Evidence map›Paper›PMID 15601859›Full record

ArticleMolecular and cellular biology2005

Lysosomal targeting of E-cadherin: a unique mechanism for the down-regulation of cell-cell adhesion during epithelial to mesenchymal transitions.

Felipe Palacios, Jogender S Tushir, Yasuyuki Fujita, Crislyn D'Souza-Schorey

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 162 papers.

0numbers the graph read from it
0cells of the map it votes in
162citing papers in PubMed
5.3field-weighted citation impact, top 4% 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

162 citing papers in PubMed, 321 citations in OpenAlex.

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  9. Peptide-coated DNA nanostructures as a platform for control of lysosomal function in cells.Chemical engineering journal (Lausanne, Switzerland : 1996) · 2024
    Article
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  12. Vimentin and cytokeratin: Good alone, bad together.Seminars in cancer biology · 2022
    Review
  13. Article
  14. Article
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  17. Heuristic shortest hyperpaths in cell signaling hypergraphs.Algorithms for molecular biology : AMB · 2022
    Article
  18. Review
  19. Article
  20. Article

102 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

4 authors at 2 institutions in 2 countries.

Felipe PalaciosDepartment of Biological Sciences, University of Notre Dame, Box 369, Galvin Life Sciences Bldg., Notre Dame, IN 46556-0369, USA.
Jogender S Tushir
Yasuyuki Fujita
Crislyn D'Souza-Schorey
University of Notre Dame · USMRC Laboratory for Molecular Cell Biology · GB

Funding

Medical Research Council MC_U122669938
6 · The paper itself

Abstract

A hallmark characteristic of epithelial tumor progression as well as some processes of normal development is the loss of the epithelial phenotype and acquisition of a motile or mesenchymal phenotype. Such epithelial to mesenchymal transitions are accompanied by the loss of E-cadherin function by either transcriptional or posttranscriptional mechanisms. Here we demonstrate that, upon v-Src expression, a potent trigger of epithelial to mesenchymal transitions, E-cadherin is internalized and then shuttled to the lysosome instead of being recycled back to the lateral membrane. Thus, while E-cadherin internalization facilitates the dissolution of adherens junctions, its subsequent traffic to the lysosome serves as a means to ensure that cells do not reform their cell-cell contacts and remain motile. We also show that ubiquitin tagging of E-cadherin is essential for its sorting to the lysosome. The lysosomal targeting of E-cadherin is mediated by hepatocyte growth factor-regulated tyrosine kinase substrate (Hrs) and v-Src-induced activation of the Rab5 and Rab7 GTPases. Our studies reveal that the lysosomal targeting of E-cadherin is an important posttranscriptional mechanism to deplete cellular E-cadherin during Src-induced epithelial to mesenchymal transitions.

Indexed as

Down-RegulationAnimalsBiological TransportCadherinsCell AdhesionCell CommunicationCell LineCell MovementCells, CulturedDogsEndosomal Sorting Complexes Required for TransportEndosomesEnzyme ActivationEpithelial CellsImmunoprecipitationLysosomesCadherinsEndosomal Sorting Complexes Required for Transporthepatocyte growth factor-regulated tyrosine kinase substratePhosphoproteinsrab5 GTP-Binding Proteinsrab7 GTP-Binding Proteinsrab GTP-Binding Proteinssrc-Family KinasesUbiquitin

Identifiers

PMID15601859
PMCPMC538771
OpenAlexW1984759958

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.