Department of Genetics, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Department of Neuroscience and Regenerative Medicine, Medical College of Georgia at Augusta University, Augusta, GA 30912, USA.
Sci Adv. 2024 Jun 21;10(25):eadn8709. doi: 10.1126/sciadv.adn8709.
Androgen deprivation therapy (ADT) for prostate cancer is associated with an increased risk of dementia, including Alzheimer's disease (AD). The mechanistic connection between ADT and AD-related cognitive impairment in patients with prostate cancer remains elusive. We established a clinically relevant prostate cancer-bearing AD mouse model to explore this. Both tumor-bearing and ADT induce complex changes in immune and inflammatory responses in peripheral blood and in the brain. ADT disrupts the integrity of the blood-brain barrier (BBB) and promotes immune cell infiltration into the brain, enhancing neuroinflammation and gliosis without affecting the amyloid plaque load. Moreover, treatment with natalizumab, an FDA-approved drug targeting peripheral immune cell infiltration, reduces neuroinflammation and improves cognitive function in this model. Our study uncovers an inflammatory mechanism, extending beyond amyloid pathology, that underlies ADT-exacerbated cognitive deficits, and suggests natalizumab as a potentially effective treatment in alleviating the detrimental effects of ADT on cognition.
雄激素剥夺疗法(ADT)治疗前列腺癌与痴呆症风险增加有关,包括阿尔茨海默病(AD)。ADT 与前列腺癌患者 AD 相关认知障碍之间的机制联系仍不清楚。我们建立了一种具有临床相关性的前列腺癌荷瘤 AD 小鼠模型来对此进行探索。荷瘤和 ADT 都会引起外周血和大脑中免疫和炎症反应的复杂变化。ADT 破坏血脑屏障(BBB)的完整性,并促进免疫细胞浸润大脑,增强神经炎症和神经胶质增生,而不影响淀粉样斑块负荷。此外,用那他珠单抗(一种经 FDA 批准的靶向外周免疫细胞浸润的药物)治疗可减轻该模型中的神经炎症并改善认知功能。我们的研究揭示了一种炎症机制,该机制超出了淀粉样蛋白病理学的范围,是 ADT 加重认知缺陷的基础,并表明那他珠单抗作为一种潜在有效的治疗方法,可减轻 ADT 对认知功能的不利影响。