Evidence map›Paper›PMID 25471453›Full record

ArticleEMBO molecular medicine2014

eEF2K--a new target in breast cancers with combined inactivation of p53 and PTEN.

Hege G Russnes, Carlos Caldas

Open access · goldAbstract readComment
In one paragraph

Article in EMBO molecular medicine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.1field-weighted citation impact, top 45% 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

7 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. [The effect of miR-155 on HBV replication and PTEN expression in vivo].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2018
    Article
  7. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors at 2 institutions in 2 countries.

Hege G RussnesDepartment of Genetics, Institute for Cancer Research and Department of Pathology, Oslo University Hospital, Oslo, Norway K. G. Jebsen Center for Breast Cancer Research, University of Oslo, Oslo, Norway.
Carlos CaldasCancer Research UK Cambridge Institute and Department of Oncology, Li Ka Shing Centre, University of Cambridge, Cambridge, UK.
University of Cambridge · GBUniversity of Oslo · NO

Funding

Cancer Research UK 16942
6 · The paper itself

Abstract

Extensive efforts have now characterized the somatic molecular alterations in human breast cancer (Cancer Genome Atlas Network, 2012; Stephens et al, 2012) and have led to a re-definition of the disease as a constellation of 10 distinct driver-based subtypes (IntClust subtypes) (Curtis et al, 2012). The pursuit of druggable targets for each of these subtypes is now pressing. This is elegantly illustrated by the work of Liu et al (2014).

Indexed as

Gene DeletionAnimalsElongation Factor 2 KinaseFemaleHumansPTEN PhosphohydrolaseTriple Negative Breast NeoplasmsTumor Suppressor Protein p53Elongation Factor 2 KinasePTEN PhosphohydrolaseTumor Suppressor Protein p53

Identifiers

PMID25471453
PMCPMC4287969
OpenAlexW2117800505

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.