rdf:type |
|
lifeskim:mentions |
umls-concept:C0005516,
umls-concept:C0006142,
umls-concept:C0013216,
umls-concept:C0205225,
umls-concept:C0256022,
umls-concept:C0449438,
umls-concept:C0600558,
umls-concept:C0681890,
umls-concept:C0871261,
umls-concept:C1537647,
umls-concept:C1704632,
umls-concept:C1706817,
umls-concept:C2911692
|
pubmed:issue |
3
|
pubmed:dateCreated |
2010-3-1
|
pubmed:abstractText |
This study aimed at evaluating the usefulness of topoisomerase II alpha (TOP2A) for predicting the effect of anthracycline-based neoadjuvant chemotherapy in breast cancer. The TOP2A status was examined using fluorescent in situ hybridization (FISH) in 14 pre-chemotherapeutic breast cancer tissues, and was also assessed by immunohistochemistry (IHC) in 14 pairs of pre- and post-chemotherapeutic breast cancer specimens. TOP2A gene aberration by IHC tended to show a correlation with pathological responses but this was not statistically significant (p=0.060). On the other hand, the low TOP2A/CEP17 ratio correlated with good pathological responses (p=0.012). TOP2A overexpression was not significantly associated with response (p=0.580). Our results thus suggest that the TOP2A/CEP17 ratio may be a useful predictor of the effects of anthracycline-based neoadjuvant chemotherapy in breast cancer.
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:month |
Mar
|
pubmed:issn |
1618-0631
|
pubmed:author |
pubmed-author:AokiIchiroI,
pubmed-author:IshikawaTakashiT,
pubmed-author:KawachiKaeK,
pubmed-author:KitoAyakoA,
pubmed-author:MachinamiRikuoR,
pubmed-author:MurakamiAyumiA,
pubmed-author:NagashimaYojiY,
pubmed-author:NozawaAkinoriA,
pubmed-author:OtaIkukoI,
pubmed-author:SasakiTakeshiT,
pubmed-author:ShimizuDaisukeD
|
pubmed:copyrightInfo |
Copyright 2009 Elsevier GmbH. All rights reserved.
|
pubmed:issnType |
Electronic
|
pubmed:day |
15
|
pubmed:volume |
206
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
156-62
|
pubmed:dateRevised |
2010-11-18
|
pubmed:meshHeading |
pubmed-meshheading:20089371-Adult,
pubmed-meshheading:20089371-Aged,
pubmed-meshheading:20089371-Anthracyclines,
pubmed-meshheading:20089371-Antigens, Neoplasm,
pubmed-meshheading:20089371-Antineoplastic Agents,
pubmed-meshheading:20089371-Breast Neoplasms,
pubmed-meshheading:20089371-DNA Topoisomerases, Type II,
pubmed-meshheading:20089371-DNA-Binding Proteins,
pubmed-meshheading:20089371-Drug Resistance, Neoplasm,
pubmed-meshheading:20089371-Female,
pubmed-meshheading:20089371-Humans,
pubmed-meshheading:20089371-Immunohistochemistry,
pubmed-meshheading:20089371-In Situ Hybridization, Fluorescence,
pubmed-meshheading:20089371-Middle Aged,
pubmed-meshheading:20089371-Neoadjuvant Therapy,
pubmed-meshheading:20089371-Tumor Markers, Biological
|
pubmed:year |
2010
|
pubmed:articleTitle |
The topoisomerase II alpha gene status in primary breast cancer is a predictive marker of the response to anthracycline-based neoadjuvant chemotherapy.
|
pubmed:affiliation |
Division of Anatomic and Surgical Pathology, Yokohama City University Medical Center, Minami-ku, Yokohama, Japan. kw1151@urahp.yokohama-cu.ac.jp
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|