Evidence map›Paper›PMID 42151560›Full record

ArticleBritish journal of cancer2026

Circulating tumour cell-derived xenograft as a preclinical platform for metastatic breast cancer.

Zuzana Kahounová, Markéta Hrušková, Stanislav Drápela, Ondřej Naar, Ráchel Víchová, Jiří Navrátil, Pavel Fabian, Filip Zavadil Kokáš, Aleš Hampl, Jan Bouchal and 1 more

Abstract read
In one paragraph

Article in British journal of cancer, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
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

11 authors.

Zuzana KahounováDepartment of Cytokinetics, Institute of Biophysics of the Czech Academy of Sciences, Brno, Czech Republic.
Markéta HruškováDepartment of Cytokinetics, Institute of Biophysics of the Czech Academy of Sciences, Brno, Czech Republic.
Stanislav DrápelaDepartment of Cytokinetics, Institute of Biophysics of the Czech Academy of Sciences, Brno, Czech Republic.
Ondřej NaarDepartment of Cytokinetics, Institute of Biophysics of the Czech Academy of Sciences, Brno, Czech Republic.
Ráchel VíchováDepartment of Cytokinetics, Institute of Biophysics of the Czech Academy of Sciences, Brno, Czech Republic.
Jiří NavrátilDepartment of Comprehensive Cancer Care, Masaryk Memorial Cancer Institute, Brno, Czech Republic.
Pavel FabianDepartment of Oncological Pathology, Masaryk Memorial Cancer Institute, Brno, Czech Republic.
Filip Zavadil KokášDepartment of Bioinformatics, RECAMO, Masaryk Memorial Cancer Institute, Brno, Czech Republic.
Aleš HamplInternational Clinical Research Center, St. Anne's University Hospital, Brno, Czech Republic.
Jan BouchalDepartment of Clinical and Molecular Pathology, Institute of Molecular and Translational Medicine, Faculty of Medicine and Dentistry, Palacky University and University Hospital, Olomouc, Czech Republic.
Karel SoučekDepartment of Cytokinetics, Institute of Biophysics of the Czech Academy of Sciences, Brno, Czech Republic. ksoucek@ibp.cz.ORCID http://orcid.org/0000-0001-7283-8150

Funding

Agentura Pro Zdravotnický Výzkum České Republiky (Czech Health Research Council) NU21-08-00023Ministerstvo Školství, Mládeže a Tělovýchovy (Ministry of Education, Youth and Sports) Programme EXCELES, ID Project No. LX22NPO5102Ministerstvo Zdravotnictví Ceské Republiky (Ministry of Health of the Czech Republic) MMCI 00209805
6 · The paper itself

Abstract

backgroundCirculating tumour cells (CTCs) are mediators of cancer dissemination and the formation of metastasis, which is the leading cause of cancer-related deaths. Experimental models derived from CTCs contribute to understanding the biology of CTCs, their role in dissemination, and the discovery of potential drugs targeting CTCs.

methodsA xenograft was derived from CTCs isolated from a patient diagnosed with metastatic invasive ductal carcinoma of the breast. The characterisation of the CTCs-derived xenograft (CDX) was conducted through in vivo experimental metastatic assays, RNA-Seq, spectral flow cytometry, and drug sensitivity tests.

resultsThe CTCs-enriched fraction formed a CDX within 6 months, and its metastatic potential was confirmed. CDX cells were propagated in vitro, where the enrichment of CD44

conclusionsWe present and characterise a novel model derived from CTCs for understanding the plasticity and behaviour of CTCs and advanced breast cancer. CDX_IBP_01 was established from the CTC-enriched fraction obtained from the patient with progressing breast cancer. Once stably re-transplanted and growing in vivo, the transcriptomes of CDX and archived primary BCa1 samples were compared. 2D and 3D in vitro cell cultures were established from sorted human cancer cells from an in vivo xenograft. Phenotypes of established models and their stability were characterised using spectral flow cytometry. The metastatic potential of CDX was evaluated in an in vivo assay. Finally, the applicability of the established model for in vivo and in vitro drug screening was evaluated. Created in https://BioRender.com .

Indexed as

Breast NeoplasmsCarcinoma, Ductal, BreastNeoplastic Cells, CirculatingAnimalsAntineoplastic AgentsFemaleHeterograftsHumansMiceNeoplasm MetastasisNeoplastic Stem CellsPiperidinesQuinazolinesXenograft Model Antitumor AssaysAntineoplastic AgentsPiperidinesQuinazolinesvandetanib

Identifiers

PMID42151560
PMCPMC13427727

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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.