Evidence map›Paper›PMID 34691083›Full record

ArticleFrontiers in immunology2021

Low GNG12 Expression Predicts Adverse Outcomes: A Potential Therapeutic Target for Osteosarcoma.

Jinghong Yuan, Zhao Yuan, Aifang Ye, Tianlong Wu, Jingyu Jia, Jia Guo, Jian Zhang, Tao Li, Xigao Cheng

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

13 citing papers in PubMed, 17 citations in OpenAlex.

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  7. American journal of cancer research · 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

9 authors at 3 institutions in 1 country.

Jinghong YuanDepartment of Orthopaedics, The Second Affiliated Hospital of Nanchang University, Nanchang, China.
Zhao YuanClinical Research Center, The Second Affiliated Hospital of Nanchang University, Nanchang, China.
Aifang YeDepartment of Otorhinolaryngology, Jiangxi Provincial Children's Hospital, Nanchang, China.
Tianlong WuInstitute of Orthopaedics of Jiangxi Province, Nanchang, China.
Jingyu JiaInstitute of Minimally Invasive Orthopaedics of Nanchang University, Nanchang University, Nanchang, China.
Jia GuoDepartment of Orthopaedics, Jiangxi Provincial People's Hospital Affiliated to Nanchang University, Nanchang, China.
Jian ZhangDepartment of Orthopaedics, The Second Affiliated Hospital of Nanchang University, Nanchang, China.
Tao LiDepartment of Orthopaedics, The Second Affiliated Hospital of Nanchang University, Nanchang, China.
Xigao ChengDepartment of Orthopaedics, The Second Affiliated Hospital of Nanchang University, Nanchang, China.
Second Affiliated Hospital of Nanchang University · CNNanchang University · CNJiangxi Provincial Children's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: G protein subunit gamma 12 (GNG12) is observed in some types of cancer, but its role in osteosarcoma is unknown. This study hypothesized that GNG12 may be a potential biomarker and therapeutic target. We aimed to identify an association between GNG12 and osteosarcoma based on the Gene Expression Omnibus and the Therapeutically Applicable Research to Generate Effective Treatments (TARGET) databases. Methods: Osteosarcoma samples in GSE42352 and TARGET database were selected as the test cohorts. As the external validation cohort, 78 osteosarcoma specimens from The Second Affiliated Hospital of Nanchang University were collected. Patients with osteosarcoma were divided into high and low GNG12 mRNA-expression groups; differentially expressed genes were identified as GNG12-related genes. The biological function of GNG12 was annotated using Gene Ontology, Kyoto Encyclopedia of Genes and Genomes, gene set enrichment analysis, and immune infiltration analysis. Gene expression correlation analysis and competing endogenous RNA regulatory network construction were used to determine potential biological regulatory relationships of GNG12. Overall survival, Kaplan-Meier analysis, and log-rank tests were calculated to determine GNG12 reliability in predicting survival prognosis. Results: GNG12 expression decreased in osteosarcoma samples. GNG12 was a highly effective biomarker for osteosarcoma [area under the receiver operating characteristic (ROC) curve (AUC) = 0.920], and the results of our Kaplan-Meier analysis indicated that overall survival and progression-free survival differed significantly between low and high GNG-expression group (p < 0.05). Functional analyses indicated that GNG12 may promote osteosarcoma through regulating the endoplasmic reticulum. Expression correlation analysis and competing endogenous RNA network construction showed that HOTTIP/miR-27a-3p may regulate GNG12 expression. Furthermore, the subunit suppresses adaptive immunity Conclusion: This study identified GNG12 as a potential biomarker for osteosarcoma prognosis, highlighting its potential as an immunotherapy target.

Indexed as

Biomarkers, TumorBone NeoplasmsGTP-Binding Protein gamma SubunitsHumansMacrophagesMast CellsOsteosarcomaTumor MicroenvironmentBiomarkers, TumorGNG12 protein, humanGTP-Binding Protein gamma SubunitsbiomarkerGNG12osteosarcomaprognosistherapeutic target

Identifiers

PMID34691083
PMCPMC8527884
OpenAlexW3201913425

What OpenQuestion 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 OpenQuestion graph.