Evidence map›Paper›PMID 31790386›Full record

ArticlePLoS computational biology2019

CBNA: A control theory based method for identifying coding and non-coding cancer drivers.

Vu V H Pham, Lin Liu, Cameron P Bracken, Gregory J Goodall, Qi Long, Jiuyong Li, Thuc D Le

Abstract read
In one paragraph

Article in PLoS computational biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. 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

7 authors.

Vu V H PhamSchool of Information Technology and Mathematical Sciences, University of South Australia, Mawson Lakes, Australia.ORCID 0000-0002-8884-3584
Lin LiuSchool of Information Technology and Mathematical Sciences, University of South Australia, Mawson Lakes, Australia.
Cameron P BrackenCentre for Cancer Biology, an alliance of SA Pathology and University of South Australia, Adelaide, Australia.
Gregory J GoodallCentre for Cancer Biology, an alliance of SA Pathology and University of South Australia, Adelaide, Australia.ORCID 0000-0003-1294-0692
Qi LongPerelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America.
Jiuyong LiSchool of Information Technology and Mathematical Sciences, University of South Australia, Mawson Lakes, Australia.ORCID 0000-0002-9023-1878
Thuc D LeSchool of Information Technology and Mathematical Sciences, University of South Australia, Mawson Lakes, Australia.ORCID 0000-0002-9732-4313

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A key task in cancer genomics research is to identify cancer driver genes. As these genes initialise and progress cancer, understanding them is critical in designing effective cancer interventions. Although there are several methods developed to discover cancer drivers, most of them only identify coding drivers. However, non-coding RNAs can regulate driver mutations to develop cancer. Hence, novel methods are required to reveal both coding and non-coding cancer drivers. In this paper, we develop a novel framework named Controllability based Biological Network Analysis (CBNA) to uncover coding and non-coding cancer drivers (i.e. miRNA cancer drivers). CBNA integrates different genomic data types, including gene expression, gene network, mutation data, and contains a two-stage process: (1) Building a network for a condition (e.g. cancer condition) and (2) Identifying drivers. The application of CBNA to the BRCA dataset demonstrates that it is more effective than the existing methods in detecting coding cancer drivers. In addition, CBNA also predicts 17 miRNA drivers for breast cancer. Some of these predicted miRNA drivers have been validated by literature and the rest can be good candidates for wet-lab validation. We further use CBNA to detect subtype-specific cancer drivers and several predicted drivers have been confirmed to be related to breast cancer subtypes. Another application of CBNA is to discover epithelial-mesenchymal transition (EMT) drivers. Of the predicted EMT drivers, 7 coding and 6 miRNA drivers are in the known EMT gene lists.

Indexed as

OncogenesBreast NeoplasmsComputational BiologyDatabases, GeneticEpithelial-Mesenchymal TransitionFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticGene Regulatory NetworksHumansMicroRNAsModels, GeneticMutationNeoplasmsRNA, MessengerRNA, NeoplasmMicroRNAsRNA, MessengerRNA, NeoplasmRNA, UntranslatedTranscription Factors

Identifiers

PMID31790386
PMCPMC6907873

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.