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Androgen deprivation therapy exacerbates Alzheimer's-associated cognitive decline via increased brain immune cell infiltration.
Zhang, Chao; Aida, Mae; Saggu, Shalini; Yu, Haiyan; Zhou, Lianna; Rehman, Hasibur; Jiao, Kai; Liu, Runhua; Wang, Lizhong; Wang, Qin.
Afiliação
  • Zhang C; Department of Genetics, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
  • Aida M; Department of Neuroscience and Regenerative Medicine, Medical College of Georgia at Augusta University, Augusta, GA 30912, USA.
  • Saggu S; Department of Neuroscience and Regenerative Medicine, Medical College of Georgia at Augusta University, Augusta, GA 30912, USA.
  • Yu H; Department of Genetics, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
  • Zhou L; Department of Cell, Developmental, and Integrative Biology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
  • Rehman H; Department of Neuroscience and Regenerative Medicine, Medical College of Georgia at Augusta University, Augusta, GA 30912, USA.
  • Jiao K; Center for Biotechnology and Genomic Medicine, Medical College of Georgia at Augusta University, Augusta, GA 30912, USA.
  • Liu R; Department of Genetics, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
  • Wang L; Center for Clinical and Translational Science, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
  • Wang Q; Department of Genetics, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Sci Adv ; 10(25): eadn8709, 2024 Jun 21.
Article em En | MEDLINE | ID: mdl-38905345
ABSTRACT
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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Encéfalo / Barreira Hematoencefálica / Modelos Animais de Doenças / Doença de Alzheimer / Disfunção Cognitiva / Antagonistas de Androgênios Limite: Animals / Humans / Male Idioma: En Revista: Sci Adv Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Encéfalo / Barreira Hematoencefálica / Modelos Animais de Doenças / Doença de Alzheimer / Disfunção Cognitiva / Antagonistas de Androgênios Limite: Animals / Humans / Male Idioma: En Revista: Sci Adv Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos