Evidence map›Paper›PMID 32948017›Full record

ArticleInternational journal of molecular sciences2020

A Screening of Antineoplastic Drugs for Acute Myeloid Leukemia Reveals Contrasting Immunogenic Effects of Etoposide and Fludarabine.

Darina Ocadlikova, Clara Iannarone, Anna Rita Redavid, Michele Cavo, Antonio Curti

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
0.5field-weighted citation impact, top 32% 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

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Immunogenic Cell Death in Hematological Malignancy Therapy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2023
    Review
  5. 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

5 authors at 2 institutions in 1 country.

Darina OcadlikovaDipartimento di Medicina Specialistica, Diagnostica e Sperimentale, Istituto di Ematologia "Seràgnoli", Università degli Studi, 40138 Bologna, Italy.
Clara IannaroneDipartimento di Medicina Specialistica, Diagnostica e Sperimentale, Istituto di Ematologia "Seràgnoli", Università degli Studi, 40138 Bologna, Italy.ORCID 0000-0001-6618-6694
Anna Rita RedavidDipartimento di Medicina Specialistica, Diagnostica e Sperimentale, Istituto di Ematologia "Seràgnoli", Università degli Studi, 40138 Bologna, Italy.ORCID 0000-0002-1332-2792
Michele CavoDipartimento di Medicina Specialistica, Diagnostica e Sperimentale, Istituto di Ematologia "Seràgnoli", Università degli Studi, 40138 Bologna, Italy.
Antonio CurtiAzienda Ospedaliero-Universitaria di Bologna, via Albertoni 15, 40138 Bologna, Italy.
Istituto di Ematologia di Bologna · ITAzienda USL di Bologna · IT

Funding

Associazione Italiana Contro le Leucemie-Linfomi e Mieloma Bologna sectionAssociazione Italiana per la Ricerca sul Cancro 2017 IG20654Foundation Corrado and Bruno Maria Zaini-Bologna Foundation Corrado and Bruno Maria Zaini-Bologna
6 · The paper itself

Abstract

backgroundRecent evidence demonstrated that the treatment of acute myeloid leukemia (AML) cells with daunorubicin (DNR) but not cytarabine (Ara-C) results in immunogenic cell death (ICD). In the clinical setting, chemotherapy including anthracyclines and Ara-C remains a gold standard for AML treatment. In the last decade, etoposide (Eto) and fludarabine (Flu) have been added to the standard treatment for AML to potentiate its therapeutic effect and have been tested in many trials. Very little data are available about the ability of these drugs to induce ICD.

methodsAML cells were treated with all four drugs. Calreticulin and heat shock protein 70/90 translocation, non-histone chromatin-binding protein high mobility group box 1 and adenosine triphosphate release were evaluated. The treated cells were pulsed into dendritic cells (DCs) and used for in vitro immunological tests.

resultsFlu and Ara-C had no capacity to induce ICD-related events. Interestingly, Eto was comparable to DNR in inducing all ICD events, resulting in DC maturation. Moreover, Flu was significantly more potent in inducing suppressive T regulatory cells compared to other drugs.

conclusionsOur results indicate a novel and until now poorly investigated feature of antineoplastic drugs commonly used for AML treatment, based on their different immunogenic potential.

Indexed as

Adenosine TriphosphateAlarminsAntineoplastic AgentsCalreticulinCell Line, TumorCytarabineDaunorubicinDendritic CellsEtoposideExtracellular SpaceGene Expression Regulation, NeoplasticHeat-Shock ProteinsHumansImmunogenic Cell DeathLeukemia, Myeloid, AcuteLymphocyte ActivationAdenosine TriphosphateAlarminsAntineoplastic AgentsCalreticulinCALR protein, humanCytarabineDaunorubicinEtoposidefludarabineHeat-Shock ProteinsNeoplasm ProteinsVidarabineacute myeloid leukemiachemotherapyetoposidefludarabineimmunogenic cell death

Identifiers

PMID32948017
PMCPMC7556041
OpenAlexW3085300433

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.