Evidence map›Paper›PMID 28073170›Full record

ArticleInternational journal of cancer2017

Loss of hSef promotes metastasis through upregulation of EMT in prostate cancer.

Satoshi Hori, Karan Wadhwa, Venkat Pisupati, Vincent Zecchini, Antonio Ramos-Montoya, Anne Y Warren, David E Neal, Vincent J Gnanapragasam

Open access · hybridAbstract read
In one paragraph

Article in International journal of cancer, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

11 citing papers in PubMed, 28 citations in OpenAlex.

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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

8 authors at 4 institutions in 3 countries.

Satoshi HoriAcademic Urology Group, Department of Surgery, University of Cambridge, Cambridge, United Kingdom.
Karan WadhwaAcademic Urology Group, Department of Surgery, University of Cambridge, Cambridge, United Kingdom.
Venkat PisupatiAcademic Urology Group, Department of Surgery, University of Cambridge, Cambridge, United Kingdom.
Vincent ZecchiniUro-oncology Group, Cancer Research UK Cambridge Institute, Cambridge, United Kingdom.
Antonio Ramos-MontoyaUro-oncology Group, Cancer Research UK Cambridge Institute, Cambridge, United Kingdom.
Anne Y WarrenDepartment of Pathology, Addenbrooke's Hospital, Cambridge, United Kingdom.
David E NealUro-oncology Group, Cancer Research UK Cambridge Institute, Cambridge, United Kingdom.
Vincent J GnanapragasamAcademic Urology Group, Department of Surgery, University of Cambridge, Cambridge, United Kingdom.
Cancer Research UK Cambridge Center · GBBridge University · SSAddenbrooke's Hospital · GBUniversity of Cambridge · GB

Funding

Medical Research Council G1001961
6 · The paper itself

Abstract

We have previously reported that the negative signaling regulator Similar Expression to FGF (hSef) is downregulated in prostate cancer and its loss is associated with clinical metastasis. Here, we explored the mechanistic basis of this finding. We first confirmed our clinical observation by testing hSef manipulation in an in vivo metastasis model. hSef stable expressing cells (PC3M-hSef) or empty vector controls (PC3M-EV) were injected subcutaneously into the lateral thoracic walls of NOD-SCID gamma mice and lungs were harvested at autopsy. In this model, 6/7 PC3M-EV xenografts had definitive lung micro-metastasis whilst only 1/6 PC3M-hSef xenografts exhibited metastasis recapitulating the clinical scenario (p = 0.03). Gene expression studies revealed key perturbations in genes involved in cell motility and epithelial to mesenchymal transition (EMT) along with alterations in cognate signaling pathways. These results were validated in an EMT specific PCR array whereby hSef over-expression and silencing reciprocally altered E-Cadherin expression (p = <0.001) amongst other EMT markers. Immunohistochemistry of excised tumors from the xenografts also confirmed the effect of hSef in suppressing E-Cadherin expression at the protein level. Phosphokinase arrays further demonstrated a role for hSef in attenuating signaling of not only ERK-MAPK but also the JNK and p38 pathways as well. Taken together, these data suggest evidence that loss of hSef may be a critical event facilitating tumor dissemination of prostate cancer through alteration of EMT. Detection of downregulated hSef, along with other negative regulators, may therefore be a useful biomarker heralding a transition to a metastatic phenotype and warrants further exploration in this context.

Indexed as

AnimalsAntigens, CDBiomarkers, TumorCadherinsCell Line, TumorEpithelial-Mesenchymal TransitionGene Expression Regulation, NeoplasticHumansMaleMAP Kinase Signaling SystemMiceNeoplasm Metastasisp38 Mitogen-Activated Protein KinasesProstatic NeoplasmsReceptors, InterleukinXenograft Model Antitumor AssaysAntigens, CDBiomarkers, TumorCadherinsCDH1 protein, humanIL17RD protein, humanp38 Mitogen-Activated Protein KinasesReceptors, InterleukinEMTmetastasisnegative regulatorprostate cancerSef

Identifiers

PMID28073170
PMCPMC5324539
OpenAlexW2570083968

What OpenQuestion holds

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LicenceCC BY
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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.