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CDK10, CDK11, FOXO1, and FOXO3 Gene Expression in Alzheimer's Disease Encephalic Samples
Bruno Mari Fredi1, Roger Willian De Labio2, Lucas Trevizani Rasmussen2
1Marilia Medical School (FAMEMA), Marilia, São Paulo, Brazil. bruno.fredi@famema.br.
Alzheimer's disease (AD) involves altered gene expression. Researchers found increased CDK10 and CDK11 gene expression in brain tissues of AD patients, suggesting their role in AD development.
Area of Science:
- Neuroscience
- Genetics
- Molecular Biology
Background:
- Alzheimer's disease (AD) is a progressive neurodegenerative disorder characterized by neuroinflammation and the accumulation of β-amyloid and tau pathology.
- The precise genetic factors contributing to AD pathogenesis remain incompletely understood.
- Investigating gene expression in brain tissues offers insights into AD development.
Purpose of the Study:
- To compare the gene expression of CDK10, CDK11, FOXO1, and FOXO3 in the auditory cortex and cerebellum of Alzheimer's disease patients and elderly controls.
- To identify potential genetic markers associated with AD development.
Main Methods:
- Gene expression analysis using quantitative real-time polymerase chain reaction (RT-qPCR).
- Samples were obtained from 82 individuals: 45 with AD and 37 age-matched controls.
- Statistical analyses included comparative analysis and Spearman correlation tests.
Main Results:
- A statistically significant increase in CDK10 and CDK11 gene expression was observed in the AD group compared to controls, particularly in the cerebellum.
- Positive correlations in gene expression for CDK10 and CDK11 were found in both AD and control groups within the auditory cortex and cerebellum.
- No significant differences or correlations were found for FOXO1 and FOXO3 gene expression between the groups.
Conclusions:
- CDK10 and CDK11 exhibit elevated expression in Alzheimer's disease patients.
- The positive correlation of CDK10 and CDK11 gene expression suggests their involvement in the pathogenesis of Alzheimer's disease.
- FOXO1 and FOXO3 do not appear to play a significant role in the studied AD cohort based on gene expression levels.
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