Evidence map›Paper›PMID 26802051›Full record

ArticleHaematologica2016

Extracellular vesicle miR-7977 is involved in hematopoietic dysfunction of mesenchymal stromal cells via poly(rC) binding protein 1 reduction in myeloid neoplasms.

Hiroto Horiguchi, Masayoshi Kobune, Shohei Kikuchi, Masahiro Yoshida, Masaki Murata, Kazuyuki Murase, Satoshi Iyama, Kohichi Takada, Tsutomu Sato, Kaoru Ono and 7 more

Open access · goldAbstract read
In one paragraph

Article in Haematologica, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
5.5field-weighted citation impact, top 4% 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

47 citing papers in PubMed, 77 citations in OpenAlex.

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  16. Iron as spirit of life to share under monopoly.Journal of clinical biochemistry and nutrition · 2022
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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

17 authors at 1 institution in 1 country.

Hiroto HoriguchiDepartment of Medical Oncology and Hematology, Sapporo Medical University School of Medicine, Japan.
Masayoshi KobuneDepartment of Medical Oncology and Hematology, Sapporo Medical University School of Medicine, Japan mkobune@sapmed.ac.jp.
Shohei KikuchiDepartment of Medical Oncology and Hematology, Sapporo Medical University School of Medicine, Japan.
Masahiro YoshidaDepartment of Medical Oncology and Hematology, Sapporo Medical University School of Medicine, Japan.
Masaki MurataDepartment of Pathology, Sapporo Medical University School of Medicine, Japan.
Kazuyuki MuraseDepartment of Medical Oncology and Hematology, Sapporo Medical University School of Medicine, Japan.
Satoshi IyamaDepartment of Medical Oncology and Hematology, Sapporo Medical University School of Medicine, Japan.
Kohichi TakadaDepartment of Medical Oncology and Hematology, Sapporo Medical University School of Medicine, Japan.
Tsutomu SatoDepartment of Medical Oncology and Hematology, Sapporo Medical University School of Medicine, Japan.
Kaoru OnoDepartment of Medical Oncology and Hematology, Sapporo Medical University School of Medicine, Japan.
Akari HashimotoDepartment of Medical Oncology and Hematology, Sapporo Medical University School of Medicine, Japan.
Ayumi TatekoshiDepartment of Medical Oncology and Hematology, Sapporo Medical University School of Medicine, Japan.
Yusuke KamiharaDepartment of Medical Oncology and Hematology, Sapporo Medical University School of Medicine, Japan.
Yutaka KawanoDepartment of Medical Oncology and Hematology, Sapporo Medical University School of Medicine, Japan.
Koji MiyanishiDepartment of Medical Oncology and Hematology, Sapporo Medical University School of Medicine, Japan.
Norimasa SawadaDepartment of Pathology, Sapporo Medical University School of Medicine, Japan.
Junji KatoDepartment of Medical Oncology and Hematology, Sapporo Medical University School of Medicine, Japan.
Sapporo Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The failure of normal hematopoiesis is observed in myeloid neoplasms. However, the precise mechanisms governing the replacement of normal hematopoietic stem cells in their niche by myeloid neoplasm stem cells have not yet been clarified. Primary acute myeloid leukemia and myelodysplastic syndrome cells induced aberrant expression of multiple hematopoietic factors including Jagged-1, stem cell factor and angiopoietin-1 in mesenchymal stem cells even in non-contact conditions, and this abnormality was reverted by extracellular vesicle inhibition. Importantly, the transfer of myeloid neoplasm-derived extracellular vesicles reduced the hematopoietic supportive capacity of mesenchymal stem cells. Analysis of extracellular vesicle microRNA indicated that several species, including miR-7977 from acute myeloid leukemia cells, were higher than those from normal CD34(+)cells. Remarkably, the copy number of miR-7977 in bone marrow interstitial fluid was elevated not only in acute myeloid leukemia, but also in myelodysplastic syndrome, as compared with lymphoma without bone marrow localization. The transfection of the miR-7977 mimic reduced the expression of the posttranscriptional regulator, poly(rC) binding protein 1, in mesenchymal stem cells. Moreover, the miR-7977 mimic induced aberrant reduction of hematopoietic growth factors in mesenchymal stem cells, resulting in decreased hematopoietic-supporting capacity of bone marrow CD34(+)cells. Furthermore, the reduction of hematopoietic growth factors including Jagged-1, stem cell factor and angiopoietin-1 were reverted by target protection of poly(rC) binding protein 1, suggesting that poly(rC) binding protein 1 could be involved in the stabilization of several growth factors. Thus, miR-7977 in extracellular vesicles may be a critical factor that induces failure of normal hematopoiesis via poly(rC) binding protein 1 suppression.

Indexed as

Gene Expression Regulation, NeoplasticAngiopoietin-1Bone Marrow CellsCoculture TechniquesDNA-Binding ProteinsExtracellular VesiclesGene Expression ProfilingHematopoiesisHeterogeneous-Nuclear RibonucleoproteinsHumansJagged-1 ProteinLeukemia, Myeloid, AcuteLymphomaMesenchymal Stem CellsMicroRNAsMolecular MimicryAngiopoietin-1ANGPT1 protein, humanDNA-Binding ProteinsHeterogeneous-Nuclear RibonucleoproteinsJagged-1 ProteinMicroRNAsMIRN7977 microRNA, humanOligoribonucleotidesPCBP1 protein, humanRNA-Binding ProteinsStem Cell Factor

Identifiers

PMID26802051
PMCPMC5004399
OpenAlexW2262398248

What OpenQuestion holds

Textmetadata
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.