Evidence map›Paper›PMID 24156016›Full record

ArticleCancer medicine2013

High expression of ZNF703 independent of amplification indicates worse prognosis in patients with luminal B breast cancer.

Inga Reynisdottir, Adalgeir Arason, Berglind O Einarsdottir, Haukur Gunnarsson, Johan Staaf, Johan Vallon-Christersson, Goran Jonsson, Markus Ringnér, Bjarni A Agnarsson, Kristrun Olafsdottir and 7 more

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

25 citing papers in PubMed, 50 citations in OpenAlex.

  1. Phase II Study of AZD4547 in Patients With Tumors Harboring Aberrations in the FGFR Pathway: Results From the NCI-MATCH Trial (EAY131) Subprotocol W.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2020
    Trial
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  5. Pharmaceutics · 2023
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  18. Proceedings of the National Academy of Sciences of the United States of America · 2017
    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

17 authors at 5 institutions in 3 countries.

Inga ReynisdottirDepartment of Pathology, Landspitali-University Hospital 101, Reykjavik, Iceland.
Adalgeir Arason
Berglind O Einarsdottir
Haukur Gunnarsson
Johan Staaf
Johan Vallon-Christersson
Goran Jonsson
Markus Ringnér
Bjarni A Agnarsson
Kristrun Olafsdottir
Rainer Fagerholm
Thorbjorg Einarsdottir
Gudrun Johannesdottir
Oskar Thor Johannsson
Heli Nevanlinna
Ake Borg
Rosa Bjork Barkardottir
Lund University · SENational University Hospital of Iceland · ISReykjavík University · ISHelsinki University Hospital · FIUniversity of Helsinki · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Amplification of 8p12-p11 is relatively common in breast cancer and several genes within the region have been suggested to affect breast tumor progression. The aim of the study was to map the amplified 8p12-p11 region in a large set of breast tumors in an effort to identify the genetic driver and to explore its impact on tumor progression and prognosis. Copy number alterations (CNAs) were mapped in 359 tumors, and gene expression data from 577 tumors (359 tumors included) were correlated with CNA, clinical-pathological factors, and protein expression (39 tumors). 8p12-p11 was amplified in 11.4% of tumors. The smallest region of amplification harbored one full-length gene, ZNF703. ZNF703 mRNA expression was significantly higher in estrogen receptor (ER)-positive than ER-negative tumors (P = 2 × 10(-16)), a reflection of high expression in luminal tumors. Forty-eight percent of tumors with ZNF703 amplification were luminal B tumors in which the best correlation between DNA copy number and mRNA was seen (P = 1.2 × 10(-7)) as well as correlation between mRNA and protein expression (P = 0.02). High ZNF703 mRNA correlated with poor survival in patients with ER-positive luminal B tumors (log rank P = 0.04). Furthermore, high ZNF703 mRNA expression correlated with poor outcome in patients with ZNF703 copy number neutral, ER-positive, luminal B tumors (log rank P = 0.004). The results support ZNF703 as the driver gene of the 8p12 amplification and suggest that independent of amplification, high expression of the gene affects prognosis in luminal B tumors.

Indexed as

Gene AmplificationGene ExpressionAdultAgedAged, 80 and overBreast NeoplasmsCarrier ProteinsChromosome MappingChromosomes, Human, Pair 8FemaleGene Expression ProfilingHumansMiddle AgedNeoplasm GradingPrognosisRNA, MessengerCarrier ProteinsRNA, MessengerZNF703 protein, human8p12-p11 amplificationER positiveluminal tumorsprognosistumor progressionZNF703

Identifiers

PMID24156016
PMCPMC3799278
OpenAlexW2109424608

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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.