Evidence map›Paper›PMID 37928523›Full record

ArticleFrontiers in immunology2023

IGFBP2 from a novel copper metabolism-associated biomarker promoted glioma progression and response to immunotherapy.

Qisheng Luo, Junhong Zhuang, Dandan Zheng, Changfeng Miao, Hongcheng Luo, Jun Peng, Chuanhua Zheng, Chengjian Qin, Chuanliu Lan, Meiqin Chen and 3 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

8 citing papers in PubMed, 7 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 6 institutions in 1 country.

Qisheng LuoDepartment of Neurosurgery, Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, Guangxi, China.
Junhong ZhuangDepartment of Neurology, Affiliated Haikou Hospital of Xiangya Medical School, Central South University, Haikou, China.
Dandan ZhengDepartment of Radiation Oncology, The First Affiliated Hospital Zhejiang University, Hangzhou, China.
Changfeng MiaoDepartment of Laboratory Medicine, Neurosurgery Second Branche, Hunan Provincial People's Hospital (The First affiliated Hospital of Hunan Normal University), Changsha, Hunan, China.
Hongcheng LuoDepartment of Laboratory Medicine, Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, Guangxi, China.
Jun PengDepartment of Neurosurgery, Affiliated Haikou Hospital of Xiangya Medical School, Central South University, Haikou, China.
Chuanhua ZhengDepartment of Neurosurgery, Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, Guangxi, China.
Chengjian QinDepartment of Neurosurgery, Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, Guangxi, China.
Chuanliu LanDepartment of Neurosurgery, Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, Guangxi, China.
Meiqin ChenDepartment of Radiation Oncology, Affiliated Jinhua Hospital, Zhejiang University School of Medicine, Jinhua, Zhejiang, China.
Ying XiaDepartment of Neurosurgery, Affiliated Haikou Hospital of Xiangya Medical School, Central South University, Haikou, China.
Deyou HuangDepartment of Radiology, Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, Guangxi, China.
Zigui ChenDepartment of Neurosurgery, Affiliated Haikou Hospital of Xiangya Medical School, Central South University, Haikou, China.
Affiliated Hospital of Youjiang Medical University for Nationalities · CNCentral South University · CNFirst Affiliated Hospital Zhejiang University · CNHainan Medical University · CNHunan Provincial People's Hospital · CNZhejiang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Copper metabolism encompasses all cellular metabolic processes involving copper ions and plays a significant role in the pathogenesis of diseases, including cancer. Furthermore, copper is intricately involved in various processes related to nucleotide metabolism. However, a comprehensive analysis of copper metabolism in gliomas remains lacking despite its importance. Methods: To address this gap, glioma patients were stratified based on the expression levels of copper metabolism-related genes. By utilizing machine learning techniques, a novel copper metabolism-associated biomarker was developed. The potential of this biomarker in prognosis, mutation analysis, and predicting immunotherapy response efficiency in gliomas was systematically investigated. Results: Notably, IGFBP2, identified as a glioma tumor promoter, was found to promote disease progression and influence immunotherapy response. Additionally, glioma-derived IGFBP2 was observed to enhance microglial migration. High IGFBP2 expression in GBM cells facilitated macrophage interactions through the EGFR, CD63, ITGB1, and CD44 signaling pathways. Discussion: Overall, the copper metabolism-associated biomarker shows promising potential to enhance the clinical management of gliomas, offering valuable insights into disease prognosis and treatment strategies.

Indexed as

Brain NeoplasmsGliomaBiomarkersCopperHumansImmunotherapyBiomarkersCoppercopper metabolismgliomasIGFBP2immunotherapynucleotide metabolism

Identifiers

PMID37928523
PMCPMC10620745
OpenAlexW4387779688

What Socratic 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 Socratic graph.