Evidence map›Paper›PMID 28854983›Full record

ArticleGenome medicine2017

Identification of cis-regulatory mutations generating de novo edges in personalized cancer gene regulatory networks.

Zeynep Kalender Atak, Hana Imrichova, Dmitry Svetlichnyy, Gert Hulselmans, Valerie Christiaens, Joke Reumers, Hugo Ceulemans, Stein Aerts

Abstract read
In one paragraph

Article in Genome medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
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

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. iScience · 2021
    Article
  6. Open medicine (Warsaw, Poland) · 2021
    Article
  7. Review
  8. Article
  9. lncRNA MEG3 inhibits the growth of hepatocellular carcinoma cells by sponging miR-9-5p to upregulate SOX11.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2019
    Article
  10. Review
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.

Zeynep Kalender AtakLaboratory of Computational Biology, VIB Center for Brain & Disease Research, Leuven, Belgium.
Hana ImrichovaLaboratory of Computational Biology, VIB Center for Brain & Disease Research, Leuven, Belgium.
Dmitry SvetlichnyyLaboratory of Computational Biology, VIB Center for Brain & Disease Research, Leuven, Belgium.
Gert HulselmansLaboratory of Computational Biology, VIB Center for Brain & Disease Research, Leuven, Belgium.
Valerie ChristiaensLaboratory of Computational Biology, VIB Center for Brain & Disease Research, Leuven, Belgium.
Joke ReumersDiscovery Sciences, Janssen Research & Development, Turnhoutseweg 30, 2340, Beerse, Belgium.
Hugo CeulemansDiscovery Sciences, Janssen Research & Development, Turnhoutseweg 30, 2340, Beerse, Belgium.
Stein AertsLaboratory of Computational Biology, VIB Center for Brain & Disease Research, Leuven, Belgium. stein.aerts@kuleuven.be.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The identification of functional non-coding mutations is a key challenge in the field of genomics. Here we introduce μ-cisTarget to filter, annotate and prioritize cis-regulatory mutations based on their putative effect on the underlying "personal" gene regulatory network. We validated μ-cisTarget by re-analyzing the TAL1 and LMO1 enhancer mutations in T-ALL, and the TERT promoter mutation in melanoma. Next, we re-sequenced the full genomes of ten cancer cell lines and used matched transcriptome data and motif discovery to identify master regulators with de novo binding sites that result in the up-regulation of nearby oncogenic drivers. μ-cisTarget is available from http://mucistarget.aertslab.org .

Indexed as

Gene Regulatory NetworksGenes, NeoplasmMutationRegulatory Sequences, Nucleic AcidAlgorithmsBinding SitesCell Line, TumorDNA Mutational AnalysisFemaleGene Expression ProfilingGenomicsHumansMaleNeoplasmsPrecision MedicineTranscription FactorsTranscription FactorsCancer genomicscis-regulatory mutationsGene regulatory networksWhole-genome sequencing

Identifiers

PMID28854983
PMCPMC5575942

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.