Evidence map›Paper›PMID 41530861›Full record

ReviewJournal of experimental & clinical cancer research : CR2026

Reconstructing the metastatic journey: functional circulating tumor cells and disseminated tumor cells based models for translational oncology.

Caroline Sanglier, Laure Cayrefourcq, Catherine Alix-Panabières

Abstract readReview
In one paragraph

Review in Journal of experimental & clinical cancer research : CR, 2026. 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. Review
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

3 authors.

Caroline SanglierLaboratory of Rare Human Circulating Cells (LCCRH), University Medical Centre of Montpellier, Site Unique de Biologie (SUB), 371, Avenue du Doyen Gaston Giraud, 34295 Cedex 5, Montpellier, France.
Laure CayrefourcqLaboratory of Rare Human Circulating Cells (LCCRH), University Medical Centre of Montpellier, Site Unique de Biologie (SUB), 371, Avenue du Doyen Gaston Giraud, 34295 Cedex 5, Montpellier, France.
Catherine Alix-PanabièresLaboratory of Rare Human Circulating Cells (LCCRH), University Medical Centre of Montpellier, Site Unique de Biologie (SUB), 371, Avenue du Doyen Gaston Giraud, 34295 Cedex 5, Montpellier, France. c-panabieres@chu-montpellier.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metastatic progression, driven by the dissemination of circulating tumor cells (CTCs) through the bloodstream, remains the leading cause of cancer-related death. A rare subset of CTCs, characterized by tumor-initiating properties and phenotypic plasticity, plays a pivotal role in the formation of distant metastases. The ability of these cells to survive in the circulation, evade the immune surveillance, and establish secondary tumors underscores their biological significance. However, CTC extreme rarity and heterogeneity pose major challenges for their in-depth functional characterization. Disseminated tumor cells (DTCs) are cells that have extravasated and persist in distant organ niches, often in a dormant state, and represent a complementary and equally critical component of metastatic progression. Their capacity to remain quiescent for prolonged periods before reactivation highlights the need to study both CTCs and DTCs to fully understand metastasis initiation and relapse. Recent advances in CTC isolation and culture have led to the development of patient-derived CTC lines and CTC-derived xenograft animal models, offering unprecedented opportunities to investigate metastatic seeding, therapeutic resistance and tumor evolution. CTC- and DTC-based models provide valuable insights into the biology of CTCs from different cancer types, revealing key molecular drivers of metastasis formation and potential therapeutic targets. In this review, we summarize the state-of-the-art methodologies for establishing CTC- and DTC-based models and evaluate their contribution to understand tumor progression and response to treatments. We discuss the current challenges in generating and maintaining these models, including the influence of hypoxic conditions, enrichment strategies, and culture medium optimization. Then, we highlight their potential applications in precision oncology, particularly for biomarker discovery and for preclinical drug testing.

Indexed as

NeoplasmsNeoplastic Cells, CirculatingTranslational Research, BiomedicalAnimalsHumansNeoplasm MetastasisCTCCTC linesDTCLiquid biopsyPDX models

Identifiers

PMID41530861
PMCPMC12888287

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.