表观基因组
清脆的
基因组编辑
计算生物学
癌症
人性化鼠标
食管癌
Cas9
生物
体内
癌症研究
基因
DNA甲基化
遗传学
基因表达
作者
Reihaneh Alsadat Mahmoudian,Moein Farshchian,Fatemeh Fardi Golyan,Parvaneh Mahmoudian,Ali Alasti,Vahid Moghimi,Mina Maftooh,Amir Avan,Seyed Mahdi Hassanian,Gordon A. Ferns,Hanie Mahaki,Soodabeh Shahidsales,Amir Avan
标识
DOI:10.1016/j.critrevonc.2023.104068
摘要
Preclinical models are extensively employed in cancer research because they can be manipulated in terms of their environment, genome, molecular biology, organ systems, and physical activity to mimic human behavior and conditions. The progress made in in vivo cancer research has resulted in significant advancements, enabling the creation of spontaneous, metastatic, and humanized mouse models. Most recently, the remarkable and extensive developments in genetic engineering, particularly the utilization of CRISPR/Cas9, transposable elements, epigenome modifications, and liquid biopsies, have further facilitated the design and development of numerous mouse models for studying cancer. In this review, we have elucidated the production and usage of current mouse models, such as xenografts, chemical-induced models, and genetically engineered mouse models (GEMMs), for studying esophageal cancer. Additionally, we have briefly discussed various gene-editing tools that could potentially be employed in the future to create mouse models specifically for esophageal cancer research.
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