Evidence map›Paper›PMID 29462126›Full record

ArticleBritish journal of cancer2018

Plasticity and intratumoural heterogeneity of cell surface antigen expression in breast cancer.

Ján Remšík, Radek Fedr, Jiří Navrátil, Lucia Binó, Eva Slabáková, Pavel Fabian, Marek Svoboda, Karel Souček

Open access · hybridAbstract read
In one paragraph

Article in British journal of cancer, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.2field-weighted citation impact, top 17% 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

24 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Role of immunotherapy in Ewing sarcoma.Journal for immunotherapy of cancer · 2020
    Review
  19. Article
  20. 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

8 authors at 4 institutions in 1 country.

Ján RemšíkInstitute of Biophysics of the Czech Academy of Sciences, Královopolská 135, Brno 612 65, Czech Republic.
Radek FedrInstitute of Biophysics of the Czech Academy of Sciences, Královopolská 135, Brno 612 65, Czech Republic.
Jiří NavrátilDepartment of Comprehensive Cancer Care, Masaryk Memorial Cancer Institute, Žlutý kopec 7, Brno 656 53, Czech Republic.
Lucia BinóInstitute of Biophysics of the Czech Academy of Sciences, Královopolská 135, Brno 612 65, Czech Republic.
Eva SlabákováInstitute of Biophysics of the Czech Academy of Sciences, Královopolská 135, Brno 612 65, Czech Republic.
Pavel FabianDepartment of Oncological Pathology, Masaryk Memorial Cancer Institute, Žlutý kopec 7, Brno 656 53, Czech Republic.
Marek SvobodaDepartment of Comprehensive Cancer Care, Masaryk Memorial Cancer Institute, Žlutý kopec 7, Brno 656 53, Czech Republic.
Karel SoučekInstitute of Biophysics of the Czech Academy of Sciences, Královopolská 135, Brno 612 65, Czech Republic.
Czech Academy of Sciences, Institute of Biophysics · CZMasaryk Memorial Cancer Institute · CZSt. Anne's University Hospital Brno · CZUniversity Hospital Brno · CZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background:The intratumoural heterogeneity, often driven by epithelial-to-mesenchymal transition (EMT), significantly contributes to chemoresistance and disease progression in adenocarcinomas. Methods:We introduced a high-throughput screening platform to identify surface antigens that associate with epithelial–mesenchymal plasticity in well-defined pairs of epithelial cell lines and their mesenchymal counterparts. Using multicolour flow cytometry, we then analysed the expression of 10 most robustly changed antigens and identified a 10-molecule surface signature, in pan-cytokeratin-positive/EpCAM-positive and -negative fractions of dissociated breast tumours. Results:We found that surface CD9, CD29, CD49c, and integrin ß5 are lost in breast cancer cells that underwent EMT in vivo. The tetraspanin family member CD9 was concordantly downregulated both in vitro and in vivo and associated with epithelial phenotype and favourable prognosis. Conclusions:We propose that overall landscape of 10-molecule surface signature expression reflects the epithelial–mesenchymal plasticity in breast cancer.

Indexed as

Antigens, NeoplasmAntigens, SurfaceBiomarkers, TumorBreast NeoplasmsCell Line, TumorCell PlasticityCellular ReprogrammingEpithelial-Mesenchymal TransitionFemaleFlow CytometryHigh-Throughput Screening AssaysHumansNeoplasm MetastasisTetraspanin 29Transcription, GeneticAntigens, NeoplasmAntigens, SurfaceBiomarkers, TumorCD9 protein, humanTetraspanin 29

Identifiers

PMID29462126
PMCPMC5886127
OpenAlexW2792921066

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.