Evidence map›Paper›PMID 36983630›Full record

ArticleJournal of personalized medicine2023

Construction of Osteosarcoma Diagnosis Model by Random Forest and Artificial Neural Network.

Sheng Li, Yukang Que, Rui Yang, Peng He, Shenglin Xu, Yong Hu

Open access · goldAbstract read
In one paragraph

Article in Journal of personalized medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
4.6field-weighted citation impact, top 5% 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

14 citing papers in PubMed, 20 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

6 authors at 1 institution in 1 country.

Sheng LiDepartment of Orthopedics, First Affiliated Hospital of Anhui Medical University, Hefei 230022, China.ORCID 0000-0002-7500-6517
Yukang QueDepartment of Orthopedics, First Affiliated Hospital of Anhui Medical University, Hefei 230022, China.
Rui YangDepartment of Orthopedics, First Affiliated Hospital of Anhui Medical University, Hefei 230022, China.
Peng HeDepartment of Orthopedics, First Affiliated Hospital of Anhui Medical University, Hefei 230022, China.
Shenglin XuDepartment of Orthopedics, First Affiliated Hospital of Anhui Medical University, Hefei 230022, China.
Yong HuDepartment of Orthopedics, First Affiliated Hospital of Anhui Medical University, Hefei 230022, China.
Anhui Medical University · CN

Funding

Major projects of Natural Science Foundation of universities in Anhui Province KJ2020ZD17Program for Upgrading Basic and Clinical Collaborative Research of Anhui Medical University 2020xkjT033
6 · The paper itself

Abstract

Osteosarcoma accounts for 28% of primary bone malignancies in adults and up to 56% in children and adolescents (<20 years). However, early diagnosis and treatment are still inadequate, and new improvements are still needed. Missed diagnoses exist due to fewer traditional diagnostic methods, and clinical symptoms are often already present before diagnosis. This study aimed to develop novel and efficient predictive models for the diagnosis of osteosarcoma and to identify potential targets for exploring osteosarcoma markers. First, osteosarcoma and normal tissue expression microarray datasets were downloaded from the Gene Expression Omnibus (GEO). Then we screened the differentially expressed genes (DEGs) in the osteosarcoma and normal groups in the training group. Next, in order to explore the biologically relevant role of DEGs, Metascape and enrichment analyses were also performed on DEGs. The "randomForest" and "neuralnet" packages in R software were used to select representative genes and construct diagnostic models for osteosarcoma. The next step is to validate the model of the artificial neural network. Then, we performed an immune infiltration analysis by using the training set data. Finally, we constructed a prognostic model using representative genes for prognostic analysis. The copy number of osteosarcoma was also analyzed. A random forest classifier identified nine representative genes (ANK1, TGFBR3, TNFRSF21, HSPB8, ITGA7, RHD, AASS, GREM2, NFASC). HSPB8, RHD, AASS, and NFASC were genes we identified that have not been previously reported to be associated with osteosarcoma. The osteosarcoma diagnostic model we constructed has good performance with areas under the curves (AUCs) of 1 and 0.987 in the training and validation groups, respectively. This study opens new horizons for the early diagnosis of osteosarcoma and provides representative markers for the future treatment of osteosarcoma. This is the first study to pioneer the establishment of a genetic diagnosis model for osteosarcoma and advance the development of osteosarcoma diagnosis and treatment.

Indexed as

biomarkergene expression Omnibusneural network modelosteosarcomarandom forest classifier

Identifiers

PMID36983630
PMCPMC10056981
OpenAlexW4322742087

What OpenQuestion holds

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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.