Evidence map›Paper›PMID 23285175›Full record

ArticlePloS one2012

Cancer progression mediated by horizontal gene transfer in an in vivo model.

Catalina Trejo-Becerril, Enrique Pérez-Cárdenas, Lucía Taja-Chayeb, Philippe Anker, Roberto Herrera-Goepfert, Luis A Medina-Velázquez, Alfredo Hidalgo-Miranda, Delia Pérez-Montiel, Alma Chávez-Blanco, Judith Cruz-Velázquez and 3 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 74 papers.

0numbers the graph read from it
0cells of the map it votes in
74citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

74 citing papers in PubMed, 130 citations in OpenAlex.

  1. Article
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  8. Review
  9. Predicting horizontal gene transfers with perfect transfer networks.Algorithms for molecular biology : AMB · 2024
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  18. Metastatic Melanoma: Liquid Biopsy as a New Precision Medicine Approach.International journal of molecular sciences · 2023
    Review
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  20. Review

14 more citing papers are in PubMed but not listed here.

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

13 authors at 4 institutions in 1 country.

Catalina Trejo-BecerrilDivision of Basic Research, Instituto Nacional de Cancerología, Mexico City, Mexico.
Enrique Pérez-Cárdenas
Lucía Taja-Chayeb
Philippe Anker
Roberto Herrera-Goepfert
Luis A Medina-Velázquez
Alfredo Hidalgo-Miranda
Delia Pérez-Montiel
Alma Chávez-Blanco
Judith Cruz-Velázquez
José Díaz-Chávez
Miguel Gaxiola
Alfonso Dueñas-González
Instituto Nacional de Cancerología · MXInstituto Nacional de Enfermedades Respiratorias · MXNational Institute of Genomic Medicine · MXUniversidad Nacional Autónoma de México · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It is known that cancer progresses by vertical gene transfer, but this paradigm ignores that DNA circulates in higher organisms and that it is biologically active upon its uptake by recipient cells. Here we confirm previous observations on the ability of cell-free DNA to induce in vitro cell transformation and tumorigenesis by treating NIH3T3 recipient murine cells with serum of colon cancer patients and supernatant of SW480 human cancer cells. Cell transformation and tumorigenesis of recipient cells did not occur if serum and supernatants were depleted of DNA. It is also demonstrated that horizontal cancer progression mediated by circulating DNA occurs via its uptake by recipient cells in an in vivo model where immunocompetent rats subjected to colon carcinogenesis with 1,2-dimethylhydrazine had increased rate of colonic tumors when injected in the dorsum with human SW480 colon carcinoma cells as a source of circulating oncogenic DNA, which could be offset by treating these animals with DNAse I and proteases. Though the contribution of biologically active molecules other than DNA for this phenomenon to occur cannot be ruled out, our results support the fact that cancer cells emit into the circulation biologically active DNA to foster tumor progression. Further exploration of the horizontal tumor progression phenomenon mediated by circulating DNA is clearly needed to determine whether its manipulation could have a role in cancer therapy.

Indexed as

Gene Transfer, HorizontalAnimalsBase SequenceCell Line, TumorCell Transformation, NeoplasticColonic NeoplasmsCulture Media, ConditionedDisease Models, AnimalFemaleGene DosageGenes, rasHumansMiceNIH 3T3 Cellsrab GTP-Binding ProteinsRatsCulture Media, ConditionedRAB30 protein, humanrab GTP-Binding Proteins

Identifiers

PMID23285175
PMCPMC3532306
OpenAlexW2116737208

What OpenQuestion holds

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LicenceCC BY
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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.