Kobar Kim, Collett Keon, Prykhozhij Sergey V, Berman Jason N
Children's Hospital of Eastern Ontario Research Institute, Ottawa, ON, Canada.
Department of Cellular and Molecular Medicine, University of Ottawa, Ottawa, ON, Canada.
Front Cell Dev Biol. 2021 Apr 27;9:660069. doi: 10.3389/fcell.2021.660069. eCollection 2021.
Cancer predisposition syndromes are rare, typically monogenic disorders that result from germline mutations that increase the likelihood of developing cancer. Although these disorders are individually rare, resulting cancers collectively represent 5-10% of all malignancies. In addition to a greater incidence of cancer, affected individuals have an earlier tumor onset and are frequently subjected to long-term multi-modal cancer screening protocols for earlier detection and initiation of treatment. models are needed to better understand tumor-driving mechanisms, tailor patient screening approaches and develop targeted therapies to improve patient care and disease prognosis. The zebrafish () has emerged as a robust model for cancer research due to its high fecundity, time- and cost-efficient genetic manipulation and real-time high-resolution imaging. Tumors developing in zebrafish cancer models are histologically and molecularly similar to their human counterparts, confirming the validity of these models. The zebrafish platform supports both large-scale random mutagenesis screens to identify potential candidate/modifier genes and recently optimized genome editing strategies. These techniques have greatly increased our ability to investigate the impact of certain mutations and how these lesions impact tumorigenesis and disease phenotype. These unique characteristics position the zebrafish as a powerful tool to model cancer predisposition syndromes and as such, several have already been created, including those recapitulating Li-Fraumeni syndrome, familial adenomatous polyposis, RASopathies, inherited bone marrow failure syndromes, and several other pathogenic mutations in cancer predisposition genes. In addition, the zebrafish platform supports medium- to high-throughput preclinical drug screening to identify compounds that may represent novel treatment paradigms or even prevent cancer evolution. This review will highlight and synthesize the findings from zebrafish cancer predisposition models created to date. We will discuss emerging trends in how these zebrafish cancer models can improve our understanding of the genetic mechanisms driving cancer predisposition and their potential to discover therapeutic and/or preventative compounds that change the natural history of disease for these vulnerable children, youth and adults.
癌症易感性综合征是罕见的、典型的单基因疾病,由种系突变引起,这些突变会增加患癌的可能性。尽管这些疾病个体发病率较低,但由此导致的癌症合计占所有恶性肿瘤的5%至10%。除了癌症发病率更高外,受影响个体的肿瘤发病更早,并且经常接受长期的多模式癌症筛查方案,以便更早地发现和开始治疗。需要建立模型来更好地理解肿瘤驱动机制、定制患者筛查方法并开发靶向治疗,以改善患者护理和疾病预后。由于斑马鱼繁殖力高、基因操作具有时间和成本效益以及可进行实时高分辨率成像,它已成为癌症研究的强大模型。斑马鱼癌症模型中发生的肿瘤在组织学和分子水平上与其人类对应物相似,证实了这些模型的有效性。斑马鱼平台既支持大规模随机诱变筛选以识别潜在的候选/修饰基因,也支持最近优化的基因组编辑策略。这些技术极大地提高了我们研究某些突变的影响以及这些损伤如何影响肿瘤发生和疾病表型的能力。这些独特的特性使斑马鱼成为模拟癌症易感性综合征的强大工具,因此,已经创建了几种模型,包括那些重现李-弗劳梅尼综合征、家族性腺瘤性息肉病、RAS病、遗传性骨髓衰竭综合征以及癌症易感基因中的其他几种致病突变的模型。此外,斑马鱼平台支持中高通量临床前药物筛选,以识别可能代表新治疗模式甚至预防癌症进展的化合物。本综述将重点介绍并综合迄今为止创建的斑马鱼癌症易感性模型的研究结果。我们将讨论这些斑马鱼癌症模型在如何提高我们对驱动癌症易感性的遗传机制的理解以及它们发现改变这些易患疾病的儿童、青年和成人疾病自然史的治疗和/或预防化合物的潜力方面的新趋势。