Evidence map›Paper›PMID 36430219›Full record

ArticleInternational journal of molecular sciences2022

GDPD5 Related to Lipid Metabolism Is a Potential Prognostic Biomarker in Neuroblastoma.

Tengling Luo, Junwei Peng, Qijun Li, Yao Zhang, Yun Huang, Lei Xu, Genling Yang, Dongmei Tan, Qian Zhang, Yi Tan

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 20% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 9 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

10 authors at 2 institutions in 1 country.

Tengling LuoLaboratory Animal Center, Chongqing Medical University, Chongqing 400016, China.
Junwei PengMinistry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Pediatrics, Department of Pediatric Surgical Oncology, National Clinical Research Center for Child Health and Disorders, China International Science and Technology Cooperation Base of Child Development and Critical Disorders, Children's Hospital of Chongqing Medical University, Chongqing 400016, China.
Qijun LiLaboratory Animal Center, Chongqing Medical University, Chongqing 400016, China.
Yao ZhangLaboratory Animal Center, Chongqing Medical University, Chongqing 400016, China.
Yun HuangLaboratory Animal Center, Chongqing Medical University, Chongqing 400016, China.
Lei XuLaboratory Animal Center, Chongqing Medical University, Chongqing 400016, China.
Genling YangLaboratory Animal Center, Chongqing Medical University, Chongqing 400016, China.
Dongmei TanLaboratory Animal Center, Chongqing Medical University, Chongqing 400016, China.
Qian ZhangLaboratory Animal Center, Chongqing Medical University, Chongqing 400016, China.
Yi TanLaboratory Animal Center, Chongqing Medical University, Chongqing 400016, China.
Chongqing Medical University · CNChildren's Hospital of Chongqing Medical University · CN

Funding

Chongqing Medical University Science Foundation R16003Scientific and Technological Research Program of Chongqing Municipal Education Commission KJQN202100411
6 · The paper itself

Abstract

Neuroblastoma (NB) is an extracranial solid tumor in children with poor prognosis in high-risk patients and its pathogenesis and prognostic markers urgently need to be explored. This study aimed to explore potential biomarkers related to NB from the aspect of lipid metabolism. Fifty-eight lipid metabolism-related differentially expressed genes between high-risk NB and non-high-risk NB in the GSE49710 dataset were analyzed using bioinformatics, including 45 down-regulated genes and 13 up-regulated genes. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis identified steroid hormone biosynthesis as an abnormal metabolic pathway in high-risk NB. Survival analysis established a three-gene prognostic model, including ACHE, GDPD5 and PIK3R1. In the test data, the AUCs of the established prognostic models used to predict patient survival at 1, 3 and 5 years were 0.84, 0.90 and 0.91, respectively. Finally, in the SH-SY5Y cell line, it was verified that overexpression of GDPD5 can inhibit cell proliferation and migration, as well as affect the lipid metabolism of SH-SY5Y, but not the sugar metabolism. hsa-miR-592 was predicted to be a potential target miRNA of GDPD5 by bioinformatics. In conclusion, this study develops a lipid-metabolism-related gene-based prognostic model for NB and demonstrates that GDPD5 inhibits SH-SY5Y proliferation and migration and may be targeted by hsa-miR-592 and inhibit SH-SY5Y fat synthesis.

Indexed as

NeuroblastomaCell ProliferationChildComputational BiologyHumansLipid MetabolismPrognosisbiomarkerGDPD5lipid metabolismneuroblastoma

Identifiers

PMID36430219
PMCPMC9695425
OpenAlexW4308723238

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.