Evidence map›Paper›PMID 22871798›Full record

ArticleThe oncologist2012

Prognostic significance of TOP2A gene dosage in HER-2-negative breast cancer.

Anna J Zaczek, Aleksandra Markiewicz, Barbara Seroczynska, Jaroslaw Skokowski, Janusz Jaskiewicz, Tadeusz Pienkowski, Wojciech P Olszewski, Jolanta Szade, Piotr Rhone, Marzena Welnicka-Jaskiewicz and 1 more

Open access · hybridAbstract read
In one paragraph

Article in The oncologist, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.5field-weighted citation impact, top 17% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 24 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Article
  5. Clinical and Biological Significance ofInternational journal of molecular sciences · 2019
    Article
  6. Article
  7. Over-expression of TOP2A as a prognostic biomarker in patients with glioma.International journal of clinical and experimental pathology · 2018
    Article
  8. Article
  9. Clinical significance of topoisomerase 2A expression and gene change in operable invasive breast cancer.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2015
    Article
  10. BCL2 is an independent predictor of outcome in basal-like triple-negative breast cancers treated with adjuvant anthracycline-based chemotherapy.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2015
    Article
  11. Article
  12. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 4 institutions in 1 country.

Anna J ZaczekLaboratory of Cell Biology, Department of Medical Biotechnology, Intercollegiate Faculty of Biotechnology, University of Gdańsk and Medical University of Gdańsk, Dêbinki 1, 80-211 Gdańsk, Poland. azaczek@gumed.edu.pl
Aleksandra Markiewicz
Barbara Seroczynska
Jaroslaw Skokowski
Janusz Jaskiewicz
Tadeusz Pienkowski
Wojciech P Olszewski
Jolanta Szade
Piotr Rhone
Marzena Welnicka-Jaskiewicz
Jacek Jassem
Gdańsk Medical University · PLThe Maria Sklodowska-Curie National Research Institute of Oncology · PLMedical University of Warsaw · PLUniversity of Bydgoszcz · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPrevious studies showed the prognostic and predictive impact of human epidermal growth factor receptor 2 (HER-2) gene alterations analyzed separately and jointly with topoisomerase II α (TOP2A) gene alterations; however, the role of TOP2A gene abnormalities alone has not been thoroughly investigated. Additionally, TOP2A aberrations were typically studied in HER-2-positive (HER-2(+)) tumors because these genes are frequently coamplified. Therefore, the knowledge concerning the impact of TOP2A abnormalities in HER-2-negative (HER-2(-)) patients is scarce. This study aimed to investigate the clinical significance of TOP2A anomalies in breast cancer patients with HER-2(-) and HER-2(+) tumors. MATERIALS AND

methodsSnap-frozen tumor samples from 322 consecutive stage I-III breast cancer patients were analyzed for TOP2A gene dosage using quantitative real-time PCR (qPCR).

resultsA high TOP2A gene dosage was found in 94 tumors (29%)-32% and 27% of HER-2(+) and HER-2(-) tumors, respectively. The mean TOP2A gene dosages in the HER-2(+) and HER-2(-) groups were 1.49 ± 1.03 and 1.09 ± 0.35, respectively. High TOP2A gene dosage had an inverse prognostic impact in terms of shorter disease-free survival (DFS) and overall survival (OS) times in the entire group and in both the HER-2(-) and HER-2(+) subgroups. The unfavorable prognostic impact of TOP2A gene dosage was maintained in the multivariate Cox regression analysis in the entire group and in HER-2(-) patients.

conclusionsA high gene dosage of TOP2A determined using qPCR occurs frequently both in HER-2(+) and HER-2(-) tumors and has a strong adverse prognostic impact.

Indexed as

Gene DosageAgedAntigens, NeoplasmBreast NeoplasmsCell Line, TumorDNA-Binding ProteinsDNA Topoisomerases, Type IIErb-b2 Receptor Tyrosine KinasesFemaleHumansImmunohistochemistryIn Situ Hybridization, FluorescenceMiddle AgedNeoplasm StagingPoly-ADP-Ribose Binding ProteinsPrognosisAntigens, NeoplasmDNA-Binding ProteinsDNA Topoisomerases, Type IIErb-b2 Receptor Tyrosine KinasesPoly-ADP-Ribose Binding ProteinsTOP2A protein, human

Identifiers

PMID22871798
PMCPMC3481890
OpenAlexW2171839753

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.