Evidence map›Paper›PMID 29493401›Full record

ArticleCell cycle (Georgetown, Tex.)2018

Bone marrow-derived mesenchymal stem cells promote cell proliferation of multiple myeloma through inhibiting T cell immune responses via PD-1/PD-L1 pathway.

Dandan Chen, Ping Tang, Linxiang Liu, Fang Wang, Haizhou Xing, Ling Sun, Zhongxing Jiang

Open access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
4.7field-weighted citation impact, top 5% 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

28 citing papers in PubMed, 49 citations in OpenAlex.

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  12. Bone marrow-derived mesenchymal stem cells inhibit CD8Clinical and experimental immunology · 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

7 authors at 1 institution in 1 country.

Dandan Chena Department of Hematology , The first affiliated hospital of Zhengzhou University , Zhengzhou , 450052 , China.
Ping Tanga Department of Hematology , The first affiliated hospital of Zhengzhou University , Zhengzhou , 450052 , China.
Linxiang Liua Department of Hematology , The first affiliated hospital of Zhengzhou University , Zhengzhou , 450052 , China.
Fang Wanga Department of Hematology , The first affiliated hospital of Zhengzhou University , Zhengzhou , 450052 , China.
Haizhou Xinga Department of Hematology , The first affiliated hospital of Zhengzhou University , Zhengzhou , 450052 , China.
Ling Suna Department of Hematology , The first affiliated hospital of Zhengzhou University , Zhengzhou , 450052 , China.
Zhongxing Jianga Department of Hematology , The first affiliated hospital of Zhengzhou University , Zhengzhou , 450052 , China.
First Affiliated Hospital of Zhengzhou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThis study aims to explore the effect of bone marrow mesenchymal stem cells (BMSCs) on multiple myeloma (MM) development and the underlying mechanism. MATERIALS AND

methodsBMSCs from C57BL/6 J mice were isolated and the third passage was used for subsequent experiments. Additionally, a series of in vitro transwell coculture assays were performed to explore the effects of BMSCs on the proliferation of MM cells 5TGM1 and CD4

resultsData revealed that BMSCs significantly promoted 5TGM1 proliferation in a dose-dependent manner. Furthermore, BMSCs administration exerted stimulatory effects on MM development in terms of shortening the mouse survival rate, promoting tumor growth, and enhancing inflammatory infiltration in the MM model mice. Moreover, BMSCs decreased the percentage of Th1 and Th17 cells, whereas increased that of Th2 and Treg cells. Their corresponding cytokines of these T cell subsets showed similar alteration in the presence of BMSCs. Additionally, BMSCs significantly suppressed CD4

conclusionIn summary, our findings demonstrated that BMSCs promoted cell proliferation of MM through inhibiting T cell immune responses via PD-1/PD-L1 pathway.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsB7-H1 AntigenBone Marrow CellsCell ProliferationCoculture TechniquesCytokinesDisease Models, AnimalFemaleLymphocyte ActivationMesenchymal Stem CellsMesenchymal Stem Cell TransplantationMiceMice, Inbred C57BLMultiple MyelomaPrimary Cell CultureB7-H1 AntigenCd274 protein, mouseCytokinesPdcd1 protein, mouseProgrammed Cell Death 1 ReceptorRNA, Small Interfering5TGM1bone marrow mesenchymal stem cellsCD4+ T cellsMultiple myelomaPD-1/PD-L1

Identifiers

PMID29493401
PMCPMC6056211
OpenAlexW2789518130

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.