Evidence map›Paper›PMID 26008969›Full record

ArticleOncotarget2015

Short-term expansion of breast circulating cancer cells predicts response to anti-cancer therapy.

Bee Luan Khoo, Soo Chin Lee, Prashant Kumar, Tuan Zea Tan, Majid Ebrahimi Warkiani, Samuel G W Ow, Sayantani Nandi, Chwee Teck Lim, Jean Paul Thiery

Registry-linked trialAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03256084 (Characterization of Tumoral Circulating Cells According to Stage of Progression of Colorectal Cancers), which is not on this map. Cited by 80 papers.

0numbers the graph read from it
0cells of the map it votes in
80citing 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.

NCT03256084 naunknown statusnot on this mapstarted 2017, after this paper: background citation

Characterization of Tumoral Circulating Cells According to Stage of Progression of Colorectal Cancers

TypeinterventionalSponsorInstitut Paoli-CalmettesRan2017 to 2025Enrolled120ConditionsColorectal CancerArmsBlood and tumor samples
3 · Its place in the literature

Who cites it

80 citing papers in PubMed.

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  19. AnCancer informatics · 2022
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20 more citing papers are in PubMed but not listed here.

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.

Bee Luan KhooMechanobiology Institute, National University of Singapore, Singapore.
Soo Chin LeeDepartment of Hematology-Oncology, National University Cancer Institute, National University Hospital, Singapore.
Prashant KumarInstitute of Molecular and Cell Biology, A*STAR (Agency for Science, Technology and Research), Singapore.
Tuan Zea TanCancer Science Institute of Singapore, National University of Singapore, Singapore.
Majid Ebrahimi WarkianiBioSystems and Micromechanics (BioSyM) IRG, Singapore-MIT Alliance for Research and Technology (SMART) Centre, Singapore.
Samuel G W OwDepartment of Hematology-Oncology, National University Cancer Institute, National University Hospital, Singapore.
Sayantani NandiInstitute of Molecular and Cell Biology, A*STAR (Agency for Science, Technology and Research), Singapore.
Chwee Teck LimInstitute of Molecular and Cell Biology, A*STAR (Agency for Science, Technology and Research), Singapore.
Jean Paul ThieryCancer Science Institute of Singapore, National University of Singapore, Singapore.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Circulating tumor cells (CTCs) are considered as surrogate markers for prognosticating and evaluating patient treatment responses. Here, 226 blood samples from 92 patients with breast cancer, including patients with newly diagnosed or metastatic refractory cancer, and 16 blood samples from healthy subjects were cultured in laser-ablated microwells. Clusters containing an increasing number of cytokeratin-positive (CK+) cells appeared after 2 weeks, while most blood cells disappeared with time. Cultures were heterogeneous and exhibited two distinct sub-populations of cells: 'Small' (≤ 25 μm; high nuclear/cytoplasmic ratio; CD45-) cells, comprising CTCs, and 'Large' (> 25 μm; low nuclear/cytoplasmic ratio; CD68+ or CD56+) cells, corresponding to macrophage and natural killer-like cells. The Small cell fraction also showed copy number increases in six target genes (FGFR1, Myc, CCND1, HER2, TOP2A and ZNF217) associated with breast cancer. These expanded CTCs exhibited different proportions of epithelial-mesenchymal phenotypes and were transferable for further expansion as spheroids in serum-free suspension or 3D cultures. Cluster formation was affected by the presence and duration of systemic therapy, and its persistence may reflect therapeutic resistance. This novel and advanced method estimates CTC clonal heterogeneity and can predict, within a relatively short time frame, patient responses to therapy.

Indexed as

Antineoplastic AgentsBiomarkers, TumorBreast NeoplasmsCyclophosphamideDoxorubicinDrug Resistance, NeoplasmEpithelial-Mesenchymal TransitionFemaleGene DosageHumansIndolesKeratinsMCF-7 CellsNeoplastic Cells, CirculatingPyrrolesSpheroids, CellularAntineoplastic AgentsBiomarkers, TumorCyclophosphamideDoxorubicinIndolesKeratinsPyrrolesSunitinibbreast cancercirculating tumor cellsCTCsenrichment

Identifiers

PMID26008969
PMCPMC4558172

What OpenQuestion holds

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Registered trials

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.