Evidence map›Paper›PMID 40715046›Full record

ArticleCell death & disease2025

Direct transdifferentiation of tumorigenic melanoma cells induces tumor cell reversion.

Yiman Wang, Ke Liu, Yuxin Zhang, Daniel Novak, Aniello Federico, Cai Xu, Sandra Horschitz, Marlene Vierthaler, Qian Sun, Nina Wang and 6 more

Abstract read
In one paragraph

Article in Cell death & disease, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

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

16 authors.

Yiman WangSkin Cancer Unit, German Cancer Research Center (DKFZ), Heidelberg, Baden-Württemberg, Germany.ORCID http://orcid.org/0000-0002-0629-2169
Ke LiuSkin Cancer Unit, German Cancer Research Center (DKFZ), Heidelberg, Baden-Württemberg, Germany.
Yuxin ZhangSkin Cancer Unit, German Cancer Research Center (DKFZ), Heidelberg, Baden-Württemberg, Germany.
Daniel NovakSkin Cancer Unit, German Cancer Research Center (DKFZ), Heidelberg, Baden-Württemberg, Germany.
Aniello FedericoSkin Cancer Unit, German Cancer Research Center (DKFZ), Heidelberg, Baden-Württemberg, Germany.
Cai XuRadiooncology/Radiobiology Department, German Cancer Research Center (DKFZ), Heidelberg, Baden-Württemberg, Germany.
Sandra HorschitzDepartment of Translational Brain Research, Central Institute of Mental Health (ZI), University of Heidelberg/Medical Faculty, Mannheim, Germany.
Marlene VierthalerSkin Cancer Unit, German Cancer Research Center (DKFZ), Heidelberg, Baden-Württemberg, Germany.
Qian SunSkin Cancer Unit, German Cancer Research Center (DKFZ), Heidelberg, Baden-Württemberg, Germany.
Nina WangSkin Cancer Unit, German Cancer Research Center (DKFZ), Heidelberg, Baden-Württemberg, Germany.ORCID http://orcid.org/0009-0001-5410-0248
Juliane PoelchenSkin Cancer Unit, German Cancer Research Center (DKFZ), Heidelberg, Baden-Württemberg, Germany.
Tamara SteinfassSkin Cancer Unit, German Cancer Research Center (DKFZ), Heidelberg, Baden-Württemberg, Germany.
Laura HüserSkin Cancer Unit, German Cancer Research Center (DKFZ), Heidelberg, Baden-Württemberg, Germany.ORCID http://orcid.org/0000-0001-7599-8192
Moritz MallCell Fate Engineering and Disease Modeling Group, German Cancer Research Center (DKFZ) and DKFZ-ZMBH Alliance, Heidelberg, Germany.ORCID http://orcid.org/0000-0002-1278-2594
Viktor UmanskySkin Cancer Unit, German Cancer Research Center (DKFZ), Heidelberg, Baden-Württemberg, Germany.ORCID http://orcid.org/0000-0003-0259-1839
Jochen UtikalSkin Cancer Unit, German Cancer Research Center (DKFZ), Heidelberg, Baden-Württemberg, Germany. j.utikal@dkfz.de.ORCID http://orcid.org/0000-0001-5316-0241

Funding

Deutsche Forschungsgemeinschaft (German Research Foundation) 259332240/ RTG 2099Deutsche Forschungsgemeinschaft (German Research Foundation) 676288/ UT 112/1-1
6 · The paper itself

Abstract

Melanoma is an aggressive skin cancer and highly lethal at advanced stages due to its high tumorigenicity and metastatic capacity. Changing the phenotype of cancer cells from one lineage to another, a process called transdifferentiation, leads to tumor cell reversion, which goes along with a drastic reduction of their tumorigenicity. Via ectopic overexpression of four neuronal transcription factors, we transdifferentiated melanoma cells into neuron-like cells expressing neuronal markers and showing a neuron-like morphology. Moreover, the tumorigenic and metastatic potential of transdifferentiated cells in vitro and in vivo was significantly reduced. Transdifferentiated cells were also more sensitive to radiotherapy compared with their parental counterparts. We conclude that transdifferentiation of cancer cells into terminally differentiated neuron-like cells might represent a prospective new therapeutic approach for the treatment of melanoma.

Indexed as

CarcinogenesisCell TransdifferentiationMelanomaSkin NeoplasmsAnimalsCell Line, TumorHumansMiceNeuronsTranscription FactorsTranscription Factors

Identifiers

PMID40715046
PMCPMC12297470

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.