Evidence map›Paper›PMID 34381187›Full record

ArticleModern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc2021

Nodular fasciitis: a comprehensive, time-correlated investigation of 17 cases.

Zoltán Sápi, Zoltán Lippai, Gergő Papp, Lajos Hegyi, Johanna Sápi, Katalin Dezső, Károly Szuhai

Open access · hybridAbstract readComparative Study
In one paragraph

Article in Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
5.4field-weighted citation impact, top 3% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 36 citations in OpenAlex.

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  14. Molecular testing of soft tissue tumors.Diagnostic cytopathology · 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

7 authors at 3 institutions in 2 countries.

Zoltán Sápi *1st Department of Pathology and Experimental Cancer Research, Semmelweis Univesity, Budapest, Hungary. sapi.zoltan.dr@gmail.com.ORCID 0000-0002-2987-2764
Zoltán Lippai *1st Department of Pathology and Experimental Cancer Research, Semmelweis Univesity, Budapest, Hungary.ORCID 0000-0001-9064-2493
Gergő Papp1st Department of Pathology and Experimental Cancer Research, Semmelweis Univesity, Budapest, Hungary.ORCID 0000-0001-5840-2369
Lajos Hegyi1st Department of Pathology and Experimental Cancer Research, Semmelweis Univesity, Budapest, Hungary.ORCID 0000-0002-3035-5297
Johanna SápiResearch and Innovation Center of Óbuda University, Physiological Controls Group, Óbuda University, Budapest, Hungary.ORCID 0000-0002-9072-1965
Katalin Dezső1st Department of Pathology and Experimental Cancer Research, Semmelweis Univesity, Budapest, Hungary.ORCID 0000-0002-4856-0483
Károly SzuhaiDepartment of Cell and Chemical Biology, Leiden University Medical Center, Leiden, the Netherlands.ORCID 0000-0002-1228-4245
Semmelweis University · HULeiden University Medical Center · NLObuda University · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The self-limited nature of nodular fasciitis (NF) is well-known but its precise mechanism has not yet been clarified. We observed that "young" NF (preoperative duration <1 month) consistently contains a higher percentage (~80%) of USP6 break-apart FISH signals than "old" NF (preoperative duration >3 months) (~20%). Thus, we hypothesized that our original observation may reflect a connection with the self-limited nature of NF. Seventeen cases with reliable data concerning the onset were selected, thus approximating the lifetime of each tumor. Besides the USP6 interphase FISH examination, we also checked the most common MYH9-USP6 fusion using RT-PCR. Because of the known pathways of the tumorigenesis of NF, the mRNA level of USP6, TRAIL, IFN-beta, JAK1, STAT1, STAT3, JUN, and CDKN2A was measured using qRT-PCR. Regarding proteins, USP6, p16, p27, TRAIL, and IFN-beta were examined using immunohistochemistry. Targeted gene panel next-generation sequencing (NGS) of three cases was additionally performed. We found a strong negative correlation (p = 0.000) between the lifetime and percentage of USP6 break-apart signals and a strong positive relationship (p = 0.000) between USP6 break-apart signals and mitotic counts. Results of immunostainings, along with qRT-PCR results, favored the previously-suggested USP6-induced negative feedback mechanism through activation of TRAIL and IFN-beta, likely resulting in apoptosis and senescence of tumor cells harboring USP6 fusions. Targeted-NGS resulted in the detection of several variants, but no additional recurrent changes in the pathogenesis of these tumors. We revealed on a cellular level the USP6-induced negative feedback mechanism. In conclusion, we emphasize that in "old" NF, the percentage of USP6 break-apart FISH signals can be as low as 14-27% which can be very important from a differential diagnostic point of view. We emphasize that a careful examination and interpretation of the NGS data is needed before clinical decision-making on treatment.

Indexed as

Gene FusionGene RearrangementAdolescentAdultBiomarkers, TumorChildChild, PreschoolFasciitisFemaleHigh-Throughput Nucleotide SequencingHumansImmunohistochemistryIn Situ Hybridization, FluorescenceMaleMiddle AgedMyofibroblastsBiomarkers, TumorUbiquitin ThiolesteraseUSP6 protein, human

Identifiers

PMID34381187
PMCPMC8592838
OpenAlexW3192799177

What OpenQuestion holds

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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.