Evidence map›Paper›PMID 34821540›Full record

ReviewTissue barriers2022

Dual role of E-cadherin in cancer cells.

Svetlana N Rubtsova, Irina Y Zhitnyak, Natalya A Gloushankova

Open access · greenAbstract readReview
In one paragraph

Review in Tissue barriers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

63 citing papers in PubMed, 81 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review

3 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

3 authors.

Svetlana N RubtsovaN.N. Blokhin National Medical Research Center of Oncology, Institute of Carcinogenesis, Moscow, Russia.ORCID 0000-0003-4620-7851
Irina Y ZhitnyakN.N. Blokhin National Medical Research Center of Oncology, Institute of Carcinogenesis, Moscow, Russia.ORCID 0000-0002-6717-3745
Natalya A GloushankovaN.N. Blokhin National Medical Research Center of Oncology, Institute of Carcinogenesis, Moscow, Russia.ORCID 0000-0002-2044-2063

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

E-cadherin is the main component of epithelial adherens junctions (AJs), which play a crucial role in the maintenance of stable cell-cell adhesion and overall tissue integrity. Down-regulation of E-cadherin expression has been found in many carcinomas, and loss of E-cadherin is generally associated with poor prognosis in patients. During the last decade, however, numerous studies have shown that E-cadherin is essential for several aspects of cancer cell biology that contribute to cancer progression, most importantly, active cell migration. In this review, we summarize the available data about the input of E-cadherin in cancer progression, focusing on the latest advances in the research of the various roles E-cadherin-based AJs play in cancer cell dissemination. The review also touches upon the "cadherin switching" in cancer cells where N- or P-cadherin replace or are co-expressed with E-cadherin and its influence on the migratory properties of cancer cells.

Indexed as

Epithelial-Mesenchymal TransitionNeoplasmsAdherens JunctionsCadherinsCell AdhesionCell MovementHumansCadherinsactin cytoskeletonAdherens junctionsadhesioncancerE-cadherinEMTinvasion-metastasis cascade

Identifiers

PMID34821540
PMCPMC9621038
OpenAlexW3215169467

What Socratic 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 Socratic graph.