Evidence map›Paper›PMID 19491271›Full record

ArticleCancer research2009

Loss of retinal cadherin facilitates mammary tumor progression and metastasis.

Georgia Agiostratidou, Maomi Li, Kimita Suyama, Ines Badano, Rinat Keren, Su Chung, Amy Anzovino, James Hulit, Binzhi Qian, Boumediene Bouzahzah and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer research, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

31 citing papers in PubMed, 53 citations in OpenAlex.

  1. Article
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  5. Expression and associated epigenetic mechanisms of the CaJournal of cell communication and signaling · 2022
    Article
  6. Review
  7. Article
  8. Article
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  11. Expression and Prognostic Significance of Cadherin 4 (CDH4) in Renal Cell Carcinoma.Medical science monitor : international medical journal of experimental and clinical research · 2020
    Article
  12. Article
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  15. Article
  16. Review
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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

15 authors at 3 institutions in 1 country.

Georgia AgiostratidouDepartment of Pathology, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Maomi Li
Kimita Suyama
Ines Badano
Rinat Keren
Su Chung
Amy Anzovino
James Hulit
Binzhi Qian
Boumediene Bouzahzah
Eliseo Eugenin
Olivier Loudig
Greg R Phillips
Joseph Locker
Rachel B Hazan
Albert Einstein College of Medicine · USIcahn School of Medicine at Mount Sinai · USMontefiore Medical Center · US

Funding

R-Cadherin in Breast Cancer SuppressionR01CA136854 · NCI · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI HAZAN, RACHEL B · 2009 to 2013
$1.7M
Mechanisms of N-Cadherin Mediated Breast CA MetastasisR01CA090872 · NCI · YESHIVA UNIVERSITY · PI HAZAN, RACHEL B · 2002 to 2005
$1.2M
The role of gap junction channels in NeuroAIDSK01MH076679 · NIMH · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI EUGENIN, ELISEO A · 2006 to 2010
$646k
NCI NIH HHS 1R01 CA90872NCI NIH HHS R01 CA090872NCI NIH HHS R01 CA136854NIMH NIH HHS K01 MH076679
6 · The paper itself

Abstract

The mammary epithelium is thought to be stabilized by cell-cell adhesion mediated mainly by E-cadherin (E-cad). Here, we show that another cadherin, retinal cadherin (R-cad), is critical for maintenance of the epithelial phenotype. R-cad is expressed in nontransformed mammary epithelium but absent from tumorigenic cell lines. In vivo, R-cad was prominently expressed in the epithelium of both ducts and lobules. In human breast cancer, R-cad was down-regulated with tumor progression, with high expression in ductal carcinoma in situ and reduced expression in invasive duct carcinomas. By comparison, E-cad expression persisted in invasive breast tumors and cell lines where R-cad was lost. Consistent with these findings, R-cad knockdown in normal mammary epithelium stimulated invasiveness and disrupted formation of acini despite continued E-cad expression. Conversely, R-cad overexpression in aggressive cell lines induced glandular morphogenesis and inhibited invasiveness, tumor formation, and lung colonization. R-cad also suppressed the matrix metalloproteinase 1 (MMP1), MMP2, and cyclooxygenase 2 gene expression associated with pulmonary metastasis. The data suggest that R-cad is an adhesion molecule of the mammary epithelium, which acts as a critical regulator of the normal phenotype. As a result, R-cad loss contributes to epithelial suppression and metastatic progression.

Indexed as

Neoplasm MetastasisAnimalsBase SequenceCadherinsCell LineDNA PrimersFemaleHumansImmunohistochemistryMammary Neoplasms, ExperimentalMiceMice, Inbred BALB CNeoplasm InvasivenessPolymerase Chain ReactionRetinaRNA, Small InterferingCadherinsDNA PrimersR-cadherinRNA, Small Interfering

Identifiers

PMID19491271
PMCPMC4382672
OpenAlexW2149953341

What OpenQuestion holds

Textmetadata
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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.