11 (21%) of 53 and deleted in 8 (15%) of 53 erb-b2 amplified cases. The erb-b2 gene amplification rate was very high in cases determined to be 2+ by immunohistochemical analysis; therefore, determination of erb-b2 status by FISH in cases scored 2+ immunohistochemically is strongly recommended.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
AIM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, Neoplasm,
http://linkedlifedata.com/resource/pubmed/chemical/DNA Topoisomerases, Type II,
http://linkedlifedata.com/resource/pubmed/chemical/DNA topoisomerase II alpha,
http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Tumor Markers, Biological
|
pubmed:status |
MEDLINE
|
pubmed:month |
Jul
|
pubmed:issn |
0002-9173
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
124
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
97-102
|
pubmed:dateRevised |
2010-11-18
|
pubmed:meshHeading |
pubmed-meshheading:15923160-Antigens, Neoplasm,
pubmed-meshheading:15923160-Breast Neoplasms,
pubmed-meshheading:15923160-DNA Topoisomerases, Type II,
pubmed-meshheading:15923160-DNA-Binding Proteins,
pubmed-meshheading:15923160-Female,
pubmed-meshheading:15923160-Gene Amplification,
pubmed-meshheading:15923160-Genes, erbB-2,
pubmed-meshheading:15923160-Humans,
pubmed-meshheading:15923160-Immunohistochemistry,
pubmed-meshheading:15923160-In Situ Hybridization, Fluorescence,
pubmed-meshheading:15923160-Neoplasm Metastasis,
pubmed-meshheading:15923160-Neoplasm Recurrence, Local,
pubmed-meshheading:15923160-Prognosis,
pubmed-meshheading:15923160-Sensitivity and Specificity,
pubmed-meshheading:15923160-Taiwan,
pubmed-meshheading:15923160-Tumor Markers, Biological
|
pubmed:year |
2005
|
pubmed:articleTitle |
erb-b2 amplification by fluorescence in situ hybridization in breast cancer specimens read as 2+ in immunohistochemical analysis.
|
pubmed:affiliation |
Division of Cancer Research, National Health Research Institutes, Taipei, Taiwan.
|
pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't
|