Marilia Medical School (FAMEMA), Marilia, São Paulo, Brazil.
University of Marilia, Marilia, São Paulo, Brazil.
Cell Mol Neurobiol. 2023 Aug;43(6):2953-2962. doi: 10.1007/s10571-023-01341-9. Epub 2023 Mar 29.
Alzheimer's disease (AD) is a progressive neuroinflammatory and neurodegenerative disorder that affects different regions of the brain. Its pathophysiology includes the accumulation of β-amyloid protein, formation of neurofibrillary tangles, and inflammatory processes. Genetic factors are involved in the onset of AD, but they are not fully elucidated. Identification of gene expression in encephalic tissues of patients with AD may help elucidate its development. Our objectives were to characterize and compare the gene expression of CDK10, CDK11, FOXO1, and FOXO3 in encephalic tissue samples from AD patients and elderly controls, from the auditory cortex and cerebellum. RT-qPCR was used on samples from 82 individuals (45 with AD and 37 controls). We observed a statistically significant increase in CDK10 (p = 0.029*) and CDK11 (p = 0.048*) gene expression in the AD group compared to the control, which was most evident in the cerebellum. Furthermore, the Spearman test demonstrated the presence of a positive correlation of gene expression both in the auditory cortex in the AD group (r = 0.046/p = 0.004) and control group (r = 0.454/p = 0.005); and in the cerebellum in the AD group (r = 0.654 /p < 0.001). There was no statistically significant difference and correlation in the gene expression of FOXO1 and FOXO3 in the AD group and the control. In conclusion, CDK10 and CDK11 have high expression in AD patients compared to control, and they present a positive correlation of gene expression in the analyzed groups and tissues, which suggests that they play an important role in the pathogenesis of AD.
阿尔茨海默病(AD)是一种进行性神经炎症和神经退行性疾病,影响大脑的不同区域。其病理生理学包括β-淀粉样蛋白的积累、神经原纤维缠结的形成和炎症过程。遗传因素与 AD 的发病有关,但尚未完全阐明。鉴定 AD 患者脑内组织的基因表达可能有助于阐明其发病机制。我们的目的是表征和比较 AD 患者和老年对照组听觉皮层和小脑脑组织样本中 CDK10、CDK11、FOXO1 和 FOXO3 的基因表达。使用 RT-qPCR 对 82 个人的样本(45 名 AD 患者和 37 名对照组)进行分析。与对照组相比,我们观察到 AD 组中 CDK10(p=0.029*)和 CDK11(p=0.048*)基因表达的统计学显著增加,在小脑最为明显。此外,Spearman 检验表明 AD 组(r=0.046/p=0.004)和对照组(r=0.454/p=0.005)听觉皮层以及 AD 组(r=0.654/p<0.001)小脑内基因表达存在正相关。AD 组和对照组中 FOXO1 和 FOXO3 的基因表达没有统计学显著差异和相关性。与对照组相比,AD 患者的 CDK10 和 CDK11 表达较高,并且在分析的组和组织中存在基因表达的正相关,这表明它们在 AD 的发病机制中发挥重要作用。