Evidence map›Paper›PMID 31417675›Full record

ArticleClinical & translational immunology2019

Expression of IL-34 correlates with macrophage infiltration and prognosis of diffuse large B-cell lymphoma.

Osamu Noyori, Yoshihiro Komohara, Hesham Nasser, Masateru Hiyoshi, Chaoya Ma, Cheng Pan, Joaquim Carreras, Naoya Nakamura, Ai Sato, Kiyoshi Ando and 4 more

Open access · goldAbstract read
In one paragraph

Article in Clinical & translational immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

11 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
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  9. Pharmacogenomics and personalized medicine · 2021
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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

14 authors at 2 institutions in 1 country.

Osamu NoyoriInternational Research Center for Medical Sciences Joint Research Center for Human Retrovirus Infection Kumamoto University Kumamoto Japan.
Yoshihiro KomoharaDepartment of Cell Pathology Graduate School of Medical Sciences Kumamoto University Kumamoto Japan.
Hesham NasserInternational Research Center for Medical Sciences Joint Research Center for Human Retrovirus Infection Kumamoto University Kumamoto Japan.
Masateru HiyoshiInternational Research Center for Medical Sciences Joint Research Center for Human Retrovirus Infection Kumamoto University Kumamoto Japan.
Chaoya MaDepartment of Cell Pathology Graduate School of Medical Sciences Kumamoto University Kumamoto Japan.
Cheng PanDepartment of Cell Pathology Graduate School of Medical Sciences Kumamoto University Kumamoto Japan.
Joaquim CarrerasDepartment of Pathology School of Medicine Tokai University Kanagawa Japan.
Naoya NakamuraDepartment of Pathology School of Medicine Tokai University Kanagawa Japan.
Ai SatoDepartment of Hematology and Oncology School of Medicine Tokai University Kanagawa Japan.
Kiyoshi AndoDepartment of Hematology and Oncology School of Medicine Tokai University Kanagawa Japan.
Yutaka OkunoDepartment of Hematology, Rheumatology, and Infectious Diseases Graduate School of Medical Sciences Kumamoto University Kumamoto Japan.
Kisato NosakaDepartment of Hematology, Rheumatology, and Infectious Diseases Graduate School of Medical Sciences Kumamoto University Kumamoto Japan.
Masao MatsuokaDepartment of Hematology, Rheumatology, and Infectious Diseases Graduate School of Medical Sciences Kumamoto University Kumamoto Japan.
Shinya SuzuInternational Research Center for Medical Sciences Joint Research Center for Human Retrovirus Infection Kumamoto University Kumamoto Japan.ORCID https://orcid.org/0000-0003-2531-4770
Kumamoto University · JPTokai University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesInfiltration of macrophages through the tyrosine kinase receptor CSF1R is a poor prognosis factor in various solid tumors. Indeed, these tumors produce CSF1R ligand, macrophage colony-stimulating factor (M-CSF) or interleukin-34 (IL-34). However, the significance of these cytokines, particularly, the newly discovered IL-34 in haematological malignancies, is not fully understood. We therefore analysed the role of IL-34 in diffuse large B-cell lymphoma (DLBCL), the most common subtype of malignant lymphoma.

methodsWe analysed formalin-fixed paraffin-embedded lymphoma tissues of 135 DLBCL patients for the expression of IL-34 and the number of macrophages, and the survival of these patients. The expression of IL-34 in DLBCL cell lines and the activity of IL-34 to induce the migration of monocytic cells were also characterised.

resultsSeveral lymphoma tissues showed a clear IL-34 signal, and such signal was detectable in 36% of patients. DLBCL cell lines also expressed IL-34. Interestingly, the percentage of IL-34

conclusionOur results raise the possibility that IL-34 in lymphoma tissues of DLBCL patients recruits monocytes, leading to the higher number of macrophages in the tissues and poor prognosis of patients. IL-34 may be an additional therapeutic target of DLBCL.

Indexed as

CSF1RDLBCLIL‐34MacrophagesM‐CSF

Identifiers

PMID31417675
PMCPMC6691654
OpenAlexW2967574116

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.