Evidence map›Paper›PMID 36593457›Full record

ArticleBMC cancer2023

Differential presence of exons (DPE): sequencing liquid biopsy by NGS. A new method for clustering colorectal Cancer patients.

David Rubio-Mangas, Mariano García-Arranz, Yaima Torres-Rodriguez, Miguel León-Arellano, Javier Suela, Damián García-Olmo

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.7field-weighted citation impact, top 25% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. 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

6 authors at 3 institutions in 1 country.

David Rubio-MangasGenómica y Medicina, NIMGenetics, Madrid, Spain. S. L, 28108, Madrid, Spain. drubio@nimgenetics.com.
Mariano García-ArranzNew Therapy Laboratory, Instituto de Investigación Sanitaria Fundación Jiménez Díaz, 28040, Madrid, Spain.
Yaima Torres-RodriguezGenómica y Medicina, NIMGenetics, Madrid, Spain. S. L, 28108, Madrid, Spain.
Miguel León-ArellanoDepartment of Surgery, Hospital Fundación Jiménez Díaz, 28040, Madrid, Spain.
Javier SuelaGenómica y Medicina, NIMGenetics, Madrid, Spain. S. L, 28108, Madrid, Spain. jsuela@nimgenetics.com.
Damián García-OlmoNew Therapy Laboratory, Instituto de Investigación Sanitaria Fundación Jiménez Díaz, 28040, Madrid, Spain. damian.garcia@uam.es.
Instituto de Medicina Genómica · ESUniversidad Autónoma de Madrid · ESHospital Universitario Fundación Jiménez Díaz · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Differential presence of exons (DPE) by next generation sequencing (NGS) is a method of interpretation of whole exome sequencing. This method has been proposed to design a predictive and diagnostic algorithm with clinical value in plasma from patients bearing colorectal cancer (CRC). The aim of the present study was to determine a common exonic signature to discriminate between different clinical pictures, such as non-metastatic, metastatic and non-disease (healthy), using a sustainable and novel technology in liquid biopsy.Through DPE analysis, we determined the differences in DNA exon levels circulating in plasma between patients bearing CRC vs. healthy, patients bearing CRC metastasis vs. non-metastatic and patients bearing CRC metastasis vs. healthy comparisons. We identified a set of 510 exons (469 up and 41 down) whose differential presence in plasma allowed us to group and classify between the three cohorts. Random forest classification (machine learning) was performed and an estimated out-of-bag (OOB) error rate of 35.9% was obtained and the predictive model had an accuracy of 75% with a confidence interval (CI) of 56.6-88.5.In conclusion, the DPE analysis allowed us to discriminate between different patho-physiological status such as metastatic, non-metastatic and healthy donors. In addition, this analysis allowed us to obtain very significant values with respect to previous published results, since we increased the number of samples in our study. These results suggest that circulating DNA in patient's plasma may be actively released by cells and may be involved in intercellular communication and, therefore, may play a pivotal role in malignant transformation (genometastasis).

Indexed as

Cell-Free Nucleic AcidsColorectal NeoplasmsBiomarkers, TumorExonsHigh-Throughput Nucleotide SequencingHumansLiquid BiopsyMutationBiomarkers, TumorCell-Free Nucleic AcidsCell-free DNAColorectal cancerDifferential presence of exonsDPEGenometastasisMetastasisNGSWhole-exome sequencing

Identifiers

PMID36593457
PMCPMC9808981
OpenAlexW4313475983

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Registered trials

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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.