Evidence map›Paper›PMID 38665430›Full record

ArticleFrontiers in cell and developmental biology2024

Prognosis and therapeutic significance of IGF-1R-related signaling pathway gene signature in glioma.

Zhen Liu, Liangwang Yang, Wenqi Wu, Zejun Chen, Zhengxing Xie, Daoming Shi, Ning Cai, Shenghua Zhuo

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

11 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

8 authors at 3 institutions in 1 country.

Zhen Liu *Department of Neurosurgery, Affiliated Hospital of Jiangsu University, Zhenjiang, Jiangsu, China.
Liangwang Yang *Department of Neurosurgery, First Affiliated Hospital of Hainan Medical University, Haikou, Hainan, China.
Wenqi Wu *Department of Neurology, Affiliated Hospital of Jiangsu University, Zhenjiang, Jiangsu, China.
Zejun ChenDepartment of Neurosurgery, Affiliated Hospital of Jiangsu University, Zhenjiang, Jiangsu, China.
Zhengxing XieDepartment of Neurosurgery, Affiliated Hospital of Jiangsu University, Zhenjiang, Jiangsu, China.
Daoming ShiDepartment of General Surgery, Affiliated Hospital of Jiangsu University, Zhenjiang, Jiangsu, China.
Ning CaiDepartment of Neurosurgery, Affiliated Hospital of Jiangsu University, Zhenjiang, Jiangsu, China.
Shenghua ZhuoDepartment of Neurosurgery, First Affiliated Hospital of Hainan Medical University, Haikou, Hainan, China.
Jiangsu University · CNAffiliated Hospital of Jiangsu University · CNHainan Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Glioma is the most common cancer of the central nervous system with poor therapeutic response and clinical prognosis. Insulin-like growth factor 1 receptor ( Methods: LASSO-Cox regression was employed to develop a 16-gene risk signature in the TCGA-GBMLGG cohort, and all patients with glioma were divided into low-risk and high-risk subgroups. The relationships between the risk signature and the tumor immune microenvironment (TIME), immunotherapy response, and chemotherapy response were then analyzed. Immunohistochemistry was used to evaluate the HSP90B1 level in clinical glioma tissue. Results: The gene risk signature yielded superior predictive efficacy in prognosis (5-year area under the curve: 0.875) and can therefore serve as an independent prognostic indicator in patients with glioma. The high-risk subgroup exhibited abundant immune infltration and elevated immune checkpoint gene expression within the TIME. Subsequent analysis revealed that patients in the high-risk subgroup benefited more from chemotherapy. Immunohistochemical analysis confirmed that HSP90B1 was overexpressed in glioma, with significantly higher levels observed in glioblastoma than in astrocytoma or oligodendrocytoma. Conclusion: The newly identified 16-gene risk signature demonstrates a robust predictive capacity for glioma prognosis and plays a pivotal role in the TIME, thereby offering valuable insights for the exploration of novel biomarkers and targeted therapeutics.

Indexed as

gliomaHSP90B1IGF-1R signalingimmunotherapy/chemotherapy responsetumor immune microenvironment

Identifiers

PMID38665430
PMCPMC11043541
OpenAlexW4394723126

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.