Evidence map›Paper›PMID 33110201›Full record

ArticleScientific reports2020

Development of a novel immune-related genes prognostic signature for osteosarcoma.

Zuo-Long Wu, Ya-Jun Deng, Guang-Zhi Zhang, En-Hui Ren, Wen-Hua Yuan, Qi-Qi Xie

Abstract read
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Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

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25citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

25 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

6 authors.

Zuo-Long WuGuanghe Traditional Chinese and Western Medicine Hospital, Lanzhou, 730000, Gansu, China.
Ya-Jun DengDepartment of Orthopaedics, Second Hospital of Lanzhou University, Lanzhou, 730000, Gansu, China.
Guang-Zhi ZhangDepartment of Orthopaedics, Second Hospital of Lanzhou University, Lanzhou, 730000, Gansu, China.
En-Hui RenBreast Disease Diagnosis and Treatment Center, Affiliated Hospital of Qinghai University & Affiliated Cancer Hospital of Qinghai University, No.29 Tongren Road, Xining, 810000, Qinghai, China.
Wen-Hua YuanDepartment of Orthopaedics, Second Hospital of Lanzhou University, Lanzhou, 730000, Gansu, China.
Qi-Qi XieBreast Disease Diagnosis and Treatment Center, Affiliated Hospital of Qinghai University & Affiliated Cancer Hospital of Qinghai University, No.29 Tongren Road, Xining, 810000, Qinghai, China. jieqq16@lzu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immune-related genes (IRGs) are responsible for osteosarcoma (OS) initiation and development. We aimed to develop an optimal IRGs-based signature to assess of OS prognosis. Sample gene expression profiles and clinical information were downloaded from the Therapeutically Applicable Research to Generate Effective Treatments (TARGET) and Genotype-Tissue Expression (GTEx) databases. IRGs were obtained from the ImmPort database. R software was used to screen differentially expressed IRGs (DEIRGs) and functional correlation analysis. DEIRGs were analyzed by univariate Cox regression and iterative LASSO Cox regression analysis to develop an optimal prognostic signature, and the signature was further verified by independent cohort (GSE39055) and clinical correlation analysis. The analyses yielded 604 DEIRGs and 10 hub IRGs. A prognostic signature consisting of 13 IRGs was constructed, which strikingly correlated with OS overall survival and distant metastasis (p < 0.05, p < 0.01), and clinical subgroup showed that the signature's prognostic ability was independent of clinicopathological factors. Univariate and multivariate Cox regression analyses also supported its prognostic value. In conclusion, we developed an IRGs signature that is a prognostic indicator in OS patients, and the signature might serve as potential prognostic indicator to identify outcome of OS and facilitate personalized management of the high-risk patients.

Indexed as

Gene Expression Regulation, NeoplasticBiomarkers, TumorCohort StudiesFemaleHumansKaplan-Meier EstimateMaleOsteosarcomaPrognosisBiomarkers, Tumor

Identifiers

PMID33110201
PMCPMC7591524

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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.