Evidence map›Paper›PMID 35842634›Full record

ReviewJournal of translational medicine2022

TA-MSCs, TA-MSCs-EVs, MIF: their crosstalk in immunosuppressive tumor microenvironment.

Zhenghou Zhang, Xiangyu Zhou, Jinshuai Guo, Fusheng Zhang, Yiping Qian, Guang Wang, Meiqi Duan, Yutian Wang, Haiying Zhao, Zhi Yang and 2 more

Open access · goldAbstract readReview
In one paragraph

Review in Journal of translational medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

20 citing papers in PubMed, 20 citations in OpenAlex.

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  17. Cell death shapes cancer immunity: spotlighting PANoptosis.Journal of experimental & clinical cancer research : CR · 2024
    Review
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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

12 authors at 1 institution in 1 country.

Zhenghou Zhang *Department of General Surgery, The Fourth Affiliated Hospital of China Medical University, Shenyang, Liaoning, China.
Xiangyu Zhou *Department of General Surgery, The Fourth Affiliated Hospital of China Medical University, Shenyang, Liaoning, China.
Jinshuai GuoDepartment of General Surgery, The Fourth Affiliated Hospital of China Medical University, Shenyang, Liaoning, China.
Fusheng ZhangDepartment of General Surgery, The Fourth Affiliated Hospital of China Medical University, Shenyang, Liaoning, China.
Yiping QianDepartment of General Surgery, The Fourth Affiliated Hospital of China Medical University, Shenyang, Liaoning, China.
Guang WangDepartment of General Surgery, The Fourth Affiliated Hospital of China Medical University, Shenyang, Liaoning, China.
Meiqi DuanDepartment of General Surgery, The Fourth Affiliated Hospital of China Medical University, Shenyang, Liaoning, China.
Yutian WangDepartment of General Surgery, The Fourth Affiliated Hospital of China Medical University, Shenyang, Liaoning, China.
Haiying ZhaoDepartment of General Surgery, The Fourth Affiliated Hospital of China Medical University, Shenyang, Liaoning, China.
Zhi YangDepartment of General Surgery, The Fourth Affiliated Hospital of China Medical University, Shenyang, Liaoning, China.
Zunpeng LiuDepartment of Orthopedics, The Fourth Affiliated Hospital of China Medical University, Shenyang, China. zp_liu@126.com.
Xiaofeng JiangDepartment of General Surgery, The Fourth Affiliated Hospital of China Medical University, Shenyang, Liaoning, China. 18900912171@163.com.ORCID 0000-0002-5483-8111
Fourth Affiliated Hospital of China Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As an important component of the immunosuppressive tumor microenvironment (TME), it has been established that mesenchymal stem cells (MSCs) promote the progression of tumor cells. MSCs can directly promote the proliferation, migration, and invasion of tumor cells via cytokines and chemokines, as well as promote tumor progression by regulating the functions of anti-tumor immune and immunosuppressive cells. MSCs-derived extracellular vesicles (MSCs-EVs) contain part of the plasma membrane and signaling factors from MSCs; therefore, they display similar effects on tumors in the immunosuppressive TME. The tumor-promoting role of macrophage migration inhibitory factor (MIF) in the immunosuppressive TME has also been revealed. Interestingly, MIF exerts similar effects to those of MSCs in the immunosuppressive TME. In this review, we summarized the main effects and related mechanisms of tumor-associated MSCs (TA-MSCs), TA-MSCs-EVs, and MIF on tumors, and described their relationships. On this basis, we hypothesized that TA-MSCs-EVs, the MIF axis, and TA-MSCs form a positive feedback loop with tumor cells, influencing the occurrence and development of tumors. The functions of these three factors in the TME may undergo dynamic changes with tumor growth and continuously affect tumor development. This provides a new idea for the targeted treatment of tumors with EVs carrying MIF inhibitors.

Indexed as

Extracellular VesiclesMacrophage Migration-Inhibitory FactorsMesenchymal Stem CellsNeoplasmsHumansIntramolecular OxidoreductasesTumor MicroenvironmentIntramolecular OxidoreductasesMacrophage Migration-Inhibitory FactorsMIF protein, humanAnti-tumor immune cellsExtracellular vesiclesImmunosuppressive cellsImmunosuppressive tumor microenvironmentMacrophage migration inhibitory factorTA-MSCs

Identifiers

PMID35842634
PMCPMC9287873
OpenAlexW4285587113

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.