Evidence map›Paper›PMID 17661082›Full record

ArticleJournal of cancer research and clinical oncology2008

Gene copy numbers of HER family in breast cancer.

Anna Zaczek, Marzena Wełnicka-Jaśkiewicz, Krzysztof Piotr Bielawski, Janusz Jaśkiewicz, Andrzej Badzio, Włodzimierz Olszewski, Piotr Rhone, Jacek Jassem

Open access · greenAbstract read
In one paragraph

Article in Journal of cancer research and clinical oncology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

11 citing papers in PubMed, 26 citations in OpenAlex.

  1. Breast cancers withOncology letters · 2017
    Article
  2. Article
  3. 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
  4. Article
  5. E3 ubiquitin ligases in ErbB receptor quantity control.Seminars in cell & developmental biology · 2010
    Review
  6. HER2 and chromosome 17 effect on patient outcome in the N9831 adjuvant trastuzumab trial.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2010
    Article
  7. Article
  8. An unusual loss of EGFR gene copy in glioblastoma multiforme in a child: a case report and analysis of a successfully derived HGG-02 cell line.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2010
    Article
  9. Article
  10. ERBB3/HER3 and ERBB2/HER2 duet in mammary development and breast cancer.Journal of mammary gland biology and neoplasia · 2008
    Review
  11. Article
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

8 authors at 2 institutions in 1 country.

Anna ZaczekDepartment of Oncology and Radiotherapy, Medical University of Gdańsk, Debinki 7, 80-211 Gdańsk, Poland. azaczek@amg.gda.pl
Marzena Wełnicka-Jaśkiewicz
Krzysztof Piotr Bielawski
Janusz Jaśkiewicz
Andrzej Badzio
Włodzimierz Olszewski
Piotr Rhone
Jacek Jassem
Gdańsk Medical University · PLThe Maria Sklodowska-Curie National Research Institute of Oncology · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimThe aim of the study was to analyze the occurrence of abnormal gene copy numbers of all HER oncogenes and to correlate these alterations to other clinicopathological variables in a consecutive series of 225 breast cancer patients.

methodsGene copy number of HER oncogenes was analyzed with double differential polymerase chain reaction (ddPCR). Statistical analysis was performed with a set of nonparametric tests.

resultsSixty-five percent of the tumors contained abnormal gene copy number of at least one HER oncogene. Alterations of at least two oncogenes were found in 31% of cases. The correlations between average gene copy numbers (AGCNs) of particular HER oncogenes were much stronger in node positive compared to node-negative tumors. Deletions of EGFR were associated with the lack of steroid hormone receptors. The HER3 and HER4 amplifications were more common in well differentiated tumors.

conclusionsOur results indicate a key role of HER heterodimers in tumor progression and confirm earlier data that HER2 is the preferred partner for other HER oncogenes in this process. Deletions of EGFR were associated with unfavorable characteristics, whereas HER3 and HER4 amplifications may be linked with less aggressive phenotypes.

Indexed as

Gene DosageAdultAgedAged, 80 and overAntineoplastic Combined Chemotherapy ProtocolsBreast NeoplasmsCarcinoma, Ductal, BreastCarcinoma, LobularChemotherapy, AdjuvantDimerizationDNA, NeoplasmErbB ReceptorsFemaleGene AmplificationGenes, erbB-2HumansDNA, NeoplasmERBB4 protein, humanErbB ReceptorsReceptor, ErbB-3Receptor, ErbB-4

Identifiers

PMID17661082
PMCPMC12161684
OpenAlexW2016156577

What OpenQuestion holds

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Registered trials

None linked

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.