Evidence map›Paper›PMID 34572907›Full record

ArticleCancers2021

Newly-Discovered Neural Features Expand the Pathobiological Knowledge of Blastic Plasmacytoid Dendritic Cell Neoplasm.

Maria Rosaria Sapienza, Giuseppe Benvenuto, Manuela Ferracin, Saveria Mazzara, Fabio Fuligni, Claudio Tripodo, Beatrice Belmonte, Daniele Fanoni, Federica Melle, Giovanna Motta and 14 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.6field-weighted citation impact, top 36% 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

7 citing papers in PubMed, 8 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

24 authors at 12 institutions in 4 countries.

Maria Rosaria SapienzaDivision of Haematopathology, IEO, European Institute of Oncology IRCCS, 20141 Milan, Italy.ORCID 0000-0002-1078-2128
Giuseppe BenvenutoDepartment of Biology, University of Padua, 35122 Padua, Italy.ORCID 0000-0001-9147-4946
Manuela FerracinDepartment of Experimental, Diagnostic and Specialty Medicine, University of Bologna, 40138 Bologna, Italy.ORCID 0000-0002-1595-6887
Saveria MazzaraDivision of Haematopathology, IEO, European Institute of Oncology IRCCS, 20141 Milan, Italy.
Fabio FuligniDepartment of Genetics and Genome Biology, The Hospital for Sick Children, Toronto, ON M5G 0A4, Canada.
Claudio TripodoTumor Immunology Unit, Human Pathology Section, Department of Health Science, Palermo University School of Medicine, 90134 Palermo, Italy.
Beatrice BelmonteTumor Immunology Unit, Human Pathology Section, Department of Health Science, Palermo University School of Medicine, 90134 Palermo, Italy.ORCID 0000-0001-9668-0925
Daniele FanoniDepartment of Pathophysiology and Transplantation, University of Milan, 20122 Milan, Italy.ORCID 0000-0003-0484-0130
Federica MelleDivision of Haematopathology, IEO, European Institute of Oncology IRCCS, 20141 Milan, Italy.ORCID 0000-0002-5541-2673
Giovanna MottaDivision of Haematopathology, IEO, European Institute of Oncology IRCCS, 20141 Milan, Italy.
Valentina TabanelliDivision of Haematopathology, IEO, European Institute of Oncology IRCCS, 20141 Milan, Italy.
Jessica ConsiglioDepartment of Molecular Virology, Immunology and Medical Genetics, Ohio State University, Columbus, OH 43210, USA.
Vincenzo MazzaraDivision of Haematopathology, IEO, European Institute of Oncology IRCCS, 20141 Milan, Italy.
Marcello Del CorvoDivision of Haematopathology, IEO, European Institute of Oncology IRCCS, 20141 Milan, Italy.
Stefano FioriDivision of Haematopathology, IEO, European Institute of Oncology IRCCS, 20141 Milan, Italy.
Alessandro PileriDepartment of Experimental, Diagnostic and Specialty Medicine, University of Bologna, 40138 Bologna, Italy.
Gaetano Ivan DellinoDepartment of Experimental Oncology, European Institute of Oncology, 20141 Milan, Italy.
Lorenzo CerroniDie Dermatopathologie der Universitätsklinik für Dermatologie und Venerologie, LKH-Univ. Klinikum Graz, 8036 Graz, Austria.
Fabio FacchettiPathology Section, Department of Molecular and Translational Medicine, University of Brescia, 25123 Brescia, Italy.
Emilio BertiDepartment of Pathophysiology and Transplantation, University of Milan, 20122 Milan, Italy.
Elena SabattiniHaematopathology Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, 40138 Bologna, Italy.ORCID 0000-0002-4136-3591
Marco PaulliUnit of Anatomic Pathology, Department of Molecular Medicine, University of Pavia and Fondazione IRCCS San Matteo Polyclinic, 27100 Pavia, Italy.
Carlo Maria CroceDepartment of Molecular Virology, Immunology and Medical Genetics, Ohio State University, Columbus, OH 43210, USA.
Stefano A PileriDivision of Haematopathology, IEO, European Institute of Oncology IRCCS, 20141 Milan, Italy.ORCID 0000-0001-8032-5128
Istituti di Ricovero e Cura a Carattere Scientifico · ITThe Ohio State University · USUniversity of Bologna · ITUniversity of Milan · ITUniversity of Palermo · ITAzienda USL di Bologna · ITEuropean Institute of Oncology · ITGraz University Hospital · ATHospital for Sick Children · CAUniversity of Brescia · ITUniversity of Padua · ITUniversity of Pavia · IT

Funding

Associazione Italiana per la Ricerca sul Cancro 21198
6 · The paper itself

Abstract

Blastic plasmacytoid dendritic cell neoplasm (BPDCN) is a rare and highly aggressive hematologic malignancy originating from plasmacytoid dendritic cells (pDCs). The microRNA expression profile of BPDCN was compared to that of normal pDCs and the impact of miRNA dysregulation on the BPDCN transcriptional program was assessed. MiRNA and gene expression profiling data were integrated to obtain the BPDCN miRNA-regulatory network. The biological process mainly dysregulated by this network was predicted to be neurogenesis, a phenomenon raising growing interest in solid tumors. Neurogenesis was explored in BPDCN by querying different molecular sources (RNA sequencing, Chromatin immunoprecipitation-sequencing, and immunohistochemistry). It was shown that BPDCN cells upregulated neural mitogen genes possibly critical for tumor dissemination, expressed neuronal progenitor markers involved in cell migration, exchanged acetylcholine neurotransmitter, and overexpressed multiple neural receptors that may stimulate tumor proliferation, migration and cross-talk with the nervous system. Most neural genes upregulated in BPDCN are currently investigated as therapeutic targets.

Indexed as

BPDCNmiRNAnetworkneurogenesissequencing

Identifiers

PMID34572907
PMCPMC8469149
OpenAlexW3201647090

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.