Evidence map›Paper›PMID 25482527›Full record

ArticleCell adhesion & migration2014

EDI3 links choline metabolism to integrin expression, cell adhesion and spreading.

Michaela S Lesjak, Rosemarie Marchan, Joanna D Stewart, Eugen Rempel, Jörg Rahnenführer, Jan G Hengstler

Open access · goldAbstract read
In one paragraph

Article in Cell adhesion & migration, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
1.7field-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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 69 citations in OpenAlex.

  1. Pooled it
  2. Endometrial cancer risk stratification using MRI radiomics: corroborating with choline metabolism.Cancer imaging : the official publication of the International Cancer Imaging Society · 2024
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  15. Integrins and Cell Metabolism: An Intimate Relationship Impacting Cancer.International journal of molecular sciences · 2017
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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

6 authors at 2 institutions in 2 countries.

Michaela S Lesjaka Department of Systems Toxicology ; Leibniz Research Centre for Working Environment and Human Factors ; Dortmund , Germany.
Rosemarie Marchan
Joanna D Stewart
Eugen Rempel
Jörg Rahnenführer
Jan G Hengstler
TU Dortmund University · DEUniversity of Southampton · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Endometrial carcinoma differential 3 (EDI3) was the first member of the glycerophosphodiesterase (GDE) protein family shown to be associated with cancer. Our initial work demonstrated that endometrial and ovarian cancer patients with primary tumors overexpressing EDI3 had a higher risk of developing metastasis and decreased survival. Further analysis indicated that EDI3 cleaves glycerophosphocholine to choline and glycerol-3-phosphate, increases the levels of active PKC, and enhances the migratory activity of tumor cells. Despite these initial findings, EDI3 remained mainly uncharacterized. Therefore, to obtain an overview of processes in which EDI3 may be involved, gene array analysis was performed using MCF-7 breast cancer cells after EDI3 knockdown compared with a non-targeting control siRNA. Several biological motifs were altered, including an enrichment of genes involved in integrin-mediated signaling. More specifically, silencing of EDI3 in MCF-7 and OVCAR-3 cells was associated with reduced expression of the key receptor subunit integrin β1, leading to decreased cell attachment and spreading accompanied by delayed formation of cell protrusions. To confirm these results, we stably overexpressed EDI3 in MCF-7 cells which led to elevated integrin β1 expression associated with enhanced cell attachment and spreading - two processes critical for metastasis. In conclusion, our data provide further insight into the role of EDI3 during cancer progression.

Indexed as

Cell AdhesionCell MovementCholineHumansIntegrinsMCF-7 CellsPhospholipasesCholineGPCPD1 protein, humanIntegrinsPhospholipasesadhesioncholine metabolismDAG, diacylglycerolDHAP, dihydroxyacetone phosphateECM, extracellular matrixEDI3EDI3, Endometrial carcinoma differential 3ER, estrogen receptorFN, fibronectinGDE5GDE, glycerophosphodiesteraseglycerophosphodiesteraseGO, gene ontologyGPC, glycerophosphocholineintegrinsmetastasismigrationPA, phosphatidic acidPC, phosphocholinePKC, protein kinase CPLD, phospholipase DPtdCho, phosphatidylcholinespreading

Identifiers

PMID25482527
PMCPMC4594537
OpenAlexW1969535829

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.