Evidence map›Paper›PMID 37381763›Full record

ArticleHaematologica2023

Long non-coding RNA mitophagy and ALK-negative anaplastic lymphoma-associated transcript: a novel regulator of mitophagy in T-cell lymphoma.

Valentina Mularoni, Benedetta Donati, Annalisa Tameni, Veronica Manicardi, Francesca Reggiani, Elisabetta Sauta, Magda Zanelli, Marco Tigano, Emanuele Vitale, Federica Torricelli and 13 more

Open access · goldAbstract read
In one paragraph

Article in Haematologica, 2023. 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
1.9field-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

7 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Programmed Death Ligand 1 (PD-L1) Expression in Lymphomas: State of the Art.International journal of molecular sciences · 2024
    Review
  7. Review
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

23 authors at 8 institutions in 2 countries.

Valentina MularoniLaboratory of Translational Research, Azienda USL-IRCCS di Reggio Emilia, Viale Risorgimento 80, 42123, Reggio Emilia.
Benedetta DonatiLaboratory of Translational Research, Azienda USL-IRCCS di Reggio Emilia, Viale Risorgimento 80, 42123, Reggio Emilia.
Annalisa TameniLaboratory of Translational Research, Azienda USL-IRCCS di Reggio Emilia, Viale Risorgimento 80, 42123, Reggio Emilia.
Veronica ManicardiLaboratory of Translational Research, Azienda USL-IRCCS di Reggio Emilia, Viale Risorgimento 80, 42123, Reggio Emilia.
Francesca ReggianiLaboratory of Translational Research, Azienda USL-IRCCS di Reggio Emilia, Viale Risorgimento 80, 42123, Reggio Emilia.
Elisabetta SautaIRCCS Humanitas Clinical and Research Center, via Manzoni 56, 20089, Rozzano, Milan.
Magda ZanelliPathology Unit, Department of Oncology, Azienda Unità Sanitaria Locale - IRCCS di Reggio Emilia, Reggio Emilia, 42123.
Marco TiganoSidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, PA, 19144.
Emanuele VitaleLaboratory of Translational Research, Azienda USL-IRCCS di Reggio Emilia, Viale Risorgimento 80, 42123, Reggio Emilia, Italy; Clinical and Experimental Medicine Ph.D. Program, University of Modena and Reggio Emilia, Modena, 41125.
Federica TorricelliLaboratory of Translational Research, Azienda USL-IRCCS di Reggio Emilia, Viale Risorgimento 80, 42123, Reggio Emilia.
Stefano AscaniPathology Unit, Azienda Ospedaliera Santa Maria di Terni, University of Perugia, 05100 Terni.
Giovanni MartinoPathology Unit, Azienda Ospedaliera Santa Maria di Terni, University of Perugia, 05100 Terni, Italy; Institute of Hematology and CREO, University of Perugia, Perugia 06129.
Giorgio InghiramiDepartment of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, NY, 10065.
Francesca SanguedolcePathology Unit, Policlinico Riuniti, University of Foggia, 71122 Foggia.
Alessia RuffiniHematology Unit, Azienda USL-IRCCS di Reggio Emilia, 42123 Reggio Emilia.
Alberto BavieriHematology Unit, Azienda USL-IRCCS di Reggio Emilia, 42123 Reggio Emilia.
Stefano LuminariHematology Unit, Azienda USL-IRCCS di Reggio Emilia, 42123 Reggio Emilia.
Marco PizziSurgical Pathology and Cytopathology Unit, Department of Medicine-DIMED, University of Padova, 35128 Padova.
Angelo Paolo Dei TosSurgical Pathology and Cytopathology Unit, Department of Medicine-DIMED, University of Padova, 35128 Padova.
Cinzia FesceHematology Unit, University Hospital, 71122 Foggia.
Antonino NeriScientific Directorate, Azienda USL-IRCCS di Reggio Emilia, Viale Umberto I 50, 42123, Reggio Emilia.
Alessia CiarrocchiLaboratory of Translational Research, Azienda USL-IRCCS di Reggio Emilia, Viale Risorgimento 80, 42123, Reggio Emilia.
Valentina FragliassoLaboratory of Translational Research, Azienda USL-IRCCS di Reggio Emilia, Viale Risorgimento 80, 42123, Reggio Emilia. Valentina.Fragliasso@ausl.re.it.
Azienda Sanitaria Unità Locale di Reggio Emilia · ITIstituti di Ricovero e Cura a Carattere Scientifico · ITUniversity of Foggia · ITUniversity of Padua · ITAzienda Ospedaliera S.Maria · ITThomas Jefferson University · USUniversity of Perugia · ITWeill Cornell Medicine · US

Funding

Preclinical Models and Therapeutics CoreP01CA229100 · NCI · MAYO CLINIC ARIZONA · PI INGHIRAMI, GIORGIO · 2018 to 2022
$10.2M
NCI NIH HHS P01 CA229100
6 · The paper itself

Abstract

Long non-coding RNA (lncRNA) are emerging as powerful and versatile regulators of transcriptional programs and distinctive biomarkers of progression of T-cell lymphoma. Their role in the aggressive anaplastic lymphoma kinase-negative (ALK-) subtype of anaplastic large cell lymphoma (ALCL) has been elucidated only in part. Starting from our previously identified ALCL-associated lncRNA signature and performing digital gene expression profiling of a retrospective cohort of ALCL, we defined an 11 lncRNA signature able to discriminate among ALCL subtypes. We selected a not previously characterized lncRNA, MTAAT, with preferential expression in ALK- ALCL, for molecular and functional studies. We demonstrated that lncRNA MTAAT contributes to an aberrant mitochondrial turnover restraining mitophagy and promoting cellular proliferation. Functionally, lncRNA MTAAT acts as a repressor of a set of genes related to mitochondrial quality control via chromatin reorganization. Collectively, our work demonstrates the transcriptional role of lncRNA MTAAT in orchestrating a complex transcriptional program sustaining the progression of ALK- ALCL.

Indexed as

Lymphoma, Large-Cell, AnaplasticLymphoma, T-Cell, PeripheralRNA, Long NoncodingAnaplastic Lymphoma KinaseHumansMitophagyReceptor Protein-Tyrosine KinasesRetrospective StudiesAnaplastic Lymphoma KinaseReceptor Protein-Tyrosine KinasesRNA, Long Noncoding

Identifiers

PMID37381763
PMCPMC10690924
OpenAlexW4382501596

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.