Evidence map›Paper›PMID 25622824›Full record

ArticleScientific reports2015

Systems approach for the selection of micro-RNAs as therapeutic biomarkers of anti-EGFR monoclonal antibody treatment in colorectal cancer.

Avisek Deyati, Shweta Bagewadi, Philipp Senger, Martin Hofmann-Apitius, Natalia Novac

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 36% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Personalized medicine in colorectal cancer.Gastroenterology and hepatology from bed to bench · 2020
    Review
  2. Article
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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

5 authors at 3 institutions in 1 country.

Avisek Deyati1] Fraunhofer Institute SCAI, Schloss Birlinghoven, 53754 Sankt Augustin, Germany [2] Bonn-Aachen International Center for Information Technology (B-IT), Department of Applied Life Science Informatics, 53113 Bonn, Germany.
Shweta Bagewadi1] Fraunhofer Institute SCAI, Schloss Birlinghoven, 53754 Sankt Augustin, Germany [2] Bonn-Aachen International Center for Information Technology (B-IT), Department of Applied Life Science Informatics, 53113 Bonn, Germany.
Philipp Senger1] Fraunhofer Institute SCAI, Schloss Birlinghoven, 53754 Sankt Augustin, Germany [2] Bonn-Aachen International Center for Information Technology (B-IT), Department of Applied Life Science Informatics, 53113 Bonn, Germany.
Martin Hofmann-Apitius1] Fraunhofer Institute SCAI, Schloss Birlinghoven, 53754 Sankt Augustin, Germany [2] Bonn-Aachen International Center for Information Technology (B-IT), Department of Applied Life Science Informatics, 53113 Bonn, Germany.
Natalia NovacMerck Serono, Frankfurter Strasse 250, 64293 Darmstadt, Germany.
Bonn Aachen International Center for Information Technology · DEFraunhofer Institute for Algorithms and Scientific Computing · DEMerck (Germany) · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

miRNA plays an important role in tumourgenesis by regulating expression of oncogenes and tumour suppressors. Thus affects cell proliferation and differentiation, apoptosis, invasion and angiogenesis. miRNAs are potential biomarkers for diagnosis, prognosis and therapies of different forms of cancer. However, relationship between response of cancer patients towards targeted therapy and the resulting modifications of the miRNA transcriptome in the context of pathway regulation is poorly understood. With ever-increasing pathways and miRNA-mRNA interaction databases, freely available mRNA and miRNA expression data in multiple cancer therapy have produced an unprecedented opportunity to decipher the role of miRNAs in early prediction of therapeutic efficacy in diseases. Efficient translation of -omics data and accumulated knowledge to clinical decision-making are of paramount scientific and public health interest. Well-structured translational algorithms are needed to bridge the gap from databases to decisions. Herein, we present a novel SMARTmiR algorithm to prospectively predict the role of miRNA as therapeutic biomarker for an anti-EGFR monoclonal antibody i.e. cetuximab treatment in colorectal cancer.

Indexed as

AlgorithmsAntibodies, MonoclonalApoptosisBiomarkers, TumorCell DifferentiationCell MovementCell ProliferationCetuximabColorectal NeoplasmsErbB ReceptorsGene Expression Regulation, NeoplasticHumansMicroRNAsAntibodies, MonoclonalBiomarkers, TumorCetuximabErbB ReceptorsMicroRNAs

Identifiers

PMID25622824
PMCPMC5389028
OpenAlexW2024376725

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.