Evidence map›Paper›PMID 32865618›Full record

ArticleJournal of cancer research and clinical oncology2020

UV-type specific alteration of miRNA expression and its association with tumor progression and metastasis in SCC cell lines.

I-Peng Chen, Marc Bender, Ivelina Spassova, Stefan Henning, Linda Kubat, Kaiji Fan, Sarah Degenhardt, Mouna Mhamdi-Ghodbani, Ashwin Sriram, Beate Volkmer and 3 more

Open access · greenAbstract read
In one paragraph

Article in Journal of cancer research and clinical oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.7field-weighted citation impact, top 14% 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

9 citing papers in PubMed, 16 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

13 authors at 2 institutions in 1 country.

I-Peng Chen *Division of Molecular Cell Biology, Skin Cancer Center, Elbe Kliniken Stade-Buxtehude, 21614, Buxtehude, Germany.
Marc Bender *Division of Molecular Cell Biology, Skin Cancer Center, Elbe Kliniken Stade-Buxtehude, 21614, Buxtehude, Germany.
Ivelina SpassovaTranslational Skin Cancer Research, DKTK Partner Site Essen/Düsseldorf, West German Cancer Center, Dermatology, University Duisburg-Essen, 45117, Essen, Germany.
Stefan HenningDivision of Molecular Cell Biology, Skin Cancer Center, Elbe Kliniken Stade-Buxtehude, 21614, Buxtehude, Germany.
Linda KubatTranslational Skin Cancer Research, DKTK Partner Site Essen/Düsseldorf, West German Cancer Center, Dermatology, University Duisburg-Essen, 45117, Essen, Germany.
Kaiji FanTranslational Skin Cancer Research, DKTK Partner Site Essen/Düsseldorf, West German Cancer Center, Dermatology, University Duisburg-Essen, 45117, Essen, Germany.
Sarah DegenhardtDivision of Molecular Cell Biology, Skin Cancer Center, Elbe Kliniken Stade-Buxtehude, 21614, Buxtehude, Germany.
Mouna Mhamdi-GhodbaniDivision of Molecular Cell Biology, Skin Cancer Center, Elbe Kliniken Stade-Buxtehude, 21614, Buxtehude, Germany.
Ashwin SriramTranslational Skin Cancer Research, DKTK Partner Site Essen/Düsseldorf, West German Cancer Center, Dermatology, University Duisburg-Essen, 45117, Essen, Germany.
Beate VolkmerDivision of Molecular Cell Biology, Skin Cancer Center, Elbe Kliniken Stade-Buxtehude, 21614, Buxtehude, Germany.
Petra BoukampDivision of Genetics of Skin Carcinogenesis, German Cancer Research Center, Im Neuenheimer Feld 280, 69120, Heidelberg, Germany.
Jürgen C BeckerTranslational Skin Cancer Research, DKTK Partner Site Essen/Düsseldorf, West German Cancer Center, Dermatology, University Duisburg-Essen, 45117, Essen, Germany.
Rüdiger GreinertDivision of Molecular Cell Biology, Skin Cancer Center, Elbe Kliniken Stade-Buxtehude, 21614, Buxtehude, Germany. ruediger.greinert@elbekliniken.de.ORCID http://orcid.org/0000-0003-3479-9968
Elbe Kliniken Stade-Buxtehude · DEGerman Cancer Research Center · DE

Funding

Bundesministerium für Bildung und Forschung 02NUK036BHiege-Stiftung gegen Hautkrebs D/106-21076
6 · The paper itself

Abstract

purposeUV exposure is the main risk factor for development of cutaneous squamous cell carcinoma (cSCC). While early detection greatly improves cSCC prognosis, locally advanced or metastatic cSCC has a severely impaired prognosis. Notably, the mechanisms of progression to metastatic cSCC are not well understood. We hypothesized that UV exposure of already transformed epithelial cSCC cells further induces changes which might be involved in the progression to metastatic cSCCs and that UV-inducible microRNAs (miRNAs) might play an important role.

methodsThus, we analyzed the impact of UV radiation of different quality (UVA, UVB, UVA + UVB) on the miRNA expression pattern in established cell lines generated from primary and metastatic cSCCs (Met-1, Met-4) using the NanoString nCounter platform.

resultsThis analysis revealed that the expression pattern of miRNAs depends on both the cell line used per se and on the quality of UV radiation. Comparison of UV-induced miRNAs in cSCC cell lines established from a primary tumor (Met-1) and the respective (un-irradiated) metastasis (Met-4) suggest that miR-7-5p, miR-29a-3p and miR-183-5p are involved in a UV-driven pathway of progression to metastasis. This notion is supported by the fact that these three miRNAs build up a network of 81 potential target genes involved e.g. in UVA/UVB-induced MAPK signaling and regulation of the epithelial-mesenchymal transition. As an example, PTEN, a target of UV-upregulated miRNAs (miR-29a-3p, miR-183-5p), could be shown to be down-regulated in response to UV radiation. We further identified CNOT8, the transcription complex subunit 8 of the CCR4-NOT complex, a deadenylase removing the poly(A) tail from miRNA-destabilized mRNAs, in the center of this network, targeted by all three miRNAs.

conclusionIn summary, our results demonstrate that UV radiation induces an miRNA expression pattern in primary SCC cell line partly resembling those of metastatic cell line, thus suggesting that UV radiation impacts SCC progression beyond initiation.

Indexed as

Carcinoma, Squamous CellCell Line, TumorCell ProliferationDisease ProgressionEpithelial-Mesenchymal TransitionGene Expression Regulation, NeoplasticHumansMicroRNAsNeoplasm MetastasisSkin NeoplasmsUltraviolet RaysMicroRNAscSCC cell linesCutaneous squamous cell carcinoma (cSCC)MetastasismiRNAsSkin cancerUV radiation

Identifiers

PMID32865618
PMCPMC11804497
OpenAlexW3082959490

What Socratic holds

Textmetadata
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 Socratic graph.