DARS2 overexpression is associated with PET/CT metabolic parameters and affects glycolytic activity in lung adenocarcinoma.


Journal

Journal of translational medicine
ISSN: 1479-5876
Titre abrégé: J Transl Med
Pays: England
ID NLM: 101190741

Informations de publication

Date de publication:
26 08 2023
Historique:
received: 21 05 2023
accepted: 19 08 2023
medline: 28 8 2023
pubmed: 26 8 2023
entrez: 25 8 2023
Statut: epublish

Résumé

This study investigated the correlation between the expression of DARS2 and metabolic parameters of This study used genomics and proteomics to analyze the difference in DARS2 expression between LUAD samples and control samples. An analysis of 62 patients with LUAD who underwent DARS2 expression was significantly higher in LUAD samples than in control samples (p < 0.001). DARS2 has high specificity (98.4%) and sensitivity (95.2%) in the diagnosis of LUAD. DARS2 expression was positively correlated with SUVmax, SUVmean, and TLG (p < 0.001). At the same time, the sensitivity and specificity of SUVmax in predicting DARS2 overexpression in LUAD were 88.9% and 65.9%, respectively. In vitro cell experiments have shown that interfering with DARS2 expression can inhibit the proliferation and migration of LUAD cells, promote cell apoptosis, and inhibit the glycolytic activity of tumor cells by inhibiting the expression of glycolytic related genes SLC2A1, GPI, ALDOA, and PGAM1. Overexpression of DARS2 is associated with metabolic parameters on

Sections du résumé

BACKGROUND
This study investigated the correlation between the expression of DARS2 and metabolic parameters of
METHODS
This study used genomics and proteomics to analyze the difference in DARS2 expression between LUAD samples and control samples. An analysis of 62 patients with LUAD who underwent
RESULTS
DARS2 expression was significantly higher in LUAD samples than in control samples (p < 0.001). DARS2 has high specificity (98.4%) and sensitivity (95.2%) in the diagnosis of LUAD. DARS2 expression was positively correlated with SUVmax, SUVmean, and TLG (p < 0.001). At the same time, the sensitivity and specificity of SUVmax in predicting DARS2 overexpression in LUAD were 88.9% and 65.9%, respectively. In vitro cell experiments have shown that interfering with DARS2 expression can inhibit the proliferation and migration of LUAD cells, promote cell apoptosis, and inhibit the glycolytic activity of tumor cells by inhibiting the expression of glycolytic related genes SLC2A1, GPI, ALDOA, and PGAM1.
CONCLUSIONS
Overexpression of DARS2 is associated with metabolic parameters on

Identifiants

pubmed: 37626419
doi: 10.1186/s12967-023-04454-3
pii: 10.1186/s12967-023-04454-3
pmc: PMC10463715
doi:

Substances chimiques

Fluorodeoxyglucose F18 0Z5B2CJX4D
DARS2 protein, human EC 6.1.1.12
Aspartate-tRNA Ligase EC 6.1.1.12

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

574

Informations de copyright

© 2023. BioMed Central Ltd., part of Springer Nature.

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Auteurs

Xu-Sheng Liu (XS)

Department of Nuclear Medicine, Hubei Provincial Clinical Research Center for Umbilical Cord Blood Hematopoietic Stem Cells, Taihe Hospital, Hubei University of Medicine, Shiyan, 442000, China.

Ling-Ling Yuan (LL)

Department of Pathology, Taihe Hospital, Hubei University of Medicine, Shiyan, 442000, China.

Yan Gao (Y)

Department of Nuclear Medicine, Hubei Provincial Clinical Research Center for Umbilical Cord Blood Hematopoietic Stem Cells, Taihe Hospital, Hubei University of Medicine, Shiyan, 442000, China.

Xing Ming (X)

Department of Infection Control, Taihe Hospital, Hubei University of Medicine, Shiyan, 442000, China.

Yao-Hua Zhang (YH)

Department of Nuclear Medicine, Hubei Provincial Clinical Research Center for Umbilical Cord Blood Hematopoietic Stem Cells, Taihe Hospital, Hubei University of Medicine, Shiyan, 442000, China.

Yu Zhang (Y)

Department of Nuclear Medicine, Hubei Provincial Clinical Research Center for Umbilical Cord Blood Hematopoietic Stem Cells, Taihe Hospital, Hubei University of Medicine, Shiyan, 442000, China.

Zi-Yue Liu (ZY)

Department of Nuclear Medicine, Hubei Provincial Clinical Research Center for Umbilical Cord Blood Hematopoietic Stem Cells, Taihe Hospital, Hubei University of Medicine, Shiyan, 442000, China.

Yi Yang (Y)

Department of Nuclear Medicine, Hubei Provincial Clinical Research Center for Umbilical Cord Blood Hematopoietic Stem Cells, Taihe Hospital, Hubei University of Medicine, Shiyan, 442000, China.

Zhi-Jun Pei (ZJ)

Department of Nuclear Medicine, Hubei Provincial Clinical Research Center for Umbilical Cord Blood Hematopoietic Stem Cells, Taihe Hospital, Hubei University of Medicine, Shiyan, 442000, China. pzjzml1980@taihehospital.com.

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