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The expression of ferroptosis-related genes in osteoporosis based on GEO.
Wu, L-L; Sui, Y-X; Cong, H-H; Leng, Z-Z; Jia, Y-M; Ao, S.
Afiliação
  • Wu LL; Department of Spine Surgery, Chifeng Municipal Hospital, Chifeng City, Inner Mongolia, China. 88381441@qq.com.
Eur Rev Med Pharmacol Sci ; 28(2): 463-468, 2024 Jan.
Article em En | MEDLINE | ID: mdl-38305593
ABSTRACT

OBJECTIVE:

The aim of this study was to screen the differential genes related to ferroptosis in osteoporosis patients. MATERIALS AND

METHODS:

GEO2R was used to screen the differential genes related to ferroptosis in osteoporosis patients by searching the relevant chips in the GEO database, and Spearman's correlation analysis was used to describe the correlation between quantitative variables without normal distribution. p-values lower than 0.05 were considered statistically significant. Another group of osteoporosis patients was selected in the GEO database to verify the significantly differentially expressed genes.

RESULTS:

The results showed that 10 samples in chip GSE35956 were identified as research objects, and a total of 5 ferroptosis differential genes were screened out ATP5MC3, CDKN1A, MT1G, NCOA4, SLC1A5, of which 3 up-regulated genes (CDKN1A, MT1G, SLC1A5), 2 down-regulated genes (ATP5MC3, NCOA4). The above differential genes were placed in 19 samples of chip GSE35959 for verification, and the same expression trend was obtained, but only the MT1G difference was statistically significant.

CONCLUSIONS:

The gene correlation test found that MT1G and ATP5MC3 had a strong negative correlation.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Osteoporose / Ferroptose Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Eur Rev Med Pharmacol Sci Assunto da revista: FARMACOLOGIA / TOXICOLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Osteoporose / Ferroptose Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Eur Rev Med Pharmacol Sci Assunto da revista: FARMACOLOGIA / TOXICOLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China