Evidence map›Paper›PMID 35201472›Full record

ArticleDiscover oncology2021

Involvement of transcribed lncRNA uc.291 and SWI/SNF complex in cutaneous squamous cell carcinoma.

M Mancini, A Cappello, R Pecorari, A M Lena, M Montanaro, L Fania, F Ricci, G Di Lella, M C Piro, D Abeni and 4 more

Open access · goldAbstract read
In one paragraph

Article in Discover oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

14 citing papers in PubMed, 19 citations in OpenAlex.

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  11. ZNF750: A Novel Prognostic Biomarker in Metastatic Prostate Cancer.International journal of molecular sciences · 2023
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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

14 authors at 2 institutions in 1 country.

M ManciniIstituto Dermopatico Dell'Immacolata-IRCCS, via dei Monti di Creta 104, 00167, Rome, Italy.ORCID http://orcid.org/0000-0001-5173-4854
A CappelloDepartment of Experimental Medicine, University of Rome "Tor Vergata", via Montpellier 1, 00133, Rome, Italy.ORCID http://orcid.org/0000-0003-0893-445X
R PecorariDepartment of Experimental Medicine, University of Rome "Tor Vergata", via Montpellier 1, 00133, Rome, Italy.ORCID http://orcid.org/0000-0002-9575-6964
A M LenaDepartment of Experimental Medicine, University of Rome "Tor Vergata", via Montpellier 1, 00133, Rome, Italy.ORCID http://orcid.org/0000-0001-6285-9927
M MontanaroDepartment of Experimental Medicine, University of Rome "Tor Vergata", via Montpellier 1, 00133, Rome, Italy.ORCID http://orcid.org/0000-0001-8441-3731
L FaniaIstituto Dermopatico Dell'Immacolata-IRCCS, via dei Monti di Creta 104, 00167, Rome, Italy.ORCID http://orcid.org/0000-0003-4194-932X
F RicciIstituto Dermopatico Dell'Immacolata-IRCCS, via dei Monti di Creta 104, 00167, Rome, Italy.ORCID http://orcid.org/0000-0002-8388-9268
G Di LellaIstituto Dermopatico Dell'Immacolata-IRCCS, via dei Monti di Creta 104, 00167, Rome, Italy.ORCID http://orcid.org/0000-0002-5945-7860
M C PiroDepartment of Experimental Medicine, University of Rome "Tor Vergata", via Montpellier 1, 00133, Rome, Italy.ORCID http://orcid.org/0000-0003-3004-367X
D AbeniIstituto Dermopatico Dell'Immacolata-IRCCS, via dei Monti di Creta 104, 00167, Rome, Italy.ORCID http://orcid.org/0000-0002-0167-7617
E DellambraIstituto Dermopatico Dell'Immacolata-IRCCS, via dei Monti di Creta 104, 00167, Rome, Italy.ORCID http://orcid.org/0000-0002-4329-3312
A MaurielloDepartment of Experimental Medicine, University of Rome "Tor Vergata", via Montpellier 1, 00133, Rome, Italy.ORCID http://orcid.org/0000-0002-7351-5676
G MelinoDepartment of Experimental Medicine, University of Rome "Tor Vergata", via Montpellier 1, 00133, Rome, Italy.ORCID http://orcid.org/0000-0001-9428-5972
E CandiIstituto Dermopatico Dell'Immacolata-IRCCS, via dei Monti di Creta 104, 00167, Rome, Italy. candi@uniorma2.it.ORCID http://orcid.org/0000-0001-8332-4825
University of Rome Tor Vergata · ITIstituto Dermopatico dell'Immacolata · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

While non-melanoma skin cancers (NMSCs) are the most common tumours in humans, only the sub-type cutaneous squamous cell carcinoma (cSCC), might become metastatic with high lethality. We have recently identified a regulatory pathway involving the lncRNA transcript uc.291 in controlling the expression of epidermal differentiation complex genes via the interaction with ACTL6A, a component of the chromatin remodelling complex SWI/SNF. Since transcribed ultra-conserved regions (T-UCRs) are expressed in normal tissues and are deregulated in tumorigenesis, here we hypothesize a potential role for dysregulation of this axis in cSCC, accounting for the de-differentiation process observed in aggressive poorly differentiated cutaneous carcinomas. We therefore analysed their expression patterns in human tumour biopsies at mRNA and protein levels. The results suggest that by altering chromatin accessibility of the epidermal differentiation complex genes, down-regulation of uc.291 and BRG1 expression contribute to the de-differentiation process seen in keratinocyte malignancy. This provides future direction for the identification of clinical biomarkers in cutaneous SCC. Analysis of publicly available data sets indicates that the above may also be a general feature for SCCs of different origins.

Indexed as

ACTL6ABasal cell carcinomaEpidermisLncRNASquamous cell carcinomaSWI/SNF complex

Identifiers

PMID35201472
PMCPMC8777507
OpenAlexW3164852363

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.