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Expression of the Circadian Clock Gene ARNTL associated with DNA repair gene and prognosis of patient with osteosarcoma.

Authors :
Kong, Daliang
Liu, Yang
Zhang, Minglei
Source :
Mutation Research: Fundamental & Molecular Mechanisms of Mutagenesis. Jul2022, Vol. 825, pN.PAG-N.PAG. 1p.
Publication Year :
2022

Abstract

The study objects were to explore the correlation between the biological role of clock genes and clinical indicators in patients with osteosarcoma (OS). We acquired the clinical information and RNA sequencing data of OS samples from the TARGET database. The protein-protein interaction (PPI) network and expression correlation analysis of clock genes were performed. Then, the functional enrichment analysis of clock genes was analyzed. The survival analysis of clock genes in patients of OS was carried out by univariate cox regression, Kaplan-Meier (KM) curve and multivariate cox regression methods. Moreover, the spearmen correlation analysis was performed to explore the correlation between clock genes and DNA repair genes in patients with OS. The PPI network and expression correlation analysis of clock genes indicated that the clock genes were highly correlated with each other. The survival analysis of clock genes found that clock gene ARNTL is a protective factor for the prognosis of patients with OS. We found that ARNTL was positively related to DNA repair genes and was involved in the biological process of DNA damage repair in patients with OS. ARNTL may affect the prognosis and chemotherapy response of patients with OS by regulating DNA repair pathways. • The clock genes were highly correlated with each other. • The clock gene ARNTL is a protective factor for the prognosis of patients with OS. • ARNTL was involved in the biological process of DNA damage repair in patients with OS. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00275107
Volume :
825
Database :
Academic Search Index
Journal :
Mutation Research: Fundamental & Molecular Mechanisms of Mutagenesis
Publication Type :
Academic Journal
Accession number :
160582729
Full Text :
https://doi.org/10.1016/j.mrfmmm.2022.111801