Multiple Sclerosis Treatment and Melanoma Development.
Antirheumatic Agents
/ adverse effects
Biomarkers
Biopsy
Disease Susceptibility
Female
Fingolimod Hydrochloride
/ adverse effects
Humans
Immunohistochemistry
Immunosuppressive Agents
/ adverse effects
Melanoma
/ diagnosis
Middle Aged
Multiple Sclerosis
/ complications
Natalizumab
/ adverse effects
Skin Neoplasms
/ diagnosis
Vascular Endothelial Growth Factor A
/ metabolism
Melanoma, Cutaneous Malignant
VEGF-A
fingolimod
melanoma
natalizumab
Journal
International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791
Informations de publication
Date de publication:
22 Apr 2020
22 Apr 2020
Historique:
received:
23
03
2020
revised:
19
04
2020
accepted:
20
04
2020
entrez:
26
4
2020
pubmed:
26
4
2020
medline:
26
1
2021
Statut:
epublish
Résumé
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.
Identifiants
pubmed: 32331328
pii: ijms21082950
doi: 10.3390/ijms21082950
pmc: PMC7216218
pii:
doi:
Substances chimiques
Antirheumatic Agents
0
Biomarkers
0
Immunosuppressive Agents
0
Natalizumab
0
VEGFA protein, human
0
Vascular Endothelial Growth Factor A
0
Fingolimod Hydrochloride
G926EC510T
Types de publication
Case Reports
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Références
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