Evidence map›Paper›PMID 19287376›Full record

ArticleNature cell biology2009

Characterization of the interface between normal and transformed epithelial cells.

Catherine Hogan, Sophie Dupré-Crochet, Mark Norman, Mihoko Kajita, Carola Zimmermann, Andrew E Pelling, Eugenia Piddini, Luis Alberto Baena-López, Jean-Paul Vincent, Yoshifumi Itoh and 3 more

Abstract readLetter
PubMed Publisher
In one paragraph

Article in Nature cell biology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 182 papers.

0numbers the graph read from it
0cells of the map it votes in
182citing papers in PubMed
7.1field-weighted citation impact, top 2% 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

182 citing papers in PubMed, 361 citations in OpenAlex.

  1. Article
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  14. Article
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  16. Clonal effects of thebioRxiv : the preprint server for biology · 2025
    Article
  17. Article
  18. Cell extrusion drives neural crest cell delamination.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  19. Drosophila as a Model for Metastasis.Advances in experimental medicine and biology · 2025
    Review
  20. Review

122 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

13 authors at 6 institutions in 3 countries.

Catherine Hogan
Sophie Dupré-Crochet
Mark Norman
Mihoko Kajita
Carola Zimmermann
Andrew E Pelling
Eugenia Piddini
Luis Alberto Baena-López
Jean-Paul Vincent
Yoshifumi Itoh
Hiroshi Hosoya
Franck Pichaud
Yasuyuki Fujita
MRC Laboratory for Molecular Cell Biology · GBNational Institute for Health Research · GBUniversity College London · GBHiroshima University · JPImperial College London · GBLondon Centre for Nanotechnology · GB

Funding

Medical Research Council G0802007Medical Research Council MC_U117584268Medical Research Council MC_U122669938Medical Research Council MC_U122673973
6 · The paper itself

Abstract

In most cancers, transformation begins in a single cell in an epithelial cell sheet. However, it is not known what happens at the interface between non-transformed (normal) and transformed cells once the initial transformation has occurred. Using Madin-Darby canine kidney (MDCK) epithelial cells that express constitutively active, oncogenic Ras (Ras(V12)) in a tetracycline-inducible system, we investigated the cellular processes arising at the interface between normal and transformed cells. We show that two independent phenomena occur in a non-cell-autonomous manner: when surrounded by normal cells, Ras(V12) cells are either apically extruded from the monolayer, or form dynamic basal protrusions and invade the basal matrix. Neither apical extrusion nor basal protrusion formation is observed when Ras(V12) cells are surrounded by other Ras(V12) cells. We show that Cdc42 and ROCK (also known as Rho kinase) have vital roles in these processes. We also demonstrate that E-cadherin knockdown in normal cells surrounding Ras(V12) cells reduces the frequency of apical extrusion, while promoting basal protrusion formation and invasion. These results indicate that Ras(V12)-transformed cells are able to recognize differences between normal and transformed cells, and consequently leave epithelial sheets either apically or basally, in a cell-context-dependent manner.

Indexed as

AnimalsCadherinsCell LineageCell PolarityCell Transformation, NeoplasticDogsEpithelial CellsEpitheliumGreen Fluorescent ProteinsPseudopodiaras ProteinsRecombinant Fusion ProteinsCadherinsGreen Fluorescent Proteinsras ProteinsRecombinant Fusion Proteins

Identifiers

PMID19287376
OpenAlexW2039898135

What OpenQuestion holds

Textmetadata
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.