Editorial: Multi-omics studies on aging and age-related diseases

Through LASSO regression method and Cox regression analysis, three genes GPC3, GPX3 and PRICKLE1 were identified as prognostic risk signatures for overall survival among gastric cancer patients, offering tailored diagnostic and treatment strategies for gastric cancer. In addition to cancers and AD t...

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Vydané v:Frontiers in cell and developmental biology Ročník 12; s. 1374424
Hlavní autori: Wang, He-Ping, Basisty, Nathan, Qu, Jia-Hua, Wang, Xiaoman
Médium: Journal Article
Jazyk:English
Vydavateľské údaje: Switzerland Frontiers Media SA 2024
Frontiers Media S.A
Predmet:
Age
age-related diseases
Aging
Alzheimer's disease
biomarker
Biomarkers
Brain research
cancer
Cardiovascular diseases
Cell and Developmental Biology
Conflicts of interest
Disease
Editing
Gastric cancer
Genomics
Metabolic syndrome
Metabolism
Metabolites
multi-omics
Pathology
Senescence
Writing
multi-omics
age-related diseases
cancer
aging
Alzheimer’s disease
biomarker
ISSN:2296-634X, 2296-634X
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Popis
Shrnutí:Through LASSO regression method and Cox regression analysis, three genes GPC3, GPX3 and PRICKLE1 were identified as prognostic risk signatures for overall survival among gastric cancer patients, offering tailored diagnostic and treatment strategies for gastric cancer. In addition to cancers and AD that the four articles in this Research Topic focused on, other aging processes and age-related pathologies, such as metabolic syndrome, cardiovascular diseases, frailty and others, also benefit from the development and application of multi-omic techniques (Zheng et al., 2022; Sahu et al., 2023; Zhang et al., 2023). Conflict of interest The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Bibliografia:SourceType-Scholarly Journals-1
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ObjectType-Editorial-2
ObjectType-Commentary-1
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Edited and reviewed by: Philipp Kaldis, Lund University, Sweden
These authors have contributed equally to this work
ISSN:2296-634X
2296-634X
DOI:10.3389/fcell.2024.1374424