Evidence map›Paper›PMID 36926576›Full record

ArticleNanoscale advances2023

The potential role of serum extracellular vesicle derived small RNAs in AML research as non-invasive biomarker.

Lin Li, Veronika Mussack, André Görgens, Elena Pepeldjiyska, Anne Sophie Hartz, Hazal Aslan, Elias Rackl, Andreas Rank, Jörg Schmohl, Samir El Andaloussi and 2 more

Open access · goldAbstract read
In one paragraph

Article in Nanoscale advances, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
2.0field-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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 13 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
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

12 authors at 4 institutions in 2 countries.

Lin LiImmune-Modulation, Medical Department III, University Hospital of Munich Marchioninistraße 15 81377 Munich Germany Lin.Li0814@outlook.com elena.pepeldjiyska@gmail.com as.hartz@t-online.de hazlaslan@gmail.com elias.rackl@hotmail.de Helga.Schmetzer@med.uni-muenchen.de +49 89 4400 76137 +49 89 4400 73137.ORCID https://orcid.org/0000-0003-2557-6404
Veronika MussackDepartment of Animal Physiology and Immunology, TUM School of Life Sciences Weihenstephan, Technical University of Munich Freising Germany veronika.mussack@mytum.de michael.pfaffl@tum.de.
André GörgensDepartment of Laboratory Medicine, Division of Biomolecular and Cellular Medicine, Karolinska Institutet Stockholm Sweden andre.gorgens@ki.se Samir.El-Andaloussi@ki.se.
Elena PepeldjiyskaImmune-Modulation, Medical Department III, University Hospital of Munich Marchioninistraße 15 81377 Munich Germany Lin.Li0814@outlook.com elena.pepeldjiyska@gmail.com as.hartz@t-online.de hazlaslan@gmail.com elias.rackl@hotmail.de Helga.Schmetzer@med.uni-muenchen.de +49 89 4400 76137 +49 89 4400 73137.
Anne Sophie HartzImmune-Modulation, Medical Department III, University Hospital of Munich Marchioninistraße 15 81377 Munich Germany Lin.Li0814@outlook.com elena.pepeldjiyska@gmail.com as.hartz@t-online.de hazlaslan@gmail.com elias.rackl@hotmail.de Helga.Schmetzer@med.uni-muenchen.de +49 89 4400 76137 +49 89 4400 73137.
Hazal AslanImmune-Modulation, Medical Department III, University Hospital of Munich Marchioninistraße 15 81377 Munich Germany Lin.Li0814@outlook.com elena.pepeldjiyska@gmail.com as.hartz@t-online.de hazlaslan@gmail.com elias.rackl@hotmail.de Helga.Schmetzer@med.uni-muenchen.de +49 89 4400 76137 +49 89 4400 73137.
Elias RacklImmune-Modulation, Medical Department III, University Hospital of Munich Marchioninistraße 15 81377 Munich Germany Lin.Li0814@outlook.com elena.pepeldjiyska@gmail.com as.hartz@t-online.de hazlaslan@gmail.com elias.rackl@hotmail.de Helga.Schmetzer@med.uni-muenchen.de +49 89 4400 76137 +49 89 4400 73137.
Andreas RankDepartment of Hematology and Oncology, University Hospital of Augsburg Augsburg Germany andreas.rank@uk-augsburg.de.
Jörg SchmohlDepartment of Hematology and Oncology, Hospital of Stuttgart Stuttgart Germany joerg.schmohl@diak-stuttgart.de.
Samir El AndaloussiDepartment of Laboratory Medicine, Division of Biomolecular and Cellular Medicine, Karolinska Institutet Stockholm Sweden andre.gorgens@ki.se Samir.El-Andaloussi@ki.se.
Michael W PfafflDepartment of Animal Physiology and Immunology, TUM School of Life Sciences Weihenstephan, Technical University of Munich Freising Germany veronika.mussack@mytum.de michael.pfaffl@tum.de.
Helga SchmetzerImmune-Modulation, Medical Department III, University Hospital of Munich Marchioninistraße 15 81377 Munich Germany Lin.Li0814@outlook.com elena.pepeldjiyska@gmail.com as.hartz@t-online.de hazlaslan@gmail.com elias.rackl@hotmail.de Helga.Schmetzer@med.uni-muenchen.de +49 89 4400 76137 +49 89 4400 73137.
Karolinska Institutet · SETechnical University of Munich · DEKlinikum Stuttgart · DEUniversity Hospital Augsburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundExtracellular vesicles (EV) are cell-derived vesicles released by all cells in health and disease. Accordingly, EVs are also released by cells in acute myeloid leukemia (AML), a hematologic malignancy characterized by uncontrolled growth of immature myeloid cells, and these EVs likely carry markers and molecular cargo reflecting the malignant transformation occurring in diseased cells. Monitoring antileukemic or proleukemic processes during disease development and treatment is essential. Therefore, EVs and EV-derived microRNA (miRNA) from AML samples were explored as biomarkers to distinguish disease-related patterns METHODOLOGY: EVs were purified from serum of healthy (H) volunteers and AML patients by immunoaffinity. EV surface protein profiles were analyzed by multiplex bead-based flow cytometry (MBFCM) and total RNA was isolated from EVs prior to miRNA profiling

resultsMBFCM revealed different surface protein patterns in H

conclusionsIn this study, we provide a proof-of-concept for the discriminative potential of EV derived miRNA profiles as biomarkers in H

Identifiers

PMID36926576
PMCPMC10012871
OpenAlexW4321379898

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.