Evidence map›Paper›PMID 24880617›Full record

ArticleNature medicine2014

Tumorigenicity and genetic profiling of circulating tumor cells in small-cell lung cancer.

Cassandra L Hodgkinson, Christopher J Morrow, Yaoyong Li, Robert L Metcalf, Dominic G Rothwell, Francesca Trapani, Radoslaw Polanski, Deborah J Burt, Kathryn L Simpson, Karen Morris and 16 more

Registry-linked trialAbstract read
PubMed Publisher
In one paragraph

Article in Nature medicine, 2014. 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 409 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
409citing papers in PubMed, 1 pooled it
39.4field-weighted citation impact, top 1% 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.

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

409 citing papers in PubMed, 1 synthesis or guideline pooled it, 688 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
  4. Review
  5. YAP1 Defines an Emergent, Plastic Population of Relapsed SCLC.Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer · 2026
    Article
  6. Article
  7. Review
  8. Circulating Tumor Cells: Emerging Frontiers in Cancer Technology.Expert reviews in molecular medicine · 2026
    Review
  9. Review
  10. Observational
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. Review
  20. Article

349 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

26 authors at 3 institutions in 1 country.

Cassandra L Hodgkinson1] Clinical and Experimental Pharmacology Group, Cancer Research UK Manchester Institute, University of Manchester, Manchester, UK. [2].
Christopher J Morrow1] Clinical and Experimental Pharmacology Group, Cancer Research UK Manchester Institute, University of Manchester, Manchester, UK. [2].
Yaoyong LiComputational Biology Support Group, Cancer Research UK Manchester Institute, University of Manchester, Manchester, UK.
Robert L MetcalfClinical and Experimental Pharmacology Group, Cancer Research UK Manchester Institute, University of Manchester, Manchester, UK.
Dominic G RothwellClinical and Experimental Pharmacology Group, Cancer Research UK Manchester Institute, University of Manchester, Manchester, UK.
Francesca TrapaniClinical and Experimental Pharmacology Group, Cancer Research UK Manchester Institute, University of Manchester, Manchester, UK.
Radoslaw PolanskiClinical and Experimental Pharmacology Group, Cancer Research UK Manchester Institute, University of Manchester, Manchester, UK.
Deborah J BurtClinical and Experimental Pharmacology Group, Cancer Research UK Manchester Institute, University of Manchester, Manchester, UK.
Kathryn L SimpsonClinical and Experimental Pharmacology Group, Cancer Research UK Manchester Institute, University of Manchester, Manchester, UK.
Karen MorrisClinical and Experimental Pharmacology Group, Cancer Research UK Manchester Institute, University of Manchester, Manchester, UK.
Stuart D PepperMolecular Biology Core Facility, Cancer Research UK Manchester Institute, University of Manchester, Manchester, UK.
Daisuke NonakaThe Christie NHS Foundation Trust, Manchester, UK.
Alastair Greystoke1] Clinical and Experimental Pharmacology Group, Cancer Research UK Manchester Institute, University of Manchester, Manchester, UK. [2] The Christie NHS Foundation Trust, Manchester, UK. [3] Institute of Cancer Sciences, University of Manchester, Manchester, UK.
Paul KellyClinical and Experimental Pharmacology Group, Cancer Research UK Manchester Institute, University of Manchester, Manchester, UK.
Becky BolaClinical and Experimental Pharmacology Group, Cancer Research UK Manchester Institute, University of Manchester, Manchester, UK.
Matthew G KrebsClinical and Experimental Pharmacology Group, Cancer Research UK Manchester Institute, University of Manchester, Manchester, UK.
Jenny AntonelloClinical and Experimental Pharmacology Group, Cancer Research UK Manchester Institute, University of Manchester, Manchester, UK.
Mahmood AyubClinical and Experimental Pharmacology Group, Cancer Research UK Manchester Institute, University of Manchester, Manchester, UK.
Suzanne FaulknerClinical and Experimental Pharmacology Group, Cancer Research UK Manchester Institute, University of Manchester, Manchester, UK.
Lynsey PriestClinical and Experimental Pharmacology Group, Cancer Research UK Manchester Institute, University of Manchester, Manchester, UK.
Louise CarterClinical and Experimental Pharmacology Group, Cancer Research UK Manchester Institute, University of Manchester, Manchester, UK.
Catriona TateClinical and Experimental Pharmacology Group, Cancer Research UK Manchester Institute, University of Manchester, Manchester, UK.
Crispin J Miller1] Computational Biology Support Group, Cancer Research UK Manchester Institute, University of Manchester, Manchester, UK. [2] RNA Biology Group, Cancer Research UK Manchester Institute, University of Manchester, Manchester, UK.
Fiona Blackhall1] The Christie NHS Foundation Trust, Manchester, UK. [2] Institute of Cancer Sciences, University of Manchester, Manchester, UK. [3].
Ged Brady1] Clinical and Experimental Pharmacology Group, Cancer Research UK Manchester Institute, University of Manchester, Manchester, UK. [2].
Caroline Dive1] Clinical and Experimental Pharmacology Group, Cancer Research UK Manchester Institute, University of Manchester, Manchester, UK. [2].
University of Manchester · GBCancer Research UK Manchester Institute · GBThe Christie NHS Foundation Trust · GB

Funding

Cancer Research UK 15675Cancer Research UK 19278Cancer Research UK C1467/A15578Cancer Research UK C5759/A12328
6 · The paper itself

Abstract

Small-cell lung cancer (SCLC), an aggressive neuroendocrine tumor with early dissemination and dismal prognosis, accounts for 15-20% of lung cancer cases and ∼200,000 deaths each year. Most cases are inoperable, and biopsies to investigate SCLC biology are rarely obtainable. Circulating tumor cells (CTCs), which are prevalent in SCLC, present a readily accessible 'liquid biopsy'. Here we show that CTCs from patients with either chemosensitive or chemorefractory SCLC are tumorigenic in immune-compromised mice, and the resultant CTC-derived explants (CDXs) mirror the donor patient's response to platinum and etoposide chemotherapy. Genomic analysis of isolated CTCs revealed considerable similarity to the corresponding CDX. Most marked differences were observed between CDXs from patients with different clinical outcomes. These data demonstrate that CTC molecular analysis via serial blood sampling could facilitate delivery of personalized medicine for SCLC. CDXs are readily passaged, and these unique mouse models provide tractable systems for therapy testing and understanding drug resistance mechanisms.

Indexed as

AnimalsBiomarkers, TumorCell Transformation, NeoplasticDisease Models, AnimalDrug Resistance, NeoplasmFemaleHumansLung NeoplasmsMiceMice, Inbred NODMolecular Sequence DataNeoplasm MetastasisNeoplasm TransplantationNeoplastic Cells, CirculatingSmall Cell Lung CarcinomaTransplantation, HeterologousBiomarkers, Tumor

Identifiers

PMID24880617
OpenAlexW2088942535

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.