Evidence map›Paper›PMID 30272010›Full record

ArticleCommunications biology2018

Origin of cancer-associated fibroblasts and tumor-associated macrophages in humans after sex-mismatched bone marrow transplantation.

Masako Kurashige, Masaharu Kohara, Kenji Ohshima, Shinichiro Tahara, Yumiko Hori, Satoshi Nojima, Naoki Wada, Jun-Ichiro Ikeda, Koichi Miyamura, Masafumi Ito and 1 more

Open access · goldAbstract read
In one paragraph

Article in Communications biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.0field-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

24 citing papers in PubMed, 58 citations in OpenAlex.

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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

11 authors at 2 institutions in 1 country.

Masako KurashigeDepartment of Pathology, Graduate School of Medicine, Osaka University, Yamada-Oka, Suita, Osaka, 565-0871, Japan.ORCID http://orcid.org/0000-0001-9212-6644
Masaharu KoharaDepartment of Pathology, Graduate School of Medicine, Osaka University, Yamada-Oka, Suita, Osaka, 565-0871, Japan.
Kenji OhshimaDepartment of Pathology, Graduate School of Medicine, Osaka University, Yamada-Oka, Suita, Osaka, 565-0871, Japan.
Shinichiro TaharaDepartment of Pathology, Graduate School of Medicine, Osaka University, Yamada-Oka, Suita, Osaka, 565-0871, Japan.
Yumiko HoriDepartment of Pathology, Graduate School of Medicine, Osaka University, Yamada-Oka, Suita, Osaka, 565-0871, Japan.
Satoshi NojimaDepartment of Pathology, Graduate School of Medicine, Osaka University, Yamada-Oka, Suita, Osaka, 565-0871, Japan.
Naoki WadaDepartment of Pathology, Graduate School of Medicine, Osaka University, Yamada-Oka, Suita, Osaka, 565-0871, Japan.
Jun-Ichiro IkedaDepartment of Pathology, Graduate School of Medicine, Osaka University, Yamada-Oka, Suita, Osaka, 565-0871, Japan.
Koichi MiyamuraDepartment of Hematology, Japanese Red Cross Nagoya First Hospital, 3-35 Michishita-cho, Nakamura-ku, Nagoya, Japan.
Masafumi ItoDepartment of Pathology, Japanese Red Cross Nagoya First Hospital, 3-35 Michishita-cho, Nakamura-ku, Nagoya, Japan.
Eiichi MoriiDepartment of Pathology, Graduate School of Medicine, Osaka University, Yamada-Oka, Suita, Osaka, 565-0871, Japan. morii@molpath.med.osaka-u.ac.jp.
The University of Osaka · JPJapanese Red Cross Nagoya Daiichi Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer-associated fibroblasts (CAFs) and tumor-associated macrophages (TAMs) in tumor stroma play a key role in disease progression. Recent studies using mice models suggest that CAFs are partly derived from bone marrow and TAMs primarily originate from bone marrow-derived inflammatory monocytes. However, the origin of these cells in humans remains unclear. Hence, we investigated their human origin, using specimens from human secondary tumors that developed after sex-mismatched bone marrow transplantation, by modified immunofluorescent in situ hybridization analysis and triple immunostaining. We observed that most of the α-smooth muscle actin (αSMA)-positive CAFs in the mammary gland, liver, and oral mucosa specimens obtained 3-19 years after bone marrow transplantation are recipient-derived cells. In contrast, the majority of the peritumoral αSMA-negative fibroblast-like cells are actually bone marrow-derived HLA-DR-positive myeloid cells, such as macrophages and dendritic cells. Furthermore, almost all CD163-positive TAMs and macrophages present in the non-tumor areas are derived from bone marrow.

Identifiers

PMID30272010
PMCPMC6123637
OpenAlexW2889549435

What OpenQuestion holds

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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.