Evidence map›Paper›PMID 29534457›Full record

ReviewInternational journal of molecular sciences2018

Strengths and Weaknesses of Pre-Clinical Models for Human Melanoma Treatment: Dawn of Dogs' Revolution for Immunotherapy.

Giuseppina Barutello, Valeria Rolih, Maddalena Arigoni, Lidia Tarone, Laura Conti, Elena Quaglino, Paolo Buracco, Federica Cavallo, Federica Riccardo

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
1.9field-weighted citation impact, top 14% 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, 45 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

9 authors at 2 institutions in 1 country.

Giuseppina BarutelloDepartment of Molecular Biotechnology and Health Sciences, University of Torino, 10126 Torino, Italy. giuseppina.barutello@unito.it.
Valeria RolihDepartment of Molecular Biotechnology and Health Sciences, University of Torino, 10126 Torino, Italy. valeria.rolih@unito.it.
Maddalena ArigoniDepartment of Molecular Biotechnology and Health Sciences, University of Torino, 10126 Torino, Italy. maddalena.arigoni@unito.it.
Lidia TaroneDepartment of Molecular Biotechnology and Health Sciences, University of Torino, 10126 Torino, Italy. lidia.tarone@edu.unito.it.
Laura ContiDepartment of Molecular Biotechnology and Health Sciences, University of Torino, 10126 Torino, Italy. laura.conti@unito.it.
Elena QuaglinoDepartment of Molecular Biotechnology and Health Sciences, University of Torino, 10126 Torino, Italy. elena.quaglino@unito.it.ORCID 0000-0002-8151-9124
Paolo BuraccoDepartment of Veterinary Science, University of Torino, 10095 Grugliasco, Italy. paolo.buracco@unito.it.ORCID 0000-0002-0181-0887
Federica CavalloDepartment of Molecular Biotechnology and Health Sciences, University of Torino, 10126 Torino, Italy. federica.cavallo@unito.it.ORCID 0000-0003-4571-1060
Federica RiccardoDepartment of Molecular Biotechnology and Health Sciences, University of Torino, 10126 Torino, Italy. federica.riccardo@unito.it.ORCID 0000-0002-9692-0172
University of Turin · ITBitron (Italy) · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite several therapeutic advances, malignant melanoma still remains a fatal disease for which novel and long-term curative treatments are needed. The successful development of innovative therapies strongly depends on the availability of appropriate pre-clinical models. For this purpose, several mouse models holding the promise to provide insight into molecular biology and clinical behavior of melanoma have been generated. The most relevant ones and their contribution for the advancement of therapeutic approaches for the treatment of human melanoma patients will be here summarized. However, as models, mice do not recapitulate all the features of human melanoma, thus their strengths and weaknesses need to be carefully identified and considered for the translation of the results into the human clinics. In this panorama, the concept of comparative oncology acquires a priceless value. The revolutionary importance of spontaneous canine melanoma as a translational model for the pre-clinical investigation of melanoma progression and treatment will be here discussed, with a special consideration to the development of innovative immunotherapeutic approaches.

Indexed as

Disease Models, AnimalAnimalsDog DiseasesDogsDrug Evaluation, PreclinicalHumansImmunotherapyMelanomaMicecanine melanomacomparative oncologyCSPG4immunotherapymelanomapre-clinical models

Identifiers

PMID29534457
PMCPMC5877660
OpenAlexW2790657166

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.