Evidence map›Paper›PMID 36550553›Full record

ArticleMolecular cancer2022

Extracellular vesicle microRNAs contribute to Notch signaling pathway in T-cell acute lymphoblastic leukemia.

Tommaso Colangelo, Patrizio Panelli, Francesco Mazzarelli, Francesco Tamiro, Valentina Melocchi, Elisabetta De Santis, Roberto Cuttano, Orazio Palumbo, Giovanni Rossi, Fabrizio Bianchi and 1 more

Open access · goldAbstract readLetter
In one paragraph

Article in Molecular cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

15 citing papers in PubMed, 15 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

11 authors at 2 institutions in 1 country.

Tommaso ColangeloUnit of Cancer Biomarker, Fondazione IRCCS Casa Sollievo Della Sofferenza, Viale Padre Pio 7, 71013, San Giovanni Rotondo, FG, Italy.
Patrizio PanelliUnit of Hematopathology, Fondazione IRCCS Casa Sollievo Della Sofferenza, Viale Padre Pio 7, 71013, San Giovanni Rotondo, FG, Italy.
Francesco MazzarelliUnit of Cancer Biomarker, Fondazione IRCCS Casa Sollievo Della Sofferenza, Viale Padre Pio 7, 71013, San Giovanni Rotondo, FG, Italy.
Francesco TamiroUnit of Hematopathology, Fondazione IRCCS Casa Sollievo Della Sofferenza, Viale Padre Pio 7, 71013, San Giovanni Rotondo, FG, Italy.
Valentina MelocchiUnit of Cancer Biomarker, Fondazione IRCCS Casa Sollievo Della Sofferenza, Viale Padre Pio 7, 71013, San Giovanni Rotondo, FG, Italy.
Elisabetta De SantisUnit of Hematopathology, Fondazione IRCCS Casa Sollievo Della Sofferenza, Viale Padre Pio 7, 71013, San Giovanni Rotondo, FG, Italy.
Roberto CuttanoUnit of Cancer Biomarker, Fondazione IRCCS Casa Sollievo Della Sofferenza, Viale Padre Pio 7, 71013, San Giovanni Rotondo, FG, Italy.
Orazio PalumboDivision of Medical Genetics, Fondazione IRCCS Casa Sollievo Della Sofferenza, 71013, San Giovanni Rotondo, FG, Italy.
Giovanni RossiDepartment of Hematology and Stem Cell Transplant Unit, Fondazione IRCCS Casa Sollievo Della Sofferenza, 71013, San Giovanni Rotondo, FG, Italy.
Fabrizio Bianchi *Unit of Cancer Biomarker, Fondazione IRCCS Casa Sollievo Della Sofferenza, Viale Padre Pio 7, 71013, San Giovanni Rotondo, FG, Italy. f.bianchi@operapadrepio.it.
Vincenzo Giambra *Unit of Hematopathology, Fondazione IRCCS Casa Sollievo Della Sofferenza, Viale Padre Pio 7, 71013, San Giovanni Rotondo, FG, Italy. v.giambra@operapadrepio.it.
Casa Sollievo della Sofferenza · ITIstituti di Ricovero e Cura a Carattere Scientifico · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

T-cell acute lymphoblastic leukemia (T-ALL) is an aggressive T-cell malignancy characterized by genotypically-defined and phenotypically divergent cell populations, governed by adaptive landscapes. Clonal expansions are associated to genetic and epigenetic events, and modulation of external stimuli that affect the hierarchical structure of subclones and support the dynamics of leukemic subsets. Recently, small extracellular vesicles (sEV) such as exosomes were also shown to play a role in leukemia. Here, by coupling miRNome, bulk and single cell transcriptome profiling, we found that T-ALL-secreted sEV contain NOTCH1-dependent microRNAs (EV-miRs), which control oncogenic pathways acting as autocrine stimuli and ultimately promoting the expansion/survival of highly proliferative cell subsets of human T-cell leukemias. Of interest, we found that NOTCH1-dependent EV-miRs mostly comprised members of miR-17-92a cluster and paralogues, which rescued in vitro the proliferation of T-ALL cells blocked by γ-secretase inhibitors (GSI) an regulated a network of genes characterizing patients with relapsed/refractory early T-cell progenitor (ETP) ALLs. All these findings suggest that NOTCH1 dependent EV-miRs may sustain the growth/survival of immunophenotypically defined cell populations, altering the cell heterogeneity and the dynamics of T-cell leukemias in response to conventional therapies.

Indexed as

Extracellular VesiclesMicroRNAsPrecursor T-Cell Lymphoblastic Leukemia-LymphomaAmyloid Precursor Protein SecretasesHumansReceptor, Notch1Signal TransductionAmyloid Precursor Protein SecretasesMicroRNAsReceptor, Notch1ExosomesExtracellular vesiclesGene expressionmicroRNAsT-cell acute lymphoblastic leukemia

Identifiers

PMID36550553
PMCPMC9773489
OpenAlexW4312190599

What OpenQuestion holds

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Registered trials

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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.