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@ARTICLE{Gambichler:212426,
author = {T. Gambichler and L. G. Brüggestrat and M. Skrygan and C.
H. Scheel and L. Susok and J. Becker$^*$},
title = {{T}he {A}ntineoplastic {E}ffect of {D}imethyl {F}umarate on
{V}irus-{N}egative {M}erkel {C}ell {C}arcinoma {C}ell
{L}ines: {P}reliminary {R}esults.},
journal = {Cancers},
volume = {15},
number = {2},
issn = {2072-6694},
address = {Basel},
publisher = {MDPI},
reportid = {DKFZ-2023-00145},
pages = {547},
year = {2023},
abstract = {Merkel cell carcinoma (MCC) is a rare, difficult-to-treat
skin cancer once immunotherapy has failed. MCC is associated
either with the clonal integration of the Merkel cell
polyomavirus (MCPyV) or mutagenic UV-radiation. Fumaric acid
esters, including dimethyl fumarate (DMF), have been shown
to inhibit cell growth in cutaneous melanoma and lymphoma.
We aimed to explore the effects of DMF on MCPyV-negative MCC
cell lines. Three MCC cell lines (MCC13, MCC14.2, and MCC26)
were treated with different doses of DMF. The cytotoxic
effects and cell proliferation were assessed by the MTT
cytotoxicity assay and BrdU proliferation assay at different
time points. A significant reduction in cell viability and
proliferation were demonstrated for all the cell lines used,
with DMF proving to be effective.},
keywords = {dimethyl fumarate (Other) / fumaric acid esters (Other) /
merkel cell carcinoma (Other) / monomethyl fumarate (Other)},
cin = {ED01},
ddc = {610},
cid = {I:(DE-He78)ED01-20160331},
pnm = {899 - ohne Topic (POF4-899)},
pid = {G:(DE-HGF)POF4-899},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:36672496},
pmc = {pmc:PMC9857057},
doi = {10.3390/cancers15020547},
url = {https://inrepo02.dkfz.de/record/212426},
}