Metastatic Breast Cancer Survival according to HER2 and Topo2a Gene Status

The aim of this study was to determine the relationship between amplification of HER2 (Human epidermal growth factor receptor 2) and Topo2a (topoisomerase 2a) and their influence on prognosis in metastatic breast cancer (MBC) patients. Amplification of both HER2 and Topo2a genes was determined by ch...

Full description

Bibliographic Details
Main Authors: N. Todorović-Raković, Z. Nešković-Konstantinović, D. Nikolić-Vukosavljević
Format: Article
Language:English
Published: Hindawi Limited 2009-01-01
Series:Disease Markers
Online Access:http://dx.doi.org/10.3233/DMA-2009-0628
id doaj-538d1331610a4e31b1b2b665d6a987f4
record_format Article
spelling doaj-538d1331610a4e31b1b2b665d6a987f42020-11-25T00:20:40ZengHindawi LimitedDisease Markers0278-02401875-86302009-01-0126417118010.3233/DMA-2009-0628Metastatic Breast Cancer Survival according to HER2 and Topo2a Gene StatusN. Todorović-Raković0Z. Nešković-Konstantinović1D. Nikolić-Vukosavljević2Department of Experimental Oncology, Institute for Oncology and Radiology of Serbia, Belgrade, SerbiaDepartment of Clinical Oncology, Institute for Oncology and Radiology of Serbia, Belgrade, SerbiaDepartment of Experimental Oncology, Institute for Oncology and Radiology of Serbia, Belgrade, SerbiaThe aim of this study was to determine the relationship between amplification of HER2 (Human epidermal growth factor receptor 2) and Topo2a (topoisomerase 2a) and their influence on prognosis in metastatic breast cancer (MBC) patients. Amplification of both HER2 and Topo2a genes was determined by chromogenic in situ hybridization (CISH) in primary tumor tissue of 71 MBC patients. Starting point for follow-up was the time of diagnosis of metastatic disease. Although there was significant correlation between HER2 amplification and Topo2a alterations, Topo2a amplification was not strictly related to HER2 amplification. Follow-up of patients showed that there was no difference in MBC survival between HER2-nonamplified and HER2-amplified patients for subgroup as whole, but there was significant difference in MBC survival between patients with and without Topo2a amplification. HER2 amplification showed prognostic value in subgroups of patients, as well as Topo2a. Combination of these two genes with different status (nonamplified, amplified, coamplified) indicated that they might have additive effect. Also, it has been shown that Topo2a-amplified cases have poorer survival than Topo2a-nonamplified, when treated with CMF therapy.http://dx.doi.org/10.3233/DMA-2009-0628
collection DOAJ
language English
format Article
sources DOAJ
author N. Todorović-Raković
Z. Nešković-Konstantinović
D. Nikolić-Vukosavljević
spellingShingle N. Todorović-Raković
Z. Nešković-Konstantinović
D. Nikolić-Vukosavljević
Metastatic Breast Cancer Survival according to HER2 and Topo2a Gene Status
Disease Markers
author_facet N. Todorović-Raković
Z. Nešković-Konstantinović
D. Nikolić-Vukosavljević
author_sort N. Todorović-Raković
title Metastatic Breast Cancer Survival according to HER2 and Topo2a Gene Status
title_short Metastatic Breast Cancer Survival according to HER2 and Topo2a Gene Status
title_full Metastatic Breast Cancer Survival according to HER2 and Topo2a Gene Status
title_fullStr Metastatic Breast Cancer Survival according to HER2 and Topo2a Gene Status
title_full_unstemmed Metastatic Breast Cancer Survival according to HER2 and Topo2a Gene Status
title_sort metastatic breast cancer survival according to her2 and topo2a gene status
publisher Hindawi Limited
series Disease Markers
issn 0278-0240
1875-8630
publishDate 2009-01-01
description The aim of this study was to determine the relationship between amplification of HER2 (Human epidermal growth factor receptor 2) and Topo2a (topoisomerase 2a) and their influence on prognosis in metastatic breast cancer (MBC) patients. Amplification of both HER2 and Topo2a genes was determined by chromogenic in situ hybridization (CISH) in primary tumor tissue of 71 MBC patients. Starting point for follow-up was the time of diagnosis of metastatic disease. Although there was significant correlation between HER2 amplification and Topo2a alterations, Topo2a amplification was not strictly related to HER2 amplification. Follow-up of patients showed that there was no difference in MBC survival between HER2-nonamplified and HER2-amplified patients for subgroup as whole, but there was significant difference in MBC survival between patients with and without Topo2a amplification. HER2 amplification showed prognostic value in subgroups of patients, as well as Topo2a. Combination of these two genes with different status (nonamplified, amplified, coamplified) indicated that they might have additive effect. Also, it has been shown that Topo2a-amplified cases have poorer survival than Topo2a-nonamplified, when treated with CMF therapy.
url http://dx.doi.org/10.3233/DMA-2009-0628
work_keys_str_mv AT ntodorovicrakovic metastaticbreastcancersurvivalaccordingtoher2andtopo2agenestatus
AT zneskovickonstantinovic metastaticbreastcancersurvivalaccordingtoher2andtopo2agenestatus
AT dnikolicvukosavljevic metastaticbreastcancersurvivalaccordingtoher2andtopo2agenestatus
_version_ 1725365929783590912