Evidence map›Paper›PMID 24586258›Full record

ArticlePloS one2014

Staurosporine and extracellular matrix proteins mediate the conversion of small cell lung carcinoma cells into a neuron-like phenotype.

Tamara Murmann, Carmen Carrillo-García, Nadine Veit, Cornelius Courts, Alexander Glassmann, Viktor Janzen, Burkhard Madea, Markus Reinartz, Anne Harzen, Michael Nowak and 3 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. 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
0.3field-weighted citation impact, top 39% 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, 8 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Oncogenic relevant defensins: expression pattern and proliferation characteristics of human tumor cell lines.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Article
  7. Staurosporine analogs promote distinct patterns of process outgrowth and polyploidy in small cell lung carcinoma cells.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2015
    Article
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

13 authors at 3 institutions in 1 country.

Tamara MurmannNeuro- and Tumor Cell Biology Group, Department of Nuclear Medicine, University Hospital of Bonn, Bonn, Germany.
Carmen Carrillo-GarcíaDepartment of Hematology and Oncology, University Hospital of Bonn, Bonn, Germany.
Nadine VeitNeuro- and Tumor Cell Biology Group, Department of Nuclear Medicine, University Hospital of Bonn, Bonn, Germany.
Cornelius CourtsInstitute of Legal Medicine, University of Bonn, Bonn, Germany.
Alexander GlassmannInstitute of Anatomy and Cell Biology, University of Bonn, Bonn, Germany.
Viktor JanzenDepartment of Hematology and Oncology, University Hospital of Bonn, Bonn, Germany.
Burkhard MadeaInstitute of Legal Medicine, University of Bonn, Bonn, Germany.
Markus ReinartzOral Cell Biology Group, Department of Periodontology, Operative and Preventive Dentistry, Bonn, Germany.
Anne HarzenProteomics Group, Max-Planck-Institute for Plant Breeding Research, Cologne, Germany.
Michael NowakDepartment of Prostate Cancer Research, Institute of Pathology, University Hospital of Bonn, Bonn, Germany.
Sven PernerDepartment of Prostate Cancer Research, Institute of Pathology, University Hospital of Bonn, Bonn, Germany.
Jochen WinterOral Cell Biology Group, Department of Periodontology, Operative and Preventive Dentistry, Bonn, Germany.
Rainer ProbstmeierNeuro- and Tumor Cell Biology Group, Department of Nuclear Medicine, University Hospital of Bonn, Bonn, Germany.
University Hospital Bonn · DEUniversity of Bonn · DEMax Planck Institute for Plant Breeding Research · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Small cell lung carcinomas (SCLCs) represent highly aggressive tumors with an overall five-year survival rate in the range of 5 to 10%. Here, we show that four out of five SCLC cell lines reversibly develop a neuron-like phenotype on extracellular matrix constituents such as fibronectin, laminin or thrombospondin upon staurosporine treatment in an RGD/integrin-mediated manner. Neurite-like processes extend rapidly with an average speed of 10 µm per hour. Depending on the cell line, staurosporine treatment affects either cell cycle arrest in G2/M phase or induction of polyploidy. Neuron-like conversion, although not accompanied by alterations in the expression pattern of a panel of neuroendocrine genes, leads to changes in protein expression as determined by two-dimensional gel electrophoresis. It is likely that SCLC cells already harbour the complete molecular repertoire to convert into a neuron-like phenotype. More extensive studies are needed to evaluate whether the conversion potential of SCLC cells is suitable for therapeutic interventions.

Indexed as

Blotting, WesternCell AdhesionCell DifferentiationCell Line, TumorCell ProliferationElectrophoresis, Gel, Two-DimensionalExtracellular Matrix ProteinsFlow CytometryHumansReverse Transcriptase Polymerase Chain ReactionSmall Cell Lung CarcinomaStaurosporineExtracellular Matrix ProteinsStaurosporine

Identifiers

PMID24586258
PMCPMC3938400
OpenAlexW2050839463

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.