Evidence map›Paper›PMID 35855654›Full record

ArticleCNS neuroscience & therapeutics2022

PTX3 mediates the infiltration, migration, and inflammation-resolving-polarization of macrophages in glioblastoma.

Hao Zhang, Yifan Wang, Yihan Zhao, Tao Liu, Zeyu Wang, Nan Zhang, Ziyu Dai, Wantao Wu, Hui Cao, Songshan Feng and 3 more

Open access · goldAbstract read
In one paragraph

Article in CNS neuroscience & therapeutics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 1 pooled it
3.9field-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

37 citing papers in PubMed, 1 synthesis or guideline pooled it, 48 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

13 authors at 3 institutions in 1 country.

Hao ZhangDepartment of Neurosurgery, Xiangya Hospital, Central South University, Changsha, China.ORCID 0000-0002-4582-2556
Yifan WangDepartment of Neurosurgery, Xiangya Hospital, Central South University, Changsha, China.
Yihan ZhaoDepartment of Neurosurgery, Xiangya Hospital, Central South University, Changsha, China.
Tao LiuDepartment of Neurosurgery, Xiangya Hospital, Central South University, Changsha, China.
Zeyu WangDepartment of Neurosurgery, Xiangya Hospital, Central South University, Changsha, China.
Nan ZhangCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, China.
Ziyu DaiDepartment of Neurosurgery, Xiangya Hospital, Central South University, Changsha, China.
Wantao WuDepartment of Neurosurgery, Xiangya Hospital, Central South University, Changsha, China.
Hui CaoDepartment of Psychiatry, The Second People's Hospital of Hunan Province, The Hospital of Hunan University of Chinese Medicine, Changsha, China.
Songshan FengDepartment of Neurosurgery, Xiangya Hospital, Central South University, Changsha, China.
Liyang ZhangDepartment of Neurosurgery, Xiangya Hospital, Central South University, Changsha, China.ORCID 0000-0002-4054-1667
Quan ChengDepartment of Neurosurgery, Xiangya Hospital, Central South University, Changsha, China.ORCID 0000-0003-2401-5349
Zhixiong LiuDepartment of Neurosurgery, Xiangya Hospital, Central South University, Changsha, China.ORCID 0000-0002-0288-6306
Central South University · CNHarbin Medical University · CNSecond People Hospital of Hunan · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionPentraxin 3 (PTX3) is an essential regulator of the immune system. However, the immune-modulatory role of PTX3 in the tumor microenvironment of glioma has not been elucidated.

methodsThe RNA seq samples were obtained from The Cancer Genome Atlas (TCGA) and the China Glioma Genome Atlas (CGGA) datasets. The single-cell sequencing data of glioblastoma (GBM) samples were obtained from the Single Cell Portal platform (http://singlecell.broadinstitute.org). Immunohistochemistry was used to assess PTX3 expression, HAVCR2, PD-1, PD-L1, and CD276 in glioma sections from the Xiangya cohort (n = 60). Multiplex immunofluorescence staining of PTX3, CD68, and CD163 was performed in several solid cancer types, including GBM. HMC3 was cocultured with U251 and U87, and transwell assay and flow cytometry assay were performed to explore the migration and polarization activity of HMC3.

resultsPTX3 expression is significantly increased in GBM. PTX3 expression predicts worse survival in the Xiangya cohort. PTX3 is closely related to the expression of PD-1, PD-L1, CD276, and HAVCR2 in the tumor microenvironment. Additionally, PTX3 is involved in tumorigenic and immunogenic processes, especially the activity of macrophages based on various signaling pathways in cellular communications and critical transcription factors. Specifically, PTX3 actively mediates macrophages' infiltration, migration, and inflammation-resolving-polarization. PTX3 could also predict immunotherapy response.

conclusionPTX3 is critically involved in macrophage infiltration, migration, and inflammation-resolving-polarization and modulates an immunosuppressive microenvironment.

Indexed as

GlioblastomaGliomaB7 AntigensB7-H1 AntigenC-Reactive ProteinHumansInflammationMacrophagesPentraxinsProgrammed Cell Death 1 ReceptorSerum Amyloid P-ComponentTranscription FactorsTumor MicroenvironmentB7 AntigensB7-H1 AntigenCD276 protein, humanC-Reactive ProteinPentraxinsProgrammed Cell Death 1 ReceptorSerum Amyloid P-ComponentTranscription Factorscellular communicationglioma microenvironmentmacrophagePTX3transcription factor

Identifiers

PMID35855654
PMCPMC9532932
OpenAlexW4285900171

What OpenQuestion holds

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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.