Evidence map›Paper›PMID 39654890›Full record

ArticleFrontiers in immunology2024

Exploring osteosarcoma based on the tumor microenvironment.

Ao Wu, Zhi-Kai Yang, Peng Kong, Peng Yu, You-Tong Li, Jia-le Xu, Si-Shan Bian, Jia-Wen Teng

Abstract read
In one paragraph

Article in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. [Bioinformatics analysis of oxidative stress and immune infiltration in rheumatoid arthritis].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2025
    Article
  4. Review
  5. Review
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.

Ao WuThe First Clinical College of Shandong University of Traditional Chinese Medicine, Jinan, Shandong, China.
Zhi-Kai YangHand and Foot Orthopaedic Department, Changle County People's Hospital, Weifang, Shandong, China.
Peng KongDepartment of Minimally Invasive Orthopedics, Affiliated Hospital of Shandong Traditional Chinese Medicine University, Jinan, Shandong, China.
Peng YuThe First Clinical College of Shandong University of Traditional Chinese Medicine, Jinan, Shandong, China.
You-Tong LiThe First Clinical College of Shandong University of Traditional Chinese Medicine, Jinan, Shandong, China.
Jia-le XuThe First Clinical College of Shandong University of Traditional Chinese Medicine, Jinan, Shandong, China.
Si-Shan BianDepartment of Traumatology and Orthopaedics, Affiliated Hospital of Shandong University of Traditional Chinese Medicine, Jinan, Shandong, China.
Jia-Wen TengDepartment of Traumatology and Orthopaedics, Affiliated Hospital of Shandong University of Traditional Chinese Medicine, Jinan, Shandong, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteosarcoma is a cancerous bone tumor that develops from mesenchymal cells and is characterized by early metastasis, easy drug resistance, high disability, and mortality. Immunological characteristics of the tumor microenvironment (TME) have attracted attention for the prognosis and treatment of osteosarcoma, and there is a need to explore a signature with high sensitivity for prognosis. In the present study, a total of 84 samples of osteosarcoma were acquired from the UCSC Xena database, analyzed for immune infiltration and classified into two categories depending on their immune properties, and then screened for DEGs between the two groups and analyzed for enrichment, with the majority of DEGs enriched in the immune domain. To further analyze their immune characteristics, the immune-related genes were obtained from the TIMER database. We performed an intersection analysis to identify immune-related differentially expressed genes (IR-DEGs), which were analyzed using a univariate COX regression, and LASSO analysis was used to obtain the ideal genes to construct the risk model, and to uncover the prognostic distinctions between high-risk scoring group and low-risk scoring group, a survival analysis was conducted. The risk assessment model developed in this study revealed a notable variation in survival analysis outcomes between the high-risk and low-risk scoring groups, and the conclusions reached by the model are consistent with the findings of previous scholars. They also yield meaningful results when analyzing immune checkpoints. The risk assessment model developed in this study is precise and dependable for forecasting outcomes and analyzing characteristics of osteosarcoma.

Indexed as

Bone NeoplasmsGene Expression Regulation, NeoplasticOsteosarcomaTumor MicroenvironmentBiomarkers, TumorComputational BiologyDatabases, GeneticGene Expression ProfilingHumansPrognosisTranscriptomeBiomarkers, Tumorimmune-related genesimmunization checkpointsimmunotherapyosteosarcomatumor microenvironment

Identifiers

PMID39654890
PMCPMC11625786

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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.