Evidence map›Paper›PMID 26356674›Full record

ReviewOncotarget2015

The search for cis-regulatory driver mutations in cancer genomes.

Rebecca C Poulos, Mathew A Sloane, Luke B Hesson, Jason W H Wong

Open access · diamondAbstract readReview
In one paragraph

Review in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 21% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 24 citations in OpenAlex.

  1. On the Origin of Biomolecular Networks.Frontiers in genetics · 2019
    Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
  6. regCNN: identifyingComputational and structural biotechnology journal · 2022
    Article
  7. Article
  8. Review
  9. iScience · 2021
    Article
  10. Article
  11. Article
  12. Review
  13. 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

4 authors at 1 institution in 1 country.

Rebecca C PoulosPrince of Wales Clinical School and Lowy Cancer Research Centre, UNSW Australia, Sydney, Australia.
Mathew A SloanePrince of Wales Clinical School and Lowy Cancer Research Centre, UNSW Australia, Sydney, Australia.
Luke B HessonPrince of Wales Clinical School and Lowy Cancer Research Centre, UNSW Australia, Sydney, Australia.
Jason W H WongPrince of Wales Clinical School and Lowy Cancer Research Centre, UNSW Australia, Sydney, Australia.
UNSW Sydney · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

With the advent of high-throughput and relatively inexpensive whole-genome sequencing technology, the focus of cancer research has begun to shift toward analyses of somatic mutations in non-coding cis-regulatory elements of the cancer genome. Cis-regulatory elements play an important role in gene regulation, with mutations in these elements potentially resulting in changes to the expression of linked genes. The recent discoveries of recurrent TERT promoter mutations in melanoma, and recurrent mutations that create a super-enhancer regulating TAL1 expression in T-cell acute lymphoblastic leukaemia (T-ALL), have sparked significant interest in the search for other somatic cis-regulatory mutations driving cancer development. In this review, we look more closely at the TERT promoter and TAL1 enhancer alterations and use these examples to ask whether other cis-regulatory mutations may play a role in cancer susceptibility. In doing so, we make observations from the data emerging from recent research in this field, and describe the experimental and analytical approaches which could be adopted in the hope of better uncovering the true functional significance of somatic cis-regulatory mutations in cancer.

Indexed as

Genome, HumanMutationRegulatory Sequences, Nucleic AcidAnimalsBiomarkers, TumorDNA Mutational AnalysisGene Expression Regulation, NeoplasticGenetic Predisposition to DiseaseHigh-Throughput Nucleotide SequencingHumansNeoplasmsPhenotypeBiomarkers, Tumorcancercis-regulationenhancerpromotersomatic mutation

Identifiers

PMID26356674
PMCPMC4741709
OpenAlexW2195011736

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.