التفاصيل البيبلوغرافية
| العنوان: |
FOXO family isoforms |
| المؤلفون: |
Bruno F. Santos, Inês Grenho, Paulo J. Martel, Bibiana I. Ferreira, Wolfgang Link |
| المصدر: |
Cell Death and Disease, Vol 14, Iss 10, Pp 1-16 (2023) |
| بيانات النشر: |
Nature Publishing Group, 2023. |
| سنة النشر: |
2023 |
| المجموعة: |
LCC:Cytology |
| مصطلحات موضوعية: |
Cytology, QH573-671 |
| الوصف: |
Abstract FOXO family of proteins are transcription factors involved in many physiological and pathological processes including cellular homeostasis, stem cell maintenance, cancer, metabolic, and cardiovascular diseases. Genetic evidence has been accumulating to suggest a prominent role of FOXOs in lifespan regulation in animal systems from hydra, C elegans, Drosophila, and mice. Together with the observation that FOXO3 is the second most replicated gene associated with extreme human longevity suggests that pharmacological targeting of FOXO proteins can be a promising approach to treat cancer and other age-related diseases and extend life and health span. However, due to the broad range of cellular functions of the FOXO family members FOXO1, 3, 4, and 6, isoform-specific targeting of FOXOs might lead to greater benefits and cause fewer side effects. Therefore, a deeper understanding of the common and specific features of these proteins as well as their redundant and specific functions in our cells represents the basis of specific targeting strategies. In this review, we provide an overview of the evolution, structure, function, and disease-relevance of each of the FOXO family members. |
| نوع الوثيقة: |
article |
| وصف الملف: |
electronic resource |
| اللغة: |
English |
| تدمد: |
2041-4889 |
| Relation: |
https://doaj.org/toc/2041-4889 |
| DOI: |
10.1038/s41419-023-06177-1 |
| URL الوصول: |
https://doaj.org/article/da7ab7b3c62142029d99db813f088275 |
| رقم الانضمام: |
edsdoj.7ab7b3c62142029d99db813f088275 |
| قاعدة البيانات: |
Directory of Open Access Journals |
Full Text Finder