Evidence map›Paper›PMID 38499475›Full record

ArticleJournal of extracellular vesicles2024

Y-box binding protein 1 in small extracellular vesicles reduces mesenchymal stem cell differentiation to osteoblasts-implications for acute myeloid leukaemia.

Venkatesh Kumar Chetty, Jamal Ghanam, Kristína Lichá, Alexandra Brenzel, Dirk Reinhardt, Basant Kumar Thakur

Open access · goldAbstract read
In one paragraph

Article in Journal of extracellular vesicles, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

9 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. miR-379-5p Inhibited the Proliferation of Acute Myeloid Leukemia Cells Through Negative Regulation ofTurkish journal of haematology : official journal of Turkish Society of Haematology · 2025
    Article
  5. Review
  6. Review
  7. YBX1 alleviates ferroptosis in osteoporosis via the ATF4/FSP1 axis in an mJournal of orthopaedic surgery and research · 2025
    Article
  8. Review
  9. 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

6 authors at 1 institution in 2 countries.

Venkatesh Kumar ChettyDepartment of Pediatrics III, University Hospital Essen, Essen, Germany.ORCID https://orcid.org/0000-0002-2572-2494
Jamal GhanamDepartment of Pediatrics III, University Hospital Essen, Essen, Germany.ORCID https://orcid.org/0000-0003-0077-6098
Kristína LicháDepartment of Pediatrics III, University Hospital Essen, Essen, Germany.
Alexandra BrenzelImaging Center Essen (IMCES), University Hospital Essen, Essen, Germany.
Dirk ReinhardtDepartment of Pediatrics III, University Hospital Essen, Essen, Germany.
Basant Kumar ThakurDepartment of Pediatrics III, University Hospital Essen, Essen, Germany.ORCID https://orcid.org/0000-0001-7013-7895
Essen University Hospital · DE

Funding

Deutsche Forschungsgemeinschaft TH 2012/1-1Deutsche Kinderkrebsstiftung DKS 2018.17José Carreras Leukämie-Stiftung DJCLS 14 R/2023Stiftung Universitätsmedizin Essen
6 · The paper itself

Abstract

Small extracellular vesicles (sEVs) released by acute myeloid leukaemia (AML) cells have been reported to influence the trilineage differentiation of bone marrow-derived mesenchymal stem cells (BM-MSCs). However, it remains elusive which biological cargo from AML-sEVs is responsible for this effect. In this study, sEVs were isolated from cell-conditioned media and blood plasma using size-exclusion chromatography and ultrafiltration and characterized according to MISEV2018 guidelines. Our results demonstrated that AML-sEVs increased the proliferation of BM-MSCs. Conversely, key proteins that are important for normal haematopoiesis were downregulated in BM-MSCs. Additionally, we revealed that AML-sEVs significantly reduced the differentiation of BM-MSCs to osteoblasts without affecting adipogenic or chondrogenic differentiation. Next, LC-MS/MS proteomics elucidated that various proteins, including Y-box-binding protein 1 (YBX1), were upregulated in both AML-sEVs and BM-MSCs treated with AML-sEVs. Clinically relevant, we found that YBX1 is considerably upregulated in most paediatric AML patient-derived sEVs compared to healthy controls. Interestingly, sEVs isolated after the downregulation of YBX1 in AML cells remarkably rescued the osteoblastic differentiation of BM-MSCs. Altogether, our data demonstrate for the first time that YBX1 containing AML-sEVs is one of the key players that disrupt the normal function of bone marrow microenvironment by reducing the osteogenic differentiation of BM-MSCs.

Indexed as

Extracellular VesiclesLeukemia, Myeloid, AcuteMesenchymal Stem CellsChildChromatography, LiquidHumansOsteoblastsOsteogenesisTandem Mass SpectrometryTumor MicroenvironmentY-Box-Binding Protein 1Y-Box-Binding Protein 1YBX1 protein, humanacute myeloid leukaemiabone marrow microenvironmentmesenchymal stem cellsosteoblastssmall extracellular vesiclesY-box binding protein 1

Identifiers

PMID38499475
PMCPMC10948369
OpenAlexW4392967280

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.