Evidence map›Paper›PMID 30701702›Full record

ArticleCancer medicine2019

Disruption of erythroid nuclear opening and histone release in myelodysplastic syndromes.

Baobing Zhao, Hui Liu, Yang Mei, Yijie Liu, Xu Han, Jing Yang, Amittha Wickrema, Peng Ji

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

19 citing papers in PubMed, 28 citations in OpenAlex.

  1. Blood Pharming of Red Cells.Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie · 2026
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  13. Proteomic/transcriptomic analysis of erythropoiesis.Current opinion in hematology · 2021
    Review
  14. Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. 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

8 authors at 2 institutions in 2 countries.

Baobing ZhaoDepartment of Pathology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois.ORCID 0000-0001-8522-4764
Hui LiuSection of Hematology/Oncology, Department of Medicine, The University of Chicago, Chicago, Illinois.
Yang MeiDepartment of Pathology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois.
Yijie LiuDepartment of Pathology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois.
Xu HanDepartment of Pathology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois.
Jing YangDepartment of Pathology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois.
Amittha WickremaSection of Hematology/Oncology, Department of Medicine, The University of Chicago, Chicago, Illinois.
Peng JiDepartment of Pathology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois.
Northwestern University · USUniversity of Chicago · US

Funding

The roles of pleckstrin-2 as a functional node in erythropoiesisR01DK102718 · NIDDK · NORTHWESTERN UNIVERSITY AT CHICAGO · PI JI, PENG · 2015 to 2019
$1.7M
NIDDK NIH HHS R01 DK102718
6 · The paper itself

Abstract

Mammalian terminal erythropoiesis involves several characteristic phenomena including chromatin condensation and enucleation. One of the newly identified features of terminal erythropoiesis in mouse is a dynamic nuclear opening and histone release process, which is required for chromatin condensation. However, it is unclear whether the same feature is present in human. Here, we use an in vitro human CD34-positive hematopoietic stem and progenitor cell culture system and reveal that nuclear openings and histone release are also identified during human terminal erythropoiesis. In contrast to mouse in which each erythroblast contains a single opening, multiple nuclear openings are present in human erythroblast, particularly during the late-stage differentiation. The nuclear opening and histone release process is mediated by caspase-3. Inhibition of caspase-3 blocks nuclear opening, histone release, chromatin condensation, and terminal differentiation. We confirm the finding of histone cytosolic release in paraffin-embedded human bone marrow in vivo. Importantly, we find that patients with myelodysplastic syndrome (MDS) exhibit significant defects in histone release in the dysplastic erythroblasts. Our results reveal developmentally conserved nuclear envelop and histone dynamic changes in human terminal erythropoiesis and indicate that disruption of the histone release process plays a critical role in the pathogenesis of dyserythropoiesis in MDS.

Indexed as

Caspase 3Cell DifferentiationCell NucleusChromatinErythroblastsErythropoiesisHistonesHumansImmunohistochemistryMyelodysplastic SyndromesCASP3 protein, humanCaspase 3ChromatinHistoneschromatin condensationenucleationerythropoiesismyelodysplastic syndromes

Identifiers

PMID30701702
PMCPMC6434191
OpenAlexW2914023395

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.