Zebrafish models of acute leukemias: Current models and future directions.

Q1 Biochemistry, Genetics and Molecular Biology
Brandon Molina, Jasmine Chavez, Stephanie Grainger
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引用次数: 2

Abstract

Acute myeloid leukemias (AML) and acute lymphoid leukemias (ALL) are heterogenous diseases encompassing a wide array of genetic mutations with both loss and gain of function phenotypes. Ultimately, these both result in the clonal overgrowth of blast cells in the bone marrow, peripheral blood, and other tissues. As a consequence of this, normal hematopoietic stem cell function is severely hampered. Technologies allowing for the early detection of genetic alterations and understanding of these varied molecular pathologies have helped to advance our treatment regimens toward personalized targeted therapies. In spite of this, both AML and ALL continue to be a major cause of morbidity and mortality worldwide, in part because molecular therapies for the plethora of genetic abnormalities have not been developed. This underscores the current need for better model systems for therapy development. This article reviews the current zebrafish models of AML and ALL and discusses how novel gene editing tools can be implemented to generate better models of acute leukemias. This article is categorized under: Adult Stem Cells, Tissue Renewal, and Regeneration > Stem Cells and Disease Technologies > Perturbing Genes and Generating Modified Animals.

斑马鱼急性白血病模型:当前模型和未来方向。
急性髓性白血病(AML)和急性淋巴性白血病(ALL)是一种异质性疾病,包括一系列具有功能丧失和获得表型的基因突变。最终,这两者都会导致骨髓、外周血和其他组织中成纤维细胞的克隆性过度生长。因此,正常的造血干细胞功能受到严重阻碍。允许早期检测基因改变和了解这些不同分子病理的技术有助于将我们的治疗方案推向个性化的靶向治疗。尽管如此,AML和ALL仍然是全球发病率和死亡率的主要原因,部分原因是尚未开发出针对大量遗传异常的分子疗法。这突出了当前对用于治疗开发的更好的模型系统的需求。本文综述了目前斑马鱼AML和ALL模型,并讨论了如何使用新的基因编辑工具来生成更好的急性白血病模型。这篇文章分类在:成体干细胞,组织更新和再生>干细胞和疾病技术>扰动基因和产生修饰动物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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期刊介绍: Developmental biology is concerned with the fundamental question of how a single cell, the fertilized egg, ultimately produces a complex, fully patterned adult organism. This problem is studied on many different biological levels, from the molecular to the organismal. Developed in association with the Society for Developmental Biology, WIREs Developmental Biology will provide a unique interdisciplinary forum dedicated to fostering excellence in research and education and communicating key advances in this important field. The collaborative and integrative ethos of the WIREs model will facilitate connections to related disciplines such as genetics, systems biology, bioengineering, and psychology. The topical coverage of WIREs Developmental Biology includes: Establishment of Spatial and Temporal Patterns; Gene Expression and Transcriptional Hierarchies; Signaling Pathways; Early Embryonic Development; Invertebrate Organogenesis; Vertebrate Organogenesis; Nervous System Development; Birth Defects; Adult Stem Cells, Tissue Renewal and Regeneration; Cell Types and Issues Specific to Plants; Comparative Development and Evolution; and Technologies.
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