Evidence map›Paper›PMID 41051593›Full record

ArticleCellular oncology (Dordrecht, Netherlands)2025

Genomic diversity and BCL9L mutational status in circulating tumor cells predict overall survival in metastatic colorectal cancer.

Joao M Alves, Nuria Estévez-Gómez, Roberto Piñeiro, Laura Muinelo-Romay, Patricia Mondelo-Macía, Mercedes Salgado, Agueda Iglesias-Gómez, Laura Codesido-Prada, Astrid Diez-Martín, Joaquin Cubiella and 1 more

Abstract read
In one paragraph

Article in Cellular oncology (Dordrecht, Netherlands), 2025. 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
–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

1 citing paper in PubMed.

  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

11 authors.

Joao M Alves *CINBIO, Universidade de Vigo, Vigo, 36310, Spain. jalves@uvigo.gal.ORCID http://orcid.org/0000-0002-9599-5463
Nuria Estévez-Gómez *CINBIO, Universidade de Vigo, Vigo, 36310, Spain.ORCID http://orcid.org/0000-0002-7281-3137
Roberto PiñeiroTranslational Medical Oncology Group, Oncomet, Health Research Institute of Santiago de Compostela (IDIS), Santiago de Compostela, Spain.ORCID http://orcid.org/0000-0001-9479-139X
Laura Muinelo-RomayCentro de Investigación Biomédica en Red de Cáncer (CIBERONC), Madrid, Spain.ORCID http://orcid.org/0000-0002-7456-7531
Patricia Mondelo-MacíaLiquid Biopsy Analysis Unit, Translational Medical Oncology Group, Health Research Institute of Santiago de Compostela (IDIS), Santiago de Compostela, Spain.
Mercedes SalgadoDepartment of Oncology, Hospital Universitario de Ourense, Research Group in Gastrointestinal Oncology-Ourense, Ourense, Spain.
Agueda Iglesias-GómezDepartment of Gastroenterology Hospital Universitario de Ourense, Research Group in Gastrointestinal Oncology-Ourense, Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), Ourense, Spain.
Laura Codesido-PradaDepartment of Gastroenterology Hospital Universitario de Ourense, Research Group in Gastrointestinal Oncology-Ourense, Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), Ourense, Spain.
Astrid Diez-MartínDepartment of Gastroenterology Hospital Universitario de Ourense, Research Group in Gastrointestinal Oncology-Ourense, Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), Ourense, Spain.ORCID http://orcid.org/0000-0001-8822-2991
Joaquin CubiellaDepartment of Gastroenterology Hospital Universitario de Ourense, Research Group in Gastrointestinal Oncology-Ourense, Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), Ourense, Spain.ORCID http://orcid.org/0000-0002-9994-4831
David PosadaCINBIO, Universidade de Vigo, Vigo, 36310, Spain. dposada@uvigo.es.ORCID http://orcid.org/0000-0003-1407-3406

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMetastatic colorectal cancer (mCRC) remains a major cause of cancer-related mortality, but few noninvasive biomarkers exist to track disease progression or inform treatment strategies. Circulating tumor cells (CTCs) offer a minimally invasive source of tumor material, yet the prognostic significance of their genomic diversity remains unclear.

methodsWe conducted whole-exome sequencing of CTC pools from 29 mCRC patients to characterize their mutational landscape and assess associations with overall survival.

resultsOur analysis revealed substantial variation in mutational burden among patients, with all CTC pools harboring non-silent mutations in key CRC driver genes. Higher genomic diversity in CTC pools was significantly associated with reduced overall survival. Additionally, non-silent mutations in BCL9L emerged as a strong predictor of patient survival.

conclusionGenomic diversity and BCL9L mutational status in CTC pools emerged as strong predictors of survival in mCRC, underscoring the potential of CTC genomic profiling as a minimally invasive and clinically relevant prognostic tool in mCRC.

Indexed as

Colorectal NeoplasmsMutationNeoplastic Cells, CirculatingAdultAgedExome SequencingFemaleGenomicsHumansMaleMiddle AgedNeoplasm MetastasisPrognosisCirculating tumor cellsColorectal cancerIntratumor genomic heterogeneityLiquid biopsyPrecision medicine

Identifiers

PMID41051593
PMCPMC12698839

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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.