Evidence map›Paper›PMID 42658270›Full record

ArticleHistochemistry and cell biology2026

Lamin subtype expression in Merkel-cell carcinoma: its relation to polyomavirus infection and tumor metastasis.

Merel Stiekema, Monique Ummelen, Moritz Jesinghaus, Corinna U Keber, Viktoria Wischmann, Ingrid Moll, Jack Cleutjens, Marc A M J van Zandvoort, Jos L V Broers, Frans C S Ramaekers and 1 more

Abstract read
In one paragraph

Article in Histochemistry and cell biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Merel StiekemaDepartment of Genetics and Cell Biology, Maastricht University Medical Centre, Universiteitssingel 50, 6229ER, Maastricht, The Netherlands. m.stiekema@maastrichtuniversity.nl.ORCID https://orcid.org/0009-0004-4221-7248
Monique UmmelenDepartment of Genetics and Cell Biology, Maastricht University Medical Centre, Universiteitssingel 50, 6229ER, Maastricht, The Netherlands.
Moritz JesinghausInstitute of Pathology, Philipps-Universität Marburg, Marburg, Germany.ORCID http://orcid.org/0000-0002-0018-5661
Corinna U KeberInstitute of Pathology, Philipps-Universität Marburg, Marburg, Germany.ORCID http://orcid.org/0000-0002-4312-1377
Viktoria WischmannInstitute of Pathology, Philipps-Universität Marburg, Marburg, Germany.
Ingrid MollDepartment of Dermatology and Venerology, University Hospital Hamburg-Eppendorf, Hamburg, Germany.ORCID http://orcid.org/0000-0003-4162-8112
Jack CleutjensDepartment of Pathology, Maastricht University Medical Centre, Maastricht, The Netherlands.ORCID http://orcid.org/0000-0002-4346-1785
Marc A M J van ZandvoortDepartment of Genetics and Cell Biology, Maastricht University Medical Centre, Universiteitssingel 50, 6229ER, Maastricht, The Netherlands.ORCID http://orcid.org/0000-0003-0483-6641
Jos L V BroersDepartment of Genetics and Cell Biology, Maastricht University Medical Centre, Universiteitssingel 50, 6229ER, Maastricht, The Netherlands.ORCID https://orcid.org/0000-0002-3724-6982
Frans C S RamaekersDepartment of Genetics and Cell Biology, Maastricht University Medical Centre, Universiteitssingel 50, 6229ER, Maastricht, The Netherlands.ORCID http://orcid.org/0009-0002-1324-5843
Roland MollInstitute of Pathology, Philipps-Universität Marburg, Marburg, Germany.ORCID http://orcid.org/0000-0002-1791-922X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Merkel-cell carcinoma (MCC) is known for its high metastatic potential. Studies in several tumor types have proposed a role for up- or downregulation of nuclear A- and B-type lamins in facilitating the process of invasion and metastasis, but such studies are lacking for MCC. Therefore, lamin expression levels were examined in 38 tissue samples from 28 patients with MCC using immunohistochemistry. The series comprised primary tumors and different metastases and both Merkel cell polyomavirus (MCPyV) positive and MCPyV-negative cases. This study revealed that primary MCC tumors express variable, but mostly low levels of A-type lamins, while the B-type lamins are overall highly expressed. No obvious differences in lamin expression were observed between the MCPyV-positive and MCPyV-negative cases. A generally higher A-type lamin expression was detected in MCC metastases, although comparison of primary tumors versus metastases from the same patients showed either no change or up- or downregulation of A-type lamins. Normal Merkel cells were found to express both A- and B-type lamins. Conclusively, our data suggest a flexible A-type lamin expression in the process of MCC carcinogenesis and metastasis, which is an important finding regarding the aggressiveness of MCC and in the debate about the cellular origin of MCC.

Indexed as

Carcinoma, Merkel CellLaminsPolyomavirus InfectionsSkin NeoplasmsTumor Virus InfectionsAgedAged, 80 and overFemaleHumansImmunohistochemistryMaleMerkel cell polyomavirusMiddle AgedNeoplasm MetastasisLaminsImmunohistochemistryMerkel cellsNuclear lamina

Identifiers

PMID42658270
PMCPMC13522004

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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.