Blixt Maria K E, Hellsand Minas, Konjusha Dardan, Zhang Hanzhao, Stenfelt Sonya, Åkesson Mikael, Rafati Nima, Tararuk Tatsiana, Stålhammar Gustav, All-Eriksson Charlotta, Ring Henrik, Hallböök Finn
Department of Immunology, Genetics, and Pathology, Uppsala University, Uppsala, Sweden.
National Bioinformatics Infrastructure Sweden, Uppsala University, SciLifeLab, Department of Medical Biochemistry and Microbiology, Uppsala, Sweden.
Oncogenesis. 2022 Jun 21;11(1):34. doi: 10.1038/s41389-022-00409-3.
Retinoblastoma is a rare, intraocular paediatric cancer that originates in the neural retina and is most frequently caused by bi-allelic loss of RB1 gene function. Other oncogenic mutations, such as amplification and increased expression of the MYCN gene, have been found even with proficient RB1 function. In this study, we investigated whether MYCN over-expression can drive carcinogenesis independently of RB1 loss-of-function mutations. The aim was to elucidate the events that result in carcinogenesis and identify the cancer cell-of-origin. We used the chicken retina, a well-established model for studying retinal neurogenesis, and established human embryonic stem cell-derived retinal organoids as model systems. We over-expressed MYCN by electroporation of piggyBac genome-integrating expression vectors. We found that over-expression of MYCN induced tumorigenic growth with high frequency in RB1-proficient chicken retinas and human organoids. In both systems, the tumorigenic cells expressed markers for undifferentiated cone photoreceptor/horizontal cell progenitors. The over-expression resulted in metastatic retinoblastoma within 7-9 weeks in chicken. Cells expressing MYCN could be grown in vitro and, when orthotopically injected, formed tumours that infiltrated the sclera and optic nerve and expressed markers for cone progenitors. Investigation of the tumour cell phenotype determined that the potential for neoplastic growth was embryonic stage-dependent and featured a cell-specific resistance to apoptosis in the cone/horizontal cell lineage, but not in ganglion or amacrine cells. We conclude that MYCN over-expression is sufficient to drive tumorigenesis and that a cell-specific resistance to apoptosis in the cone/horizontal cell lineage mediates the cancer phenotype.
视网膜母细胞瘤是一种罕见的儿童眼内癌,起源于神经视网膜,最常见的原因是RB1基因功能的双等位基因缺失。即使RB1功能正常,也发现了其他致癌突变,如MYCN基因的扩增和表达增加。在本研究中,我们调查了MYCN过表达是否能独立于RB1功能丧失突变驱动致癌作用。目的是阐明导致致癌作用的事件并确定癌症起源细胞。我们使用鸡视网膜(一种用于研究视网膜神经发生的成熟模型)和建立的人胚胎干细胞来源的视网膜类器官作为模型系统。我们通过转染piggyBac基因组整合表达载体来过表达MYCN。我们发现,在RB1功能正常的鸡视网膜和人视网膜类器官中,MYCN过表达高频诱导致瘤性生长。在这两个系统中,致瘤细胞均表达未分化的视锥光感受器/水平细胞祖细胞的标志物。过表达在7-9周内导致鸡发生转移性视网膜母细胞瘤。表达MYCN的细胞可以在体外培养,原位注射时会形成浸润巩膜和视神经并表达视锥祖细胞标志物的肿瘤。对肿瘤细胞表型的研究确定,肿瘤生长潜力取决于胚胎阶段,并且在视锥/水平细胞谱系中具有细胞特异性的抗凋亡能力,而在神经节细胞或无长突细胞中则没有。我们得出结论,MYCN过表达足以驱动肿瘤发生,并且视锥/水平细胞谱系中细胞特异性的抗凋亡能力介导了癌症表型。