Evidence map›Paper›PMID 35602303›Full record

ArticleJournal of oncology2022

Development of a Risk Score Model for Osteosarcoma Based on DNA Methylation-Driven Differentially Expressed Genes.

Yuxiang Kang, Guowang Li, Guohua Wang, Zhenxin Huo, Xiangling Feng, Lilong Du, Yongjin Li, Qiang Yang, Xinlong Ma, Bingbing Yu and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 39% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
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

11 authors at 3 institutions in 1 country.

Yuxiang KangDepartment of Minimally Invasive Spine Surgery, Tianjin Hospital, Tianjin, China.ORCID https://orcid.org/0000-0002-2706-2901
Guowang LiGraduate School of Tianjin Medical University, Tianjin, China.
Guohua WangGraduate School of Tianjin Medical University, Tianjin, China.
Zhenxin HuoGraduate School of Tianjin Medical University, Tianjin, China.
Xiangling FengDepartment of Pharmacology, Tianjin Key Laboratory of Inflammation Biology, School of Basic Medical Sciences, Tianjin Medical University, Tianjin, China.
Lilong DuDepartment of Minimally Invasive Spine Surgery, Tianjin Hospital, Tianjin, China.
Yongjin LiGraduate School of Tianjin Medical University, Tianjin, China.
Qiang YangDepartment of Minimally Invasive Spine Surgery, Tianjin Hospital, Tianjin, China.
Xinlong MaDepartment of Minimally Invasive Spine Surgery, Tianjin Hospital, Tianjin, China.
Bingbing YuDepartment of Orthopedics, The Fifth Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.ORCID https://orcid.org/0000-0001-9092-3711
Baoshan XuDepartment of Minimally Invasive Spine Surgery, Tianjin Hospital, Tianjin, China.ORCID https://orcid.org/0000-0002-4407-8745
Tianjin Hospital · CNTianjin Medical University · CNGuangzhou Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteosarcoma (OS) is the commonest malignant bone tumor in adolescent patients, and patients face amputation, tumor metastasis, chemotherapy resistance, and even death. We investigated the potential connection between abnormal methylation differentially expressed genes and the survival rate of osteosarcoma patients. GSE36002 and GSE12865 datasets of GEO database were utilized for abnormal methylation differentially expressed genes, followed by function and pathway enrichment analyses, the protein-protein interaction network in the STRING database, and cluster analysis in the MCODE app of Cytoscape. The RNA-seq and clinical data from the TARGET-OS project of TCGA were used for univariate and least absolute shrinkage and selection operator (LASSO) Cox regression analyses to predict the risk genes of osteosarcoma. 1191 hypermethylation-downregulated genes might function through plasma membrane, negative regulation of transcription from the RNA polymerase II promoter, and pathways, including transcriptional misregulation in cancer. 127 hypomethylation-upregulated genes were enriched in proteolysis, negative regulation of the canonical Wnt signaling pathway, and metabolic signaling pathways. The univariate Cox analysis revealed 638 genes (

Identifiers

PMID35602303
PMCPMC9122702
OpenAlexW4280540017

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.