Evidence map›Paper›PMID 27065325›Full record

ArticleOncogene2016

Targeting soluble CD146 with a neutralizing antibody inhibits vascularization, growth and survival of CD146-positive tumors.

J Stalin, M Nollet, P Garigue, S Fernandez, L Vivancos, A Essaadi, A Muller, R Bachelier, A Foucault-Bertaud, L Fugazza and 5 more

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
3.5field-weighted citation impact, top 8% 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

32 citing papers in PubMed, 62 citations in OpenAlex.

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  17. Comparison of a NewCells · 2021
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  20. Cell Adhesion Molecules in Plasticity and Metastasis.Molecular cancer research : MCR · 2021
    Review
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 2 institutions in 1 country.

J StalinINSERM UMR-S 1076, Aix-Marseille University, UFR Pharmacy, Marseille, France.
M NolletINSERM UMR-S 1076, Aix-Marseille University, UFR Pharmacy, Marseille, France.
P GarigueINSERM UMR-S 1076, Aix-Marseille University, UFR Pharmacy, Marseille, France.
S FernandezCERIMED (European Center of Research in Medical Imaging), Aix-Marseille University, Marseille, France.
L VivancosINSERM UMR-S 1076, Aix-Marseille University, UFR Pharmacy, Marseille, France.
A EssaadiINSERM UMR-S 1076, Aix-Marseille University, UFR Pharmacy, Marseille, France.
A MullerINSERM UMR-S 1076, Aix-Marseille University, UFR Pharmacy, Marseille, France.
R BachelierINSERM UMR-S 1076, Aix-Marseille University, UFR Pharmacy, Marseille, France.
A Foucault-BertaudINSERM UMR-S 1076, Aix-Marseille University, UFR Pharmacy, Marseille, France.
L FugazzaAdvanced Accelerator Applications SRL, Colleretto Giacosa (TO), Italy.
A S LeroyerINSERM UMR-S 1076, Aix-Marseille University, UFR Pharmacy, Marseille, France.
N BardinINSERM UMR-S 1076, Aix-Marseille University, UFR Pharmacy, Marseille, France.
B GuilletINSERM UMR-S 1076, Aix-Marseille University, UFR Pharmacy, Marseille, France.
F Dignat-GeorgeINSERM UMR-S 1076, Aix-Marseille University, UFR Pharmacy, Marseille, France.
M Blot-ChabaudINSERM UMR-S 1076, Aix-Marseille University, UFR Pharmacy, Marseille, France.
Aix-Marseille Université · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CD146 (MUC-18, MCAM) expression on cancer cells correlates with cancer progression and a bad prognosis in several tumors, including melanoma and pancreatic tumors. Deciphering the mechanism mediating the CD146 role in cancer is essential for generating new therapeutic strategies. We found that CD146 expression in cancer cells is associated with a secretion of soluble CD146 (sCD146) that constitutes an active player in tumor development. Indeed, sCD146 induces the overexpression of its binding protein, angiomotin, on both endothelial and cancer cells and promotes both paracrine effects on angiogenesis and autocrine effects on cancer cells proliferation and survival. These last effects are mediated in part through the induction and phosphorylation of c-myc in cancer cells. In mice models xenografted with human CD146-positive melanoma or pancreatic cancer cells, administration of a novel monoclonal antibody specifically targeting sCD146, but not its membrane form, successfully suppresses tumor vascularization and growth. Our findings demonstrate that sCD146 secreted by CD146-positive tumors mediates important pro-angiogenic and pro-tumoral effects. Targeting sCD146 with a novel neutralizing antibody could thus constitute an innovative therapeutic strategy for the treatment of CD146-positive tumors.

Indexed as

AngiomotinsAnimalsAntibodies, MonoclonalAntibodies, NeutralizingApoptosisBiomarkersCD146 AntigenCell Line, TumorCell ProliferationCell SurvivalDisease Models, AnimalEndothelial CellsHumansIntercellular Signaling Peptides and ProteinsMaleMembrane ProteinsAMOT protein, humanAngiomotinsAntibodies, MonoclonalAntibodies, NeutralizingBiomarkersCD146 AntigenIntercellular Signaling Peptides and ProteinsMembrane ProteinsMicrofilament Proteins

Identifiers

PMID27065325
OpenAlexW2333971940

What OpenQuestion holds

Textmetadata
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.