دورية أكاديمية
CRISPR screens in mechanism and target discovery for AML
العنوان: | CRISPR screens in mechanism and target discovery for AML |
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المؤلفون: | Tian Lin, Dan Liu, Zhangchun Guan, Xuan Zhao, Sijin Li, Xu Wang, Rui Hou, Junnian Zheng, Jiang Cao, Ming Shi |
المصدر: | Heliyon, Vol 10, Iss 8, Pp e29382- (2024) |
بيانات النشر: | Elsevier, 2024. |
سنة النشر: | 2024 |
المجموعة: | LCC:Science (General) LCC:Social sciences (General) |
مصطلحات موضوعية: | CRISPR screens, AML, Therapeutic targets, Mechanism, Science (General), Q1-390, Social sciences (General), H1-99 |
الوصف: | CRISPR-based screens have discovered novel functional genes involving in diverse tumor biology and elucidated the mechanisms of the cancer pathological states. Recently, with its randomness and unbiasedness, CRISPR screens have been used to discover effector genes with previously unknown roles for AML. Those novel targets are related to AML survival resembled cellular pathways mediating epigenetics, synthetic lethality, transcriptional regulation, mitochondrial and energy metabolism. Other genes that are crucial for pharmaceutical targeting and drug resistance have also been identified. With the rapid development of novel strategies, such as barcodes and multiplexed mosaic CRISPR perturbation, more potential therapeutic targets and mechanism in AML will be discovered. In this review, we present an overview of recent progresses in the development of CRISPR-based screens for the mechanism and target identification in AML and discuss the challenges and possible solutions in this rapidly growing field. |
نوع الوثيقة: | article |
وصف الملف: | electronic resource |
اللغة: | English |
تدمد: | 2405-8440 |
Relation: | http://www.sciencedirect.com/science/article/pii/S2405844024054136; https://doaj.org/toc/2405-8440 |
DOI: | 10.1016/j.heliyon.2024.e29382 |
URL الوصول: | https://doaj.org/article/1681110421ae473aa1a9da32d8de390d |
رقم الأكسشن: | edsdoj.1681110421ae473aa1a9da32d8de390d |
قاعدة البيانات: | Directory of Open Access Journals |
تدمد: | 24058440 |
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DOI: | 10.1016/j.heliyon.2024.e29382 |