Evidence map›Paper›PMID 27669316›Full record

ArticleMicroarrays (Basel, Switzerland)2016

OSAnalyzer: A Bioinformatics Tool for the Analysis of Gene Polymorphisms Enriched with Clinical Outcomes.

Giuseppe Agapito, Cirino Botta, Pietro Hiram Guzzi, Mariamena Arbitrio, Maria Teresa Di Martino, Pierfrancesco Tassone, Pierosandro Tagliaferri, Mario Cannataro

Abstract read
In one paragraph

Article in Microarrays (Basel, Switzerland), 2016. 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
–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

4 citing papers in PubMed.

  1. Article
  2. DMETHigh-throughput · 2020
    Review
  3. Article
  4. 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

8 authors.

Giuseppe AgapitoDepartment of Medical and Surgical Science, University Magna Graecia of Catanzaro, Catanzaro 88100, Italy. agapito@unicz.it.
Cirino BottaDepartment of Experimental Medicine and Clinic, University Magna Graecia of Catanzaro, Catanzaro 88100, Italy. cirino.botta@gmail.com.
Pietro Hiram GuzziDepartment of Medical and Surgical Science, University Magna Graecia of Catanzaro, Catanzaro 88100, Italy. hguzzi@unicz.it.
Mariamena ArbitrioISN-CNR, Roccelletta di Borgia, Catanzaro 88100, Italy. mariamena.arbitrio@cnr.it.
Maria Teresa Di MartinoDepartment of Experimental Medicine and Clinic, University Magna Graecia of Catanzaro, Catanzaro 88100, Italy. teresadm@unicz.it.
Pierfrancesco TassoneDepartment of Experimental Medicine and Clinic, University Magna Graecia of Catanzaro, Catanzaro 88100, Italy. tassone@unicz.it.
Pierosandro TagliaferriDepartment of Experimental Medicine and Clinic, University Magna Graecia of Catanzaro, Catanzaro 88100, Italy. tagliaferri@unicz.it.
Mario CannataroDepartment of Medical and Surgical Science, University Magna Graecia of Catanzaro, Catanzaro 88100, Italy. cannataro@unicz.it.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe identification of biomarkers for the estimation of cancer patients' survival is a crucial problem in modern oncology. Recently, the Affymetrix DMET (Drug Metabolizing Enzymes and Transporters) microarray platform has offered the possibility to determine the ADME (absorption, distribution, metabolism, and excretion) gene variants of a patient and to correlate them with drug-dependent adverse events. Therefore, the analysis of survival distribution of patients starting from their profile obtained using DMET data may reveal important information to clinicians about possible correlations among drug response, survival rate, and gene variants.

methodsIn order to provide support to this analysis we developed OSAnalyzer, a software tool able to compute the overall survival (OS) and progression-free survival (PFS) of cancer patients and evaluate their association with ADME gene variants.

resultsThe tool is able to perform an automatic analysis of DMET data enriched with survival events. Moreover, results are ranked according to statistical significance obtained by comparing the area under the curves that is computed by using the log-rank test, allowing a quick and easy analysis and visualization of high-throughput data.

conclusionsFinally, we present a case study to highlight the usefulness of OSAnalyzer when analyzing a large cohort of patients.

Indexed as

ADME genesgenotyping microarraysoverall survivalpharmacogenomicsprogression-free survival

Identifiers

PMID27669316
PMCPMC5197943

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