Evidence map›Paper›PMID 35402580›Full record

ArticleAnnals of translational medicine2022

Risk score model of autophagy-related genes in osteosarcoma.

Mingyang Jiang, Dalang Fang, Xiaoyu He, Jie Huang, Yang Hu, Mingjing Xie, Yiji Jike, Zhandong Bo, Wentao Qin

Open access · diamondAbstract read
In one paragraph

Article in Annals of translational medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 49% 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

3 citing papers in PubMed, 4 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

9 authors at 4 institutions in 1 country.

Mingyang Jiang *Department of Bone and Joint Surgery, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Dalang Fang *Department of Breast and Thyroid Surgery, The Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, China.
Xiaoyu He *Department of Thoracic Surgery, The Shenzhen Bao'an District Songgang People's Hospital, Shenzhen, China.
Jie HuangDepartment of Bone and Joint Surgery, The Second Affiliated Hospital of Guangxi Medical University, Nanning, China.
Yang HuDepartment of Bone and Joint Surgery, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Mingjing XieDepartment of Bone and Joint Surgery, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Yiji JikeDepartment of Bone and Joint Surgery, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Zhandong BoDepartment of Bone and Joint Surgery, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Wentao QinDepartment of Bone and Joint Surgery, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Guangxi Medical University · CNFirst Affiliated Hospital of GuangXi Medical University · CNAffiliated Hospital of Youjiang Medical University for Nationalities · CNShenzhen Bao'an District People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Osteosarcoma (OS) is a common pediatric malignancy with high mortality and disability rates. Autophagy is an essential process in regulating the apoptosis and invasion of tumor cells, so constructing a risk score model of OS autophagy-related genes (ARGs) will bring benefit to the evaluation of both treatment and prognosis. Methods: We downloaded a dataset of OS from the Therapeutically Applicable Research To Generate Effective Treatments (TARGET) database, and found OS-related ARGs through the Human Autophagy Database (HADb). Five hub ARGs ( Results: Based on the five hub ARGs, we established a risk score model related to OS. High accuracy and validity were demonstrated by datasets downloaded from the GEO. The five ARGs played a role in the PI3K and MAPK pathways. Results from targeted drug sensitivity analyses were consistent with pathway analyses. Immunohistochemistry demonstrated that the expression differences of the five ARGs were significant between the OS group and the paracancerous group. Conclusions: We constructed a risk score model related to autophagy of OS, explored the diagnostic value of ARGs, and present possible therapeutic targets.

Indexed as

Autophagy genesosteosarcoma (OS)risk prediction model

Identifiers

PMID35402580
PMCPMC8987880
OpenAlexW4220826249

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.