Evidence map›Paper›PMID 34575936›Full record

ArticleInternational journal of molecular sciences2021

Extracellular Vesicle MicroRNA That Are Involved in β-Thalassemia Complications.

Carina Levin, Ariel Koren, Annie Rebibo-Sabbah, Maya Levin, Na'ama Koifman, Benjamin Brenner, Anat Aharon

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Potential Use of MicroRNA Technology in Thalassemia Therapy.Journal of clinical medicine research · 2024
    Review
  6. Article
  7. Review
  8. Review
  9. Post-transcriptional regulation of erythropoiesis.Blood science (Baltimore, Md.) · 2023
    Review
  10. Review
  11. Article
  12. The Role of Exosomes in Health and Disease.International journal of molecular sciences · 2022
    Article
  13. 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

7 authors at 3 institutions in 1 country.

Carina LevinPediatric Hematology Unit, Emek Medical Center, Afula 1834111, Israel.ORCID 0000-0002-7774-3529
Ariel KorenPediatric Hematology Unit, Emek Medical Center, Afula 1834111, Israel.
Annie Rebibo-SabbahDepartment of Hematology and Bone Marrow Transplantation, Rambam Health Care Campus, Haifa 3109601, Israel.
Maya LevinThe Hematology Research Laboratory, Tel Aviv Sourasky Medical Center, Tel Aviv 6423906, Israel.
Na'ama KoifmanDepartment of Chemical Engineering and the Russell Berrie Nanotechnology Institute, Technion-Israel Institute of Technology, Haifa 3200003, Israel.ORCID 0000-0002-2017-3027
Benjamin BrennerBruce Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa 3109601, Israel.
Anat AharonBruce Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa 3109601, Israel.
Technion – Israel Institute of Technology · ILRambam Health Care Campus · ILTel Aviv Sourasky Medical Center · IL

Funding

Israel Science Foundation 1957/17
6 · The paper itself

Abstract

Beta thalassemia major (βT) is a hereditary anemia characterized by transfusion-dependency, lifelong requirement of chelation, and organ dysfunction. MicroRNA (miRNA) can be packed into extracellular vesicles (EVs) that carry them to target cells. We explored EV-miRNA in βT and their pathophysiologic role. Circulating EVs were isolated from 35 βT-patients and 15 controls. EV miRNA was evaluated by nano-string technology and real-time quantitative polymerase chain reaction (RT-qPCR). We explored effects of EVs on cell culture proliferation, apoptosis, and signal transduction. Higher amounts of small EV (exosomes) were found in patients than in controls. The expression of 21 miRNA was > two-fold higher, and of 17 miRNA < three-fold lower in βT-EVs than control-EVs. RT-qPCR confirmed differential expression of six miRNAs in βT, particularly miR-144-3p, a regulator of erythropoiesis. Exposure of endothelial, liver Huh7, and pancreatic 1.1B4 cells to βT-EVs significantly reduced cell viability and increased cell apoptosis. βT-EV-induced endothelial cell apoptosis involved the MAPK/JNK signal-transduction pathway. In contrast, splenectomized βT-EVs induced proliferation of bone marrow mesenchymal stem cells (BM-MSC). In summary, the miR-144-3p was strongly increased; βT-EVs induced apoptosis and decreased endothelial, pancreatic, and liver cell survival while supporting BM-MSC proliferation. These mechanisms may contribute to βT organ dysfunction and complications.

Indexed as

AdolescentAdultApoptosisbeta-ThalassemiaBiological TransportCase-Control StudiesCell LineCell SurvivalExosomesExtracellular VesiclesFemaleGene Expression ProfilingHumansMaleMicroRNAsSignal TransductionMicroRNAsextracellular vesicles (EVs)microRNA (miRNA)signal-transductionβ-thalassemia major

Identifiers

PMID34575936
PMCPMC8465435
OpenAlexW3198314615

What OpenQuestion holds

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LicenceCC BY
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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.