Evidence map›Paper›PMID 25978454›Full record

ArticlePloS one2015

Identification of a 6-cytokine prognostic signature in patients with primary glioblastoma harboring M2 microglia/macrophage phenotype relevance.

Jinquan Cai, Wei Zhang, Pei Yang, Yinyan Wang, Mingyang Li, Chuanbao Zhang, Zheng Wang, Huimin Hu, Yanwei Liu, Qingbin Li and 5 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed, 2 pooled it
4.2field-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

55 citing papers in PubMed, 2 syntheses or guidelines pooled it, 78 citations in OpenAlex.

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  10. Bioinformatics Analysis and Screening of Potential Target Genes Related to the Lung Cancer Prognosis.Medical principles and practice : international journal of the Kuwait University, Health Science Centre · 2023
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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

15 authors at 5 institutions in 1 country.

Jinquan CaiDepartment of Neurosurgery, The Second Affiliated Hospital of Harbin Medical University, Harbin, China; Chinese Glioma Cooperative Group (CGCG), Beijing, China.
Wei ZhangBeijing Neurosurgical Institute, Capital Medical University, Beijing, China; Department of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, Beijing, China; Chinese Glioma Cooperative Group (CGCG), Beijing, China.
Pei YangBeijing Neurosurgical Institute, Capital Medical University, Beijing, China; Department of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, Beijing, China; Chinese Glioma Cooperative Group (CGCG), Beijing, China.
Yinyan WangBeijing Neurosurgical Institute, Capital Medical University, Beijing, China; Department of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, Beijing, China; Chinese Glioma Cooperative Group (CGCG), Beijing, China.
Mingyang LiBeijing Neurosurgical Institute, Capital Medical University, Beijing, China; Department of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, Beijing, China; Chinese Glioma Cooperative Group (CGCG), Beijing, China.
Chuanbao ZhangBeijing Neurosurgical Institute, Capital Medical University, Beijing, China; Department of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, Beijing, China; Chinese Glioma Cooperative Group (CGCG), Beijing, China.
Zheng WangBeijing Neurosurgical Institute, Capital Medical University, Beijing, China; Department of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, Beijing, China; Chinese Glioma Cooperative Group (CGCG), Beijing, China.
Huimin HuBeijing Neurosurgical Institute, Capital Medical University, Beijing, China; Chinese Glioma Cooperative Group (CGCG), Beijing, China.
Yanwei LiuBeijing Neurosurgical Institute, Capital Medical University, Beijing, China; Department of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, Beijing, China; Chinese Glioma Cooperative Group (CGCG), Beijing, China.
Qingbin LiDepartment of Neurosurgery, The Second Affiliated Hospital of Harbin Medical University, Harbin, China; Chinese Glioma Cooperative Group (CGCG), Beijing, China.
Jinchong WenDepartment of Neurosurgery, The Second Affiliated Hospital of Harbin Medical University, Harbin, China; Chinese Glioma Cooperative Group (CGCG), Beijing, China.
Bo SunDepartment of Neurosurgery, The Second Affiliated Hospital of Harbin Medical University, Harbin, China; Chinese Glioma Cooperative Group (CGCG), Beijing, China.
Xiaofeng WangDepartment of Neurosurgery, The Second Affiliated Hospital of Harbin Medical University, Harbin, China; Chinese Glioma Cooperative Group (CGCG), Beijing, China.
Tao JiangBeijing Neurosurgical Institute, Capital Medical University, Beijing, China; Beijing Institute for Brain Disorders Brain Tumor Center, Beijing, China; Department of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, Beijing, China; Chinese Glioma Cooperative Group (CGCG), Beijing, China.
Chuanlu JiangDepartment of Neurosurgery, The Second Affiliated Hospital of Harbin Medical University, Harbin, China; Chinese Glioma Cooperative Group (CGCG), Beijing, China.
Capital Medical University · CNHarbin Medical University · CNBeijing Institute of Neurosurgery · CNBeijing Tian Tan Hospital · CNSecond Affiliated Hospital of Harbin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGlioblastomas (GBM) are comprised of a heterogeneous population of tumor cells, immune cells, and extracellular matrix. Interactions among these different cell types and pro-/anti-inflammatory cytokines may promote tumor development and progression.

aimsThe objective of this study was to develop a cytokine-related gene signature to improve outcome prediction for patients with primary GBM.

methodsHere, we used Cox regression and risk-score analysis to develop a cytokine-related gene signature in primary GBMs from the whole transcriptome sequencing profile of the Chinese Glioma Genome Atlas (CGGA) database (n=105). We also examined differences in immune cell phenotype and immune factor expression between the high-risk and low-risk groups.

resultsCytokine-related genes were ranked based on their ability to predict survival in the CGGA database. The six genes showing the strongest predictive value were CXCL10, IL17R, CCR2, IL17B, IL10RB, and CCL2. Patients with a high-risk score had poor overall survival and progression-free survival. Additionally, the high-risk group was characterized by increased mRNA expression of M2 microglia/macrophage markers and elevated levels of IL10 and TGFβ1.

conclusionThe six cytokine-related gene signature is sufficient to predict survival and to identify a subgroup of primary GBM exhibiting the M2 cell phenotype.

Indexed as

AdolescentAdultAgedAged, 80 and overBrain NeoplasmsChemokine CCL2Chemokine CXCL10CytokinesDNA MethylationGlioblastomaHumansInterleukin-10 Receptor beta SubunitInterleukin-17MacrophagesMicrogliaMiddle AgedCCL2 protein, humanCCR2 protein, humanChemokine CCL2Chemokine CXCL10CXCL10 protein, humanCytokinesIL10RB protein, humanIL17B protein, humanIL17RA protein, humanInterleukin-10 Receptor beta SubunitInterleukin-17Receptors, CCR2Receptors, Interleukin-17

Identifiers

PMID25978454
PMCPMC4433225
OpenAlexW1507971298

What OpenQuestion holds

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LicenceCC BY
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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.