Evidence map›Paper›PMID 35053440›Full record

ArticleCancers2022

Canine Oral Melanoma Genomic and Transcriptomic Study Defines Two Molecular Subgroups with Different Therapeutical Targets.

Anais Prouteau, Stephanie Mottier, Aline Primot, Edouard Cadieu, Laura Bachelot, Nadine Botherel, Florian Cabillic, Armel Houel, Laurence Cornevin, Camille Kergal and 8 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.5field-weighted citation impact, top 6% 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

20 citing papers in PubMed, 26 citations in OpenAlex.

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  20. The Role of TRPM7 in Oncogenesis.International journal of molecular sciences · 2024
    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

18 authors at 4 institutions in 3 countries.

Anais ProuteauIGDR-UMR 6290, CNRS, University of Rennes 1, 35000 Rennes, France.
Stephanie MottierIGDR-UMR 6290, CNRS, University of Rennes 1, 35000 Rennes, France.
Aline PrimotIGDR-UMR 6290, CNRS, University of Rennes 1, 35000 Rennes, France.
Edouard CadieuIGDR-UMR 6290, CNRS, University of Rennes 1, 35000 Rennes, France.
Laura BachelotIGDR-UMR 6290, CNRS, University of Rennes 1, 35000 Rennes, France.
Nadine BotherelIGDR-UMR 6290, CNRS, University of Rennes 1, 35000 Rennes, France.
Florian CabillicLaboratoire de Cytogénétique et Biologie Cellulaire, CHU de Rennes, INSERM, INRA, University of Rennes 1, Nutrition Metabolisms and Cancer, 35000 Rennes, France.
Armel HouelIGDR-UMR 6290, CNRS, University of Rennes 1, 35000 Rennes, France.
Laurence CornevinLaboratoire de Cytogénétique et Biologie Cellulaire, CHU de Rennes, INSERM, INRA, University of Rennes 1, Nutrition Metabolisms and Cancer, 35000 Rennes, France.
Camille KergalIGDR-UMR 6290, CNRS, University of Rennes 1, 35000 Rennes, France.
Sébastien CorreIGDR-UMR 6290, CNRS, University of Rennes 1, 35000 Rennes, France.ORCID 0000-0003-1532-5660
Jérôme AbadieLaboniris, Department of Biology, Pathology and Food Sciences, Oniris, 44300 Nantes, France.ORCID 0000-0002-7750-0519
Christophe HitteIGDR-UMR 6290, CNRS, University of Rennes 1, 35000 Rennes, France.ORCID 0000-0003-1714-437X
David GilotIGDR-UMR 6290, CNRS, University of Rennes 1, 35000 Rennes, France.ORCID 0000-0002-2646-671X
Kerstin Lindblad-TohBroad Institute of MIT and Harvard, Cambridge, MA 02142, USA.
Catherine AndréIGDR-UMR 6290, CNRS, University of Rennes 1, 35000 Rennes, France.
Thomas DerrienIGDR-UMR 6290, CNRS, University of Rennes 1, 35000 Rennes, France.ORCID 0000-0002-8211-5789
Benoit HedanIGDR-UMR 6290, CNRS, University of Rennes 1, 35000 Rennes, France.ORCID 0000-0002-2418-1868
Centre National de la Recherche Scientifique · FRInserm · FRBroad Institute · USOniris · FR

Funding

Agence Nationale de la Recherche ANR-11-INBS-0003Aviesan/INSERM MTS 2012-08. French Plan Cancer 2009-2013
6 · The paper itself

Abstract

Mucosal melanoma (MM) is a rare, aggressive clinical cancer. Despite recent advances in genetics and treatment, the prognosis of MM remains poor. Canine MM offers a relevant spontaneous and immunocompetent model to decipher the genetic bases and explore treatments for MM. We performed an integrative genomic and transcriptomic analysis of 32 canine MM samples, which identified two molecular subgroups with a different microenvironment and structural variant (SV) content. The overexpression of genes related to the microenvironment and T-cell response was associated with tumors harboring a lower content of SVs, whereas the overexpression of pigmentation-related pathways and oncogenes, such as

Indexed as

CDK4chromosomal rearrangementsdog modelimmune checkpoint inhibitorsMDM2mucosal melanomaoncogenes

Identifiers

PMID35053440
PMCPMC8774001
OpenAlexW4225397005

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.