Evidence map›Paper›PMID 30782613›Full record

ArticleBlood advances2019

A role for IL-34 in osteolytic disease of multiple myeloma.

Muhammad Baghdadi, Kozo Ishikawa, Sayaka Nakanishi, Tomoki Murata, Yui Umeyama, Takuto Kobayashi, Yosuke Kameda, Hiraku Endo, Haruka Wada, Bjarne Bogen and 10 more

Open access · goldAbstract read
In one paragraph

Article in Blood advances, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.8field-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

22 citing papers in PubMed, 29 citations in OpenAlex.

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  20. The M-CSF receptor in osteoclasts and beyond.Experimental & molecular medicine · 2020
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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

20 authors at 4 institutions in 2 countries.

Muhammad BaghdadiDivision of Immunobiology, Institute for Genetic Medicine, Hokkaido University, Sapporo, Japan.ORCID 0000-0002-2347-8889
Kozo IshikawaDivision of Immunobiology, Institute for Genetic Medicine, Hokkaido University, Sapporo, Japan.
Sayaka NakanishiDivision of Immunobiology, Institute for Genetic Medicine, Hokkaido University, Sapporo, Japan.
Tomoki MurataDivision of Immunobiology, Institute for Genetic Medicine, Hokkaido University, Sapporo, Japan.
Yui UmeyamaDivision of Immunobiology, Institute for Genetic Medicine, Hokkaido University, Sapporo, Japan.
Takuto KobayashiDivision of Immunobiology, Institute for Genetic Medicine, Hokkaido University, Sapporo, Japan.
Yosuke KamedaDivision of Immunobiology, Institute for Genetic Medicine, Hokkaido University, Sapporo, Japan.
Hiraku EndoDivision of Immunobiology, Institute for Genetic Medicine, Hokkaido University, Sapporo, Japan.
Haruka WadaDivision of Immunobiology, Institute for Genetic Medicine, Hokkaido University, Sapporo, Japan.
Bjarne BogenK. G. Jebsen Centre for Influenza Vaccine Research, University of Oslo, Oslo, Norway.
Satoshi YamamotoDepartment of Hematology, Sapporo City General Hospital, Sapporo, Japan.
Keisuke YamaguchiDepartment of Hematology, Sapporo City General Hospital, Sapporo, Japan.
Ikumi KasaharaDepartment of Hematology, Sapporo City General Hospital, Sapporo, Japan.
Hiroshi IwasakiDepartment of Hematology, Sapporo Kosei General Hospital, Sapporo, Japan; and.
Mutsumi TakahataDepartment of Hematology, Sapporo Kosei General Hospital, Sapporo, Japan; and.
Makoto IbataDepartment of Hematology, Sapporo Kosei General Hospital, Sapporo, Japan; and.
Shuichiro TakahashiDepartment of Hematology, Faculty of Medicine, Hokkaido University, Sapporo, Japan.
Hideki GotoDepartment of Hematology, Faculty of Medicine, Hokkaido University, Sapporo, Japan.
Takanori TeshimaDepartment of Hematology, Faculty of Medicine, Hokkaido University, Sapporo, Japan.
Ken-Ichiro SeinoDivision of Immunobiology, Institute for Genetic Medicine, Hokkaido University, Sapporo, Japan.
Hokkaido University · JPSapporo City General Hospital · JPSapporo Kosei General Hospital · JPUniversity of Oslo · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple myeloma (MM) is a hematological malignancy that grows in multiple sites of the axial skeleton and causes debilitating osteolytic disease. Interleukin-34 (IL-34) is a newly discovered cytokine that acts as a ligand of colony-stimulating factor-1 (CSF-1) receptor and can replace CSF-1 for osteoclast differentiation. In this study, we identify IL-34 as an osteoclastogenic cytokine that accelerates osteolytic disease in MM. IL-34 was found to be expressed in the murine MM cell line MOPC315.BM, and the expression of IL-34 was enhanced by stimulation with proinflammatory cytokines or by bone marrow (BM) stromal cells. MM-cell-derived IL-34 promoted osteoclast formation from mouse BM cells in vitro. Targeting

Indexed as

AnimalsCell LineFemaleGene Expression Regulation, NeoplasticHumansInterleukinsMiceMice, Inbred BALB CMultiple MyelomaOsteolysisRNA InterferenceRNA, Small InterferingTumor Cells, CulturedIL34 protein, humaninterleukin-34, mouseInterleukinsRNA, Small Interfering

Identifiers

PMID30782613
PMCPMC6391661
OpenAlexW2917441255

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.