Evidence map›Paper›PMID 40226589›Full record

ArticleFrontiers in cell and developmental biology2025

Increased amounts of cell-free DNA released from a culture with a high content of cancer stem cells.

Ileana J Fernández-Domínguez, Enrique Pérez-Cárdenas, Lucia Taja-Chayeb, Talia Wegman-Ostrosky, Claudia H S Caro-Sánchez, Alejandro Zentella-Dehesa, Alfonso Dueñas-González, Horacio López-Basabe, Rocío Morales-Bárcenas, Catalina Trejo-Becerril

Abstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Ileana J Fernández-DomínguezSubdirección de Investigación Básica, Instituto Nacional de Cancerología, México City, Mexico.
Enrique Pérez-CárdenasSubdirección de Investigación Básica, Instituto Nacional de Cancerología, México City, Mexico.
Lucia Taja-ChayebSubdirección de Investigación Básica, Instituto Nacional de Cancerología, México City, Mexico.
Talia Wegman-OstroskySubdirección de Investigación Básica, Instituto Nacional de Cancerología, México City, Mexico.
Claudia H S Caro-SánchezDepartamento de Patología del Instituto Nacional de Cancerología, México City, Mexico.
Alejandro Zentella-DehesaDepartamento de Medicina Genómica y Toxicología Ambiental, Instituto de Investigaciones Biomédicas (IIBO), Universidad Nacional Autónoma de México (UNAM), México City, Mexico.
Alfonso Dueñas-GonzálezSubdirección de Investigación Básica, Instituto Nacional de Cancerología, México City, Mexico.
Horacio López-BasabeDepartamento de Gastroenterología del Instituto Nacional de Cancerología, México City, Mexico.
Rocío Morales-BárcenasSubdirección de Investigación Básica, Instituto Nacional de Cancerología, México City, Mexico.
Catalina Trejo-BecerrilSubdirección de Investigación Básica, Instituto Nacional de Cancerología, México City, Mexico.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The study and characterization of cell-free DNA (cfDNA) has gained significant importance due to its clinical applications as a diagnostic and prognostic marker. However, it remains unclear whether all cell populations within a tumor or culture contribute equally to its release. This pioneering research analyzes the contribution of cancer stem cells (CSCs) in colon cancer cell lines to the amount of cfDNA released and its role in cellular transformation. Methods: The CSC population derived from the SW480 colon cancer cell line was enriched using a non-adhesive culture system to assess the quantity and electrophoretic profile of the released cfDNA. Subsequently, Results: Our study revealed that cultures with CSCs released greater amounts of cfDNA, displaying a distinct fragment profile. Additionally, cfDNA from different cellular origins influenced the transformation characteristics of NIH3T3 cells. This is the first demonstration of a link between CSC proportions and cfDNA release, suggesting that CSCs and microenvironmental conditions can affect cfDNA quantity and its potential to induce transformation. Conclusion: These findings highlight the importance of cfDNA in carcinogenesis and its potential as a biomarker and therapeutic target, especially given the role of CSCs in drug resistance and tumor aggressiveness.

Indexed as

3D culturecancer stem cellscell-free DNAcellular transformationcolorectal cancerhorizontal DNA transfer

Identifiers

PMID40226589
PMCPMC11985834

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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.