Neurologic Surgery, Mayo Clinic, Rochester, MN 55905.
Neurosurgery, Robert Wood Johnson Medical School, Rutgers University, Piscataway, NJ 08854.
Proc Natl Acad Sci U S A. 2022 Jul 12;119(28):e2206415119. doi: 10.1073/pnas.2206415119. Epub 2022 Jul 7.
Chemotherapy-induced cognitive impairment (CICI) has emerged as a significant medical problem without therapeutic options. Using the platinum-based chemotherapy cisplatin to model CICI, we revealed robust elevations in the adenosine A receptor (AR) and its downstream effectors, cAMP and CREB, by cisplatin in the adult mouse hippocampus, a critical brain structure for learning and memory. Notably, AR inhibition by the Food and Drug Administration-approved AR antagonist KW-6002 prevented cisplatin-induced impairments in neural progenitor proliferation and dendrite morphogenesis of adult-born neurons, while improving memory and anxiety-like behavior, without affecting tumor growth or cisplatin's antitumor activity. Collectively, our study identifies AR signaling as a key pathway that can be therapeutically targeted to prevent cisplatin-induced cognitive impairments.
化疗引起的认知障碍(CICI)是一个没有治疗选择的重要医学问题。我们使用基于铂的化疗药物顺铂来模拟 CICI,发现顺铂在成年小鼠海马体中显著增加了腺苷 A 受体(AR)及其下游效应物 cAMP 和 CREB 的水平,海马体是学习和记忆的关键脑区。值得注意的是,美国食品和药物管理局批准的 AR 拮抗剂 KW-6002 抑制 AR,可防止顺铂引起的成年新生神经元祖细胞增殖和树突形态发生受损,同时改善记忆和焦虑样行为,而不影响肿瘤生长或顺铂的抗肿瘤活性。总的来说,我们的研究确定了 AR 信号作为一个关键途径,可以通过治疗靶向来预防顺铂引起的认知障碍。