Androgen deprivation therapy exacerbates Alzheimer's-associated cognitive decline via increased brain immune cell infiltration.
Chao ZhangMae AidaShalini SagguHaiyan YuLianna ZhouHasibur RehmanKai JiaoRunhua LiuLizhong WangQin WangPublished in: Science advances (2024)
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.
Keyphrases
- prostate cancer
- cognitive decline
- mild cognitive impairment
- cognitive impairment
- white matter
- radical prostatectomy
- multiple sclerosis
- cerebral ischemia
- peripheral blood
- resting state
- mouse model
- traumatic brain injury
- blood brain barrier
- functional connectivity
- coronary artery disease
- lps induced
- emergency department
- bone marrow
- brain injury
- combination therapy
- subarachnoid hemorrhage
- inflammatory response