Evidence map›Paper›PMID 29059157›Full record

ArticleOncogene2018

EphrinB1 promotes cancer cell migration and invasion through the interaction with RhoGDI1.

H J Cho, Y-S Hwang, J Yoon, M Lee, H G Lee, I O Daar

Open access · hybridAbstract read
In one paragraph

Article in Oncogene, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 23% 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

29 citing papers in PubMed, 1 synthesis or guideline pooled it, 52 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Neuronal guidance behaviours: the primary cilium perspective.Frontiers in cell and developmental biology · 2025
    Review
  6. Article
  7. [Overexpression of CDHR2 inhibits proliferation of breast cancer cells by inhibiting the PI3K/Akt pathway].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2024
    Article
  8. Article
  9. RhoGDI1 regulates cell-cell junctions in polarized epithelial cells.Frontiers in cell and developmental biology · 2024
    Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
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  18. 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

6 authors at 3 institutions in 2 countries.

H J ChoImmunotherapy Convergence Research Center, Korea Research Institute of Bioscience and Biotechnology, Yuseong-gu, Daejeon, Korea.
Y-S HwangCancer & Developmental Biology Laboratory, National Cancer Institute, National Institutes of Health, Frederick, MD, USA.
J YoonCancer & Developmental Biology Laboratory, National Cancer Institute, National Institutes of Health, Frederick, MD, USA.
M LeeCancer & Developmental Biology Laboratory, National Cancer Institute, National Institutes of Health, Frederick, MD, USA.
H G LeeImmunotherapy Convergence Research Center, Korea Research Institute of Bioscience and Biotechnology, Yuseong-gu, Daejeon, Korea.
I O DaarCancer & Developmental Biology Laboratory, National Cancer Institute, National Institutes of Health, Frederick, MD, USA.
National Cancer Institute · USNational Institutes of Health · USKorea Research Institute of Bioscience and Biotechnology · KR

Funding

Mechanisms of Cross-talk Between EphrinB and Alternate Signaling PathwaysZIABC010006 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI DAAR, IRA · 2009 to 2025
$11.5M
Signaling Mechanisms of EphrinB1 in Cell Adhesion, Migration and InvasionZIABC010958 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI DAAR, IRA · 2009 to 2025
$11.5M
Signaling Mechanisms of EphrinB1 in Cell Adhesion, Migration and InvasionZ01BC010958 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI DAAR, IRA · 2008 to 2008
$589k
Intramural NIH HHS Z01 BC010958
6 · The paper itself

Abstract

Eph receptors and their corresponding ephrin ligands have been associated with regulating cell-cell adhesion and motility, and thus have a critical role in various biological processes including tissue morphogenesis and homeostasis, as well as pathogenesis of several diseases. Aberrant regulation of Eph/ephrin signaling pathways is implicated in tumor progression of various human cancers. Here, we show that a Rho family GTPase regulator, Rho guanine nucleotide dissociation inhibitor 1 (RhoGDI1), can interact with ephrinB1, and this interaction is enhanced upon binding the extracellular domain of the cognate EphB2 receptor. Deletion mutagenesis revealed that amino acids 327-334 of the ephrinB1 intracellular domain are critical for the interaction with RhoGDI1. Stimulation with an EphB2 extracellular domain-Fc fusion protein (EphB2-Fc) induces RhoA activation and enhances the motility as well as invasiveness of wild-type ephrinB1-expressing cells. These Eph-Fc-induced effects were markedly diminished in cells expressing the mutant ephrinB1 construct (Δ327-334) that is ineffective at interacting with RhoGDI1. Furthermore, ephrinB1 depletion by siRNA suppresses EphB2-Fc-induced RhoA activation, and reduces motility and invasiveness of the SW480 and Hs578T human cancer cell lines. Our study connects the interaction between RhoGDI1 and ephrinB1 to the promotion of cancer cell behavior associated with tumor progression. This interaction may represent a therapeutic target in cancers that express ephrinB1.

Indexed as

Cell MovementApoptosisBiomarkers, TumorCell ProliferationHumansNeoplasm InvasivenessNeoplasmsReceptor, EphB2rhoA GTP-Binding Proteinrho Guanine Nucleotide Dissociation Inhibitor alphaTumor Cells, CulturedBiomarkers, TumorEPHB2 protein, humanReceptor, EphB2rhoA GTP-Binding ProteinRHOA protein, humanrho Guanine Nucleotide Dissociation Inhibitor alpha

Identifiers

PMID29059157
PMCPMC5814325
OpenAlexW2765129331

What Socratic holds

Textmetadata
LicenceCC BY
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.