Evidence map›Paper›PMID 31248212›Full record

ArticleCancers2019

Myoferlin Contributes to the Metastatic Phenotype of Pancreatic Cancer Cells by Enhancing Their Migratory Capacity through the Control of Oxidative Phosphorylation.

Gilles Rademaker, Brunella Costanza, Sandy Anania, Ferman Agirman, Naïma Maloujahmoum, Emmanuel Di Valentin, Jean Jacques Goval, Akeila Bellahcène, Vincenzo Castronovo, Olivier Peulen

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 2 pooled it
2.0field-weighted citation impact, top 12% 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

25 citing papers in PubMed, 2 syntheses or guidelines pooled it, 32 citations in OpenAlex.

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  16. Cancer cell metabolic plasticity in migration and metastasis.Clinical & experimental metastasis · 2021
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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

10 authors at 1 institution in 1 country.

Gilles RademakerMetastasis Research Laboratory, Giga Cancer, University of Liège, 4000 Liège, Belgium. g.rademaker@uliege.be.ORCID 0000-0003-0170-781X
Brunella CostanzaMetastasis Research Laboratory, Giga Cancer, University of Liège, 4000 Liège, Belgium. brunellacostanza@gmail.com.ORCID 0000-0001-8279-805X
Sandy AnaniaMetastasis Research Laboratory, Giga Cancer, University of Liège, 4000 Liège, Belgium. sandy.anania@uliege.be.
Ferman AgirmanMetastasis Research Laboratory, Giga Cancer, University of Liège, 4000 Liège, Belgium. f.agirman@uliege.be.
Naïma MaloujahmoumMetastasis Research Laboratory, Giga Cancer, University of Liège, 4000 Liège, Belgium. naima.maloujahmoum@uliege.be.
Emmanuel Di ValentinViral Vector Platform, Giga Research, University of Liège, 4000 Liège, Belgium. edivalentin@uliege.be.
Jean Jacques GovalImaging Platform, Giga Research, University of Liège, 4000 Liège, Belgium. jean-jacques.goval@uliege.be.
Akeila BellahcèneMetastasis Research Laboratory, Giga Cancer, University of Liège, 4000 Liège, Belgium. a.bellahcene@uliege.be.ORCID 0000-0001-9154-7631
Vincenzo CastronovoMetastasis Research Laboratory, Giga Cancer, University of Liège, 4000 Liège, Belgium. vcastronovo@uliege.be.
Olivier PeulenMetastasis Research Laboratory, Giga Cancer, University of Liège, 4000 Liège, Belgium. olivier.peulen@uliege.be.ORCID 0000-0002-6933-0134
University of Liège · BE

Funding

Fonds Léon Fredericq 20181071Patrimoine de L'Université de Liège FSR-S-SS-18/10
6 · The paper itself

Abstract

Pancreatic ductal adenocarcinoma (PDAC) is one of the deadliest malignancies with an overall survival of 5% and is the second cause of death by cancer, mainly linked to its high metastatic aggressiveness. Accordingly, understanding the mechanisms sustaining the PDAC metastatic phenotype remains a priority. In this study, we generated and used a murine in vivo model to select clones from the human Panc-1 PDAC cell line that exhibit a high propensity to seed and metastasize into the liver. We showed that myoferlin, a protein previously reported to be overexpressed in PDAC, is significantly involved in the migratory abilities of the selected cells. We first report that highly metastatic Panc-1 clones expressed a significantly higher myoferlin level than the corresponding low metastatic ones. Using scratch wound and Boyden's chamber assays, we show that cells expressing a high myoferlin level have higher migratory potential than cells characterized by a low myoferlin abundance. Moreover, we demonstrate that myoferlin silencing leads to a migration decrease associated with a reduction of mitochondrial respiration. Since mitochondrial oxidative phosphorylation has been shown to be implicated in the tumor progression and dissemination, our data identify myoferlin as a valid potential therapeutic target in PDAC.

Indexed as

metastasismitochondriamyoferlinoxidative phosphorylationpancreas cancer

Identifiers

PMID31248212
PMCPMC6628295
OpenAlexW2952319521

What OpenQuestion 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 OpenQuestion graph.