Cellular mechanisms and treatments for chemobrain: insight from aging and neurodegenerative diseases

被引:112
作者
Nguyen, Lien D. [1 ,2 ]
Ehrlich, Barbara E. [1 ,2 ]
机构
[1] Yale Univ, Dept Pharmacol, New Haven, CT 06520 USA
[2] Yale Univ, Interdept Neurosci Program, New Haven, CT 06520 USA
关键词
aging; chemotherapy; cognitive impairment; neurodegenerative diseases; traumatic brain injury; BREAST-CANCER SURVIVORS; REDUCES COGNITIVE IMPAIRMENT; ALZHEIMERS-DISEASE; WHITE-MATTER; 5-FLUOROURACIL CHEMOTHERAPY; HIPPOCAMPAL NEUROGENESIS; ADULT NEUROGENESIS; PREFRONTAL CORTEX; INTRATHECAL METHOTREXATE; ENVIRONMENTAL ENRICHMENT;
D O I
10.15252/emmm.202012075
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Chemotherapy is a life-saving treatment for cancer patients, but also causes long-term cognitive impairment, or "chemobrain", in survivors. However, several challenges, including imprecise diagnosis criteria, multiple confounding factors, and unclear and heterogeneous molecular mechanisms, impede effective investigation of preventions and treatments for chemobrain. With the rapid increase in the number of cancer survivors, chemobrain is an urgent but unmet clinical need. Here, we leverage the extensive knowledge in various fields of neuroscience to gain insights into the mechanisms for chemobrain. We start by outlining why the post-mitotic adult brain is particularly vulnerable to chemotherapy. Next, through drawing comparisons with normal aging, Alzheimer's disease, and traumatic brain injury, we identify universal cellular mechanisms that may underlie the cognitive deficits in chemobrain. We further identify existing neurological drugs targeting these cellular mechanisms that can be repurposed as treatments for chemobrain, some of which were already shown to be effective in animal models. Finally, we briefly describe future steps to further advance our understanding of chemobrain and facilitate the development of effective preventions and treatments.
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页数:17
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