Evidence map›Paper›PMID 29422656›Full record

ArticleNature communications2018

Methylation profiling identifies two subclasses of squamous cell carcinoma related to distinct cells of origin.

Manuel Rodríguez-Paredes, Felix Bormann, Günter Raddatz, Julian Gutekunst, Carlota Lucena-Porcel, Florian Köhler, Elisabeth Wurzer, Katrin Schmidt, Stefan Gallinat, Horst Wenck and 10 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
7.8field-weighted citation impact, top 2% 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

55 citing papers in PubMed, 90 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

20 authors at 4 institutions in 1 country.

Manuel Rodríguez-ParedesDivision of Epigenetics, DKFZ-ZMBH Alliance, German Cancer Research Center, 69120, Heidelberg, Germany.
Felix BormannDivision of Epigenetics, DKFZ-ZMBH Alliance, German Cancer Research Center, 69120, Heidelberg, Germany.
Günter RaddatzDivision of Epigenetics, DKFZ-ZMBH Alliance, German Cancer Research Center, 69120, Heidelberg, Germany.
Julian GutekunstDivision of Epigenetics, DKFZ-ZMBH Alliance, German Cancer Research Center, 69120, Heidelberg, Germany.
Carlota Lucena-PorcelInstitute of Pathology, Heidelberg University, 69120, Heidelberg, Germany.
Florian KöhlerDivision of Epigenetics, DKFZ-ZMBH Alliance, German Cancer Research Center, 69120, Heidelberg, Germany.
Elisabeth WurzerResearch & Development, Beiersdorf AG, 20253, Hamburg, Germany.
Katrin SchmidtResearch & Development, Beiersdorf AG, 20253, Hamburg, Germany.
Stefan GallinatResearch & Development, Beiersdorf AG, 20253, Hamburg, Germany.
Horst WenckResearch & Development, Beiersdorf AG, 20253, Hamburg, Germany.
Joachim Röwert-HuberDepartment of Dermatology, Venereology and Allergy, Charité, University Hospital, 10117, Berlin, Germany.
Evgeniya DenisovaDivision of Applied Bioinformatics, German Cancer Research Center (DKFZ), 69120, Heidelberg, Germany.
Lars FeuerbachDivision of Applied Bioinformatics, German Cancer Research Center (DKFZ), 69120, Heidelberg, Germany.
Jeongbin ParkDivision of Theoretical Bioinformatics, German Cancer Research Center (DKFZ), 69120, Heidelberg, Germany.
Benedikt BrorsDivision of Applied Bioinformatics, German Cancer Research Center (DKFZ), 69120, Heidelberg, Germany.ORCID http://orcid.org/0000-0001-5940-3101
Esther HerpelInstitute of Pathology, Heidelberg University, 69120, Heidelberg, Germany.
Ingo NindlDepartment of Dermatology, Venereology and Allergy, Charité, University Hospital, 10117, Berlin, Germany.
Thomas G HofmannDivision of Epigenetics, DKFZ-ZMBH Alliance, German Cancer Research Center, 69120, Heidelberg, Germany.
Marc WinnefeldResearch & Development, Beiersdorf AG, 20253, Hamburg, Germany.
Frank LykoDivision of Epigenetics, DKFZ-ZMBH Alliance, German Cancer Research Center, 69120, Heidelberg, Germany. f.lyko@dkfz.de.ORCID http://orcid.org/0000-0002-4873-5431
German Cancer Research Center · DEBeiersdorf (Germany) · DECharité - Universitätsmedizin Berlin · DEHeidelberg University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cutaneous squamous cell carcinoma (cSCC) is the second most common skin cancer and usually progresses from a UV-induced precancerous lesion termed actinic keratosis (AK). Despite various efforts to characterize these lesions molecularly, the etiology of AK and its progression to cSCC remain partially understood. Here, we use Infinium MethylationEPIC BeadChips to interrogate the DNA methylation status in healthy, AK and cSCC epidermis samples. Importantly, we show that AK methylation patterns already display classical features of cancer methylomes and are highly similar to cSCC profiles. Further analysis identifies typical features of stem cell methylomes, such as reduced DNA methylation age, non-CpG methylation, and stem cell-related keratin and enhancer methylation patterns. Interestingly, this signature is detected only in half of the samples, while the other half shows patterns more closely related to healthy epidermis. These findings suggest the existence of two subclasses of AK and cSCC emerging from distinct keratinocyte differentiation stages.

Indexed as

Gene Expression Regulation, NeoplasticAdultAgedAged, 80 and overCarcinoma, Squamous CellCase-Control StudiesCell DifferentiationDNA MethylationFemaleHumansKeratinocytesKeratosis, ActinicMaleMiddle AgedSkin NeoplasmsYoung Adult

Identifiers

PMID29422656
PMCPMC5805678
OpenAlexW2807381463

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.