Evidence map›Paper›PMID 35111386›Full record

ArticleOncoimmunology2022

Dual role of ARPC1B in regulating the network between tumor-associated macrophages and tumor cells in glioblastoma.

Tianqi Liu, Chen Zhu, Xin Chen, Jianqi Wu, Gefei Guan, Cunyi Zou, Shuai Shen, Ling Chen, Peng Cheng, Wen Cheng and 1 more

Open access · goldAbstract read
In one paragraph

Article in Oncoimmunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

22 citing papers in PubMed, 23 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 2 countries.

Tianqi LiuDepartment of Neurosurgery, The First Hospital of China Medical University, Shenyang, Liaoning, China.
Chen ZhuDepartment of Neurosurgery, The First Hospital of China Medical University, Shenyang, Liaoning, China.
Xin ChenDepartment of Neurosurgery, The First Hospital of China Medical University, Shenyang, Liaoning, China.
Jianqi WuDepartment of Neurosurgery, The First Hospital of China Medical University, Shenyang, Liaoning, China.
Gefei GuanDepartment of Neurosurgery, The First Hospital of China Medical University, Shenyang, Liaoning, China.
Cunyi ZouDepartment of Neurosurgery, The First Hospital of China Medical University, Shenyang, Liaoning, China.
Shuai ShenDepartment of Neurosurgery, The First Hospital of China Medical University, Shenyang, Liaoning, China.
Ling ChenDepartment of Neurosurgery, Chinese People's Liberation Army of China (Pla) General Hospital, Medical School of Chinese Pla, Institute of Neurosurgery of Chinese Pla, Beijing, China.
Peng ChengDepartment of Neurosurgery, The First Hospital of China Medical University, Shenyang, Liaoning, China.
Wen ChengDepartment of Neurosurgery, The First Hospital of China Medical University, Shenyang, Liaoning, China.
Anhua WuDepartment of Neurosurgery, The First Hospital of China Medical University, Shenyang, Liaoning, China.
First Hospital of China Medical University · CNChinese PLA General Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The tumor microenvironment (TME) plays a critical role in promoting the growth and metastasis of glioblastoma (GBM). Tumor-associated macrophages (TAMs), the most abundant myeloid cells infiltrating in TME, produce proinflammatory cytokines, regulate glioma cell pools, and lead to GBM progression. Understanding the mechanism of GBM-TAMs regulation can help to find new targeted therapeutic strategies against GBM. Based on the CGGA and TCGA GBM cohorts, ARPC1B was defined as the key macrophage-associated gene with prognostic value. Higher ARPC1B expression was associated with progressive malignancy, poor outcomes and TAM infiltration. We demonstrated that macrophage-expressed ARPC1B promoted the migration, invasion, and epithelial-mesenchymal transition of glioma cells. Glioma-intrinsic ARPC1B also maintained the malignant phenotype and promoted macrophage recruitment. Positive feedback signaling between macrophages and glioma cells via ARPC1B was determined to be under control of the IFNγ-IRF2-ARPC1B axis. This study highlights the important role of ARPC1B in GBM malignancy progression and the regulation network between GBM and TAMs, suggesting ARPC1B as a novel biomarker with potential therapeutic implications.

Indexed as

GlioblastomaGliomaActin-Related Protein 2-3 ComplexCell Line, TumorHumansTumor-Associated MacrophagesTumor MicroenvironmentActin-Related Protein 2-3 ComplexARPC1B protein, humanactin cytoskeletonARPC1BGBMmacrophageTAM

Identifiers

PMID35111386
PMCPMC8803105
OpenAlexW4210377949

What OpenQuestion holds

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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.