Evidence map›Paper›PMID 25335079›Full record

ArticlePloS one2014

Integrated exon level expression analysis of driver genes explain their role in colorectal cancer.

Mohammad Azhar Aziz, Sathish Periyasamy, Zeyad Al Yousef, Ibrahim AlAbdulkarim, Majed Al Otaibi, Abdulaziz Alfahed, Glowi Alasiri

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

19 citing papers in PubMed, 26 citations in OpenAlex.

  1. Trial
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  7. Alternatively Spliced Isoforms ofJournal of personalized medicine · 2023
    Article
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  12. Multi-omics Integration Analysis Robustly Predicts High-Grade Patient Survival and Identifies CPT1B Effect on Fatty Acid Metabolism in Bladder Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2019
    Article
  13. Article
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  16. Long non-coding RNA LINC01296 is a potential prognostic biomarker in patients with colorectal cancer.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2015
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Mohammad Azhar AzizMedical Genomics, King Abdullah International Medical Research Center, Riyadh, Saudi Arabia.
Sathish PeriyasamyBioinformatics, King Abdullah International Medical Research Center, Riyadh, Saudi Arabia.
Zeyad Al YousefSurgery, National Guard Health Affairs, Riyadh, Saudi Arabia.
Ibrahim AlAbdulkarimMedical Genomics, King Abdullah International Medical Research Center, Riyadh, Saudi Arabia.
Majed Al OtaibiMedical Genomics, King Abdullah International Medical Research Center, Riyadh, Saudi Arabia.
Abdulaziz AlfahedMedical Genomics, King Abdullah International Medical Research Center, Riyadh, Saudi Arabia.
Glowi AlasiriMedical Genomics, King Abdullah International Medical Research Center, Riyadh, Saudi Arabia.
King Abdullah International Medical Research Center · SANational Guard Health Affairs · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Integrated analysis of genomic and transcriptomic level changes holds promise for a better understanding of colorectal cancer (CRC) biology. There is a pertinent need to explain the functional effect of genome level changes by integrating the information at the transcript level. Using high resolution cytogenetics array, we had earlier identified driver genes by 'Genomic Identification of Significant Targets In Cancer (GISTIC)' analysis of paired tumour-normal samples from colorectal cancer patients. In this study, we analyze these driver genes at three levels using exon array data--gene, exon and network. Gene level analysis revealed a small subset to experience differential expression. These results were reinforced by carrying out separate differential expression analyses (SAM and LIMMA). ATP8B1 was found to be the novel gene associated with CRC that shows changes at cytogenetic, gene and exon levels. Splice index of 29 exons corresponding to 13 genes was found to be significantly altered in tumour samples. Driver genes were used to construct regulatory networks for tumour and normal groups. There were rearrangements in transcription factor genes suggesting the presence of regulatory switching. The regulatory pattern of AHR gene was found to have the most significant alteration. Our results integrate data with focus on driver genes resulting in highly enriched novel molecules that need further studies to establish their role in CRC.

Indexed as

Adenosine TriphosphatasesAlternative SplicingBiomarkersColorectal NeoplasmsCytogenetic AnalysisExonsGene Expression Regulation, NeoplasticGene Regulatory NetworksHumansOligonucleotide Array Sequence AnalysisPrincipal Component AnalysisAdenosine TriphosphatasesATP8B1 protein, humanBiomarkers

Identifiers

PMID25335079
PMCPMC4204855
OpenAlexW2048351097

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.