Evidence map›Paper›PMID 32331328›Full record

ReviewInternational journal of molecular sciences2020

Multiple Sclerosis Treatment and Melanoma Development.

Maria Luigia Carbone, Pedro Miguel Lacal, Serena Messinese, Laura De Giglio, Carlo Pozzilli, Severino Persechino, Cinzia Mazzanti, Cristina Maria Failla, Gianluca Pagnanelli

Open access · goldAbstract readCase ReportsReview
In one paragraph

Review in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

7 citing papers in PubMed, 24 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 4 institutions in 1 country.

Maria Luigia CarboneLaboratory of Experimental Immunology, IDI-IRCCS, 00167 Rome, Italy.
Pedro Miguel LacalLaboratory of Molecular Oncology, IDI-IRCCS, 00167 Rome, Italy.ORCID 0000-0003-1166-4593
Serena MessineseI Dermatology Department, IDI-IRCCS, 00167 Rome, Italy.
Laura De GiglioMedicine Department, Neurology Unit, San Filippo Neri Hospital, 00135 Rome, Italy.
Carlo PozzilliDepartment of Human Neurosciences, Sant'Andrea Hospital, MS Centre, Sapienza University, 00189 Rome, Italy.
Severino PersechinoNESMOS Department, Dermatology Unit, Sant'Andrea Hospital, Sapienza University, 00189 Rome, Italy.
Cinzia MazzantiI Dermatology Department, IDI-IRCCS, 00167 Rome, Italy.
Cristina Maria FaillaLaboratory of Experimental Immunology, IDI-IRCCS, 00167 Rome, Italy.ORCID 0000-0001-5991-8914
Gianluca PagnanelliI Dermatology Department, IDI-IRCCS, 00167 Rome, Italy.
Istituto Dermopatico dell'Immacolata · ITAzienda Ospedaliera Sant'Andrea · ITIstituti di Ricovero e Cura a Carattere Scientifico · ITOspedale San Filippo Neri · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Therapy of multiple sclerosis (MS) with disease-modifying agents such as natalizumab or fingolimod has been associated with the development of cutaneous melanoma. Here we briefly revise literature data and report of a case of a 48-year old woman who developed a melanoma and several atypical naevi after sub sequential treatment with natalizumab (1 year) and fingolimod (7 years). By immunohistochemistry we observed the presence of T cells and leukocyte infiltration as well as of vascular endothelial growth factor (VEGF)-A expression in the patient melanoma biopsy. Then, we analyzed proliferation, migration and VEGF-A expression in three melanoma cell lines and found out that both natalizumab and fingolimod inhibited tumor cell proliferation but promoted or blocked cell migration depending on the cell line examined. VEGF-A secretion was augmented in one melanoma cell line only after fingolimod treatment. In conclusion, our in vitro data do not support the hypothesis of a direct action of natalizumab or fingolimod on melanoma progression but acting on the tumor microenvironment these treatments could indirectly favor melanoma evolution.

Indexed as

Antirheumatic AgentsBiomarkersBiopsyCutaneous Malignant MelanomaDisease SusceptibilityFemaleFingolimod HydrochlorideHumansImmunohistochemistryImmunosuppressive AgentsMelanomaMiddle AgedMultiple SclerosisNatalizumabSkin NeoplasmsVascular Endothelial Growth Factor AAntirheumatic AgentsBiomarkersFingolimod HydrochlorideImmunosuppressive AgentsNatalizumabVascular Endothelial Growth Factor AVEGFA protein, humanfingolimodmelanomanatalizumabVEGF-A

Identifiers

PMID32331328
PMCPMC7216218
OpenAlexW3019503863

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.