Evidence map›Paper›PMID 31446534›Full record

ArticleInvestigational new drugs2020

Effects of salinomycin and niclosamide on small cell lung cancer and small cell lung cancer circulating tumor cell lines.

Maximilian Hochmair, Barbara Rath, Lukas Klameth, Ernst Ulsperger, Christoph Weinlinger, Andreas Fazekas, Adelina Plangger, Robert Zeillinger, Gerhard Hamilton

Open access · hybridAbstract read
In one paragraph

Article in Investigational new drugs, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 23% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

  1. Pooled it
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  3. Review
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  8. Article
  9. [A Rare Case of Extremely High Counts of EpCAMSichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition · 2022
    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 2 institutions in 1 country.

Maximilian HochmairRespiratory Oncology Unit, Otto Wagner Hospital, Baumgartner Höhe, Vienna, Austria.
Barbara RathDepartment of Surgery, Medical University of Vienna, Spitalgasse, Vienna, Austria.
Lukas KlamethDepartment of Pathophysiology and Allergy Research, Medical University of Vienna, Vienna, Austria.
Ernst UlspergerHospital Horn, Spitalgasse, Horn, Austria.
Christoph WeinlingerRespiratory Oncology Unit, Otto Wagner Hospital, Baumgartner Höhe, Vienna, Austria.
Andreas FazekasRespiratory Oncology Unit, Otto Wagner Hospital, Baumgartner Höhe, Vienna, Austria.
Adelina PlanggerDepartment of Surgery, Medical University of Vienna, Spitalgasse, Vienna, Austria.
Robert ZeillingerDepartment of Gynecology and Obstetrics, Molecular Oncology Group, Medical University of Vienna, Vienna, Austria.
Gerhard HamiltonDepartment of Surgery, Medical University of Vienna, Spitalgasse, Vienna, Austria. gerhard.hamilton@meduniwien.ac.at.
Medical University of Vienna · ATOtto Wagner Hospital · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumor dissemination and recurrence is attributed to highly resistant cancer stem cells (CSCs) which may constitute a fraction of circulating tumor cells (CTCs). Small cell lung cancer (SCLC) constitutes a suitable model to investigate the relation of CTCs and CSCs due to rapid tumor spread and a high number of CTCs. Expansion of five SCLC CTC lines (BHGc7, 10, 16, 26 and UHGc5) in vitro at our institution allowed for the analysis of CSC markers and cytotoxicity of the CSC-selective drugs salinomycin and niclosamide against CTC single cell suspensions or CTC spheroids/ tumorospheres (TOS). Salinomycin exerted dose-dependent cytotoxicity against the SCLC lines but, with exception of BHGc7 TOS, there was no markedly enhanced activity against TOS. Similarly, niclosamide exhibits high activity against BHGc7 TOS and UHGc5 TOS but not against the other CTC spheroids. High expression of the CSC marker CD133 was restricted to three SCLC tumor lines and the BHGc10 CTC line. All SCLC CTCs are CD24-positive but lack expression of CD44 and ABCG2 in contrast to the SCLC tumor lines which show a phenotype more similar to that of CSCs. The stem cell marker SOX2 was found in all CTC lines and SCLC GLC14/16, whereas elevated expression of Oct-3/4 and Nanog was restricted to BHGc26 and UHGc5. In conclusion, the SCLC CTCs established from patients with relapsed disease lack a typical CSC phenotype in respect to chemosensitivity to CSC-selective drugs, surface markers, expression of pluripotent stem cell and transcription factors.

Indexed as

Antigens, CDAntineoplastic AgentsCell LineCell ProliferationCell SurvivalHumansLung NeoplasmsNanog Homeobox ProteinNeoplastic Cells, CirculatingNeoplastic Stem CellsNiclosamideOctamer Transcription Factor-3Polyether PolyketidesPyransSmall Cell Lung CarcinomaSOXB1 Transcription FactorsAntigens, CDAntineoplastic AgentsNanog Homeobox ProteinNANOG protein, humanNiclosamideOctamer Transcription Factor-3Polyether PolyketidesPOU5F1 protein, humanPyranssalinomycinSOX2 protein, humanSOXB1 Transcription FactorsCancer stem cellsCD133Circulating tumor cellsCytotoxicityNiclosamideSalinomycinSmall cell lung cancer

Identifiers

PMID31446534
PMCPMC7340652
OpenAlexW2969299486

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.