Evidence map›Paper›PMID 29945938›Full record

ArticleBlood advances2018

Distinct roles of mesenchymal stem and progenitor cells during the development of acute myeloid leukemia in mice.

Pingnan Xiao, Lakshmi Sandhow, Yaser Heshmati, Makoto Kondo, Thibault Bouderlique, Monika Dolinska, Anne-Sofie Johansson, Mikael Sigvardsson, Marja Ekblom, Julian Walfridsson and 1 more

Open access · goldAbstract read
In one paragraph

Article in Blood advances, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

27 citing papers in PubMed, 37 citations in OpenAlex.

  1. Neuro-associated SEMA3CClinical and translational medicine · 2026
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  20. Regulation of Malignant Myeloid Leukemia by Mesenchymal Stem Cells.Frontiers in cell and developmental biology · 2022
    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

11 authors at 3 institutions in 1 country.

Pingnan XiaoCenter for Hematology and Regenerative Medicine, Department of Medicine, Karolinska Institute, Karolinska University Hospital, Stockholm, Sweden.ORCID 0000-0003-1308-4357
Lakshmi SandhowCenter for Hematology and Regenerative Medicine, Department of Medicine, Karolinska Institute, Karolinska University Hospital, Stockholm, Sweden.
Yaser HeshmatiCenter for Hematology and Regenerative Medicine, Department of Medicine, Karolinska Institute, Karolinska University Hospital, Stockholm, Sweden.
Makoto KondoCenter for Hematology and Regenerative Medicine, Department of Medicine, Karolinska Institute, Karolinska University Hospital, Stockholm, Sweden.
Thibault BouderliqueCenter for Hematology and Regenerative Medicine, Department of Medicine, Karolinska Institute, Karolinska University Hospital, Stockholm, Sweden.
Monika DolinskaCenter for Hematology and Regenerative Medicine, Department of Medicine, Karolinska Institute, Karolinska University Hospital, Stockholm, Sweden.
Anne-Sofie JohanssonCenter for Hematology and Regenerative Medicine, Department of Medicine, Karolinska Institute, Karolinska University Hospital, Stockholm, Sweden.
Mikael SigvardssonDepartment of Clinical and Experimental Medicine, Linköping University, Linköping, Sweden; and.ORCID 0000-0001-8527-7276
Marja EkblomDivision of Molecular Hematology, Department of Laboratory Medicine, Lund University, Lund, Sweden.
Julian WalfridssonCenter for Hematology and Regenerative Medicine, Department of Medicine, Karolinska Institute, Karolinska University Hospital, Stockholm, Sweden.ORCID 0000-0002-5038-5063
Hong QianCenter for Hematology and Regenerative Medicine, Department of Medicine, Karolinska Institute, Karolinska University Hospital, Stockholm, Sweden.ORCID 0000-0002-2512-9199
Karolinska University Hospital · SELinköping University · SELund University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite increasing evidence for the involvement of bone marrow (BM) hematopoietic stem cell niche in leukemogenesis, how BM mesenchymal stem and progenitor cells (MSPCs) contribute to leukemia niche formation and progression remains unclear. Using an MLL-AF9 acute myeloid leukemia (AML) mouse model, we demonstrate dynamic alterations of BM cellular niche components, including MSPCs and endothelial cells during AML development and its association with AML engraftment. Primary patient AML cells also induced similar niche alterations in xenografted mice. AML cell infiltration in BM causes an expansion of early B-cell factor 2

Indexed as

AnimalsBasic Helix-Loop-Helix ProteinsBone MarrowCarcinogenesisLeukemia, Myeloid, AcuteMesenchymal Stem CellsMiceMyeloid-Lymphoid Leukemia ProteinOncogene Proteins, FusionStem Cell NicheTransplantation, HeterologousTumor BurdenTumor MicroenvironmentBasic Helix-Loop-Helix ProteinsEbf2 protein, mouseMLL-AF9 fusion protein, humanMyeloid-Lymphoid Leukemia ProteinOncogene Proteins, Fusion

Identifiers

PMID29945938
PMCPMC6020803
OpenAlexW2811355377

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.