Evidence map›Paper›PMID 37566019›Full record

ArticleCells2023

Functional Analysis of Viable Circulating Tumor Cells from Triple-Negative Breast Cancer Patients Using TetherChip Technology.

Vasileios Vardas, Julia A Ju, Athina Christopoulou, Anastasia Xagara, Vassilis Georgoulias, Athanasios Kotsakis, Catherine Alix-Panabières, Stuart S Martin, Galatea Kallergi

Open access · goldAbstract read
In one paragraph

Article in Cells, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

7 citing papers in PubMed, 9 citations in OpenAlex.

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  6. ES-SCLC Patients with PD-L1Biomedicines · 2024
    Article
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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

9 authors at 6 institutions in 3 countries.

Vasileios VardasLaboratory of Biochemistry/Metastatic Signaling, Section of Genetics, Cell Biology and Development, Department of Biology, University of Patras, GR-26504 Patras, Greece.ORCID 0000-0002-1717-9196
Julia A JuDepartment of Pharmacology, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
Athina ChristopoulouOncology Unit, ST Andrews General Hospital of Patras, GR-26332 Patras, Greece.
Anastasia XagaraLaboratory of Oncology, Faculty of Medicine, School of Health Sciences, University of Thessaly, GR-41110 Larissa, Greece.ORCID 0000-0001-8104-1514
Vassilis GeorgouliasHellenic Oncology Research Group (HORG), GR-11526 Athens, Greece.ORCID 0000-0003-2218-2522
Athanasios KotsakisLaboratory of Oncology, Faculty of Medicine, School of Health Sciences, University of Thessaly, GR-41110 Larissa, Greece.ORCID 0000-0002-5530-6774
Catherine Alix-PanabièresLaboratory of Rare Human Circulating Cells (LCCRH), University Medical Center of Montpellier, 34295 Montpellier, France.ORCID 0000-0002-6401-2903
Stuart S MartinDepartment of Pharmacology, University of Maryland School of Medicine, Baltimore, MD 21201, USA.ORCID 0000-0002-4378-4381
Galatea KallergiLaboratory of Biochemistry/Metastatic Signaling, Section of Genetics, Cell Biology and Development, Department of Biology, University of Patras, GR-26504 Patras, Greece.
University of Maryland, Baltimore · USUniversity of Patras · GRUniversity of Thessaly · GRCentre National de la Recherche Scientifique · FRGeneral University Hospital of Patras · GRHellenic Oncology Research Group · GR

Funding

Targeting microtubule stabilization to reduce breast tumor metastasisR01CA154624 · NCI · UNIVERSITY OF MARYLAND BALTIMORE · PI MARTIN, STUART S · 2012 to 2023
$3.4M
NCI NIH HHS R01 CA154624
6 · The paper itself

Abstract

Metastasis, rather than the growth of the primary tumor, accounts for approximately 90% of breast cancer patient deaths. Microtentacles (McTNs) formation represents an important mechanism of metastasis. Triple-negative breast cancer (TNBC) is the most aggressive subtype with limited targeted therapies. The present study aimed to isolate viable circulating tumor cells (CTCs) and functionally analyze them in response to drug treatment. CTCs from 20 TNBC patients were isolated and maintained in culture for 5 days. Biomarker expression was identified by immunofluorescence staining and VyCap analysis. Vinorelbine-induced apoptosis was evaluated based on the detection of M30-positive cells. Our findings revealed that the CTC absolute number significantly increased using TetherChips analysis compared to the number of CTCs in patients' cytospins (

Indexed as

Neoplastic Cells, CirculatingTriple Negative Breast NeoplasmsBiomarkers, TumorCell Line, TumorHumansPilot ProjectsVinorelbineBiomarkers, TumorVinorelbinecirculating tumor cellsEMTimmune checkpointsmetastasistriple-negative breast cancervinorelbine

Identifiers

PMID37566019
PMCPMC10416943
OpenAlexW4385359046

What OpenQuestion holds

Textmetadata
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.