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将神经母细胞瘤细胞注入实验性成熟畸胎瘤中,发现其对胚胎疏松间充质具有亲嗜性。

Neuroblastoma cells injected into experimental mature teratoma reveal a tropism for embryonic loose mesenchyme.

机构信息

Department of Women's and Children's Health, Karolinska Institute, Stockholm, Sweden.

出版信息

Int J Oncol. 2013 Sep;43(3):831-8. doi: 10.3892/ijo.2013.2014. Epub 2013 Jul 12.

Abstract

Embryonic neural tumors are responsible for a disproportionate number of cancer deaths in children. Although dramatic improvements in survival for pediatric malignancy has been achieved in previous years advancements seem to be slowing down. For the development of new enhanced therapy and an increased understanding of the disease, pre-clinical models better capturing the neoplastic niche are essential. Tumors of early childhood present in this respect a particular challenge. Here, we explore how components of the embryonic process in stem‑cell induced mature teratoma can function as an experimental in vivo microenvironment instigating the growth of injected childhood neuroblastoma (NB) cell lines. Three human NB cell lines, IMR-32, Kelly and SK-N-BE(2), were injected into mature pluripotent stem cell‑induced teratoma (PSCT) and compared to xenografts of the same cell lines. Proliferative NB cells from all lines were readily detected in both models with a typical histology of a poorly differentiated NB tumor with a variable amount of fibrovascular stroma. Uniquely in the PSCT microenvironment, NB cells were found integrated in a non‑random fashion. Neuroblastoma cells were never observed in areas with well-differentiated somatic tissue i.e. bone, muscle, gut or areas of other easily identifiable tissue types. Instead, the three cell lines all showed initial growth exclusively occurring in the embryonic loose mesenchymal stroma, resulting in a histology recapitulating NB native presentation in vivo. Whether this reflects the 'open' nature of loose mesenchyme more easily giving space to new cells compared to other more dense tissues, the rigidity of matrix providing physical cues modulating NB characteristics, or if embryonic loose mesenchyme may supply developmental cues that attracted or promoted the integration of NB, remains to be tested. We tentatively hypothesize that mature PSCT provide an embryonic niche well suited for in vivo studies on NB.

摘要

胚胎神经肿瘤是导致儿童癌症死亡的主要原因。尽管近年来儿科恶性肿瘤的生存率有了显著提高,但进展似乎正在放缓。为了开发新的强化治疗方法并加深对疾病的认识,更好地模拟肿瘤微环境的临床前模型至关重要。在这方面,早期儿童肿瘤尤其具有挑战性。在这里,我们探讨了如何利用诱导成熟畸胎瘤的胚胎过程中的成分作为实验体内微环境,引发注射的儿童神经母细胞瘤(NB)细胞系的生长。将三种人类 NB 细胞系,IMR-32、Kelly 和 SK-N-BE(2),注入成熟多能干细胞诱导的畸胎瘤(PSCT)中,并与相同细胞系的异种移植物进行比较。所有系的增殖性 NB 细胞在这两种模型中均被轻易检测到,具有典型的低分化 NB 肿瘤组织学特征,伴有不同程度的纤维血管基质。在 PSCT 微环境中,NB 细胞以非随机的方式整合。从未在分化良好的体组织(即骨、肌肉、肠道或其他易于识别的组织类型)区域观察到神经母细胞瘤细胞。相反,这三种细胞系的初始生长都仅发生在胚胎疏松的间充质基质中,导致组织学重现了 NB 在体内的固有表现。这是否反映了疏松间充质更容易为新细胞提供空间的“开放性”,而不是其他更密集的组织,基质的刚性提供了调节 NB 特征的物理线索,或者胚胎疏松间充质是否提供了吸引或促进 NB 整合的发育线索,仍有待测试。我们暂拟假设成熟的 PSCT 为 NB 的体内研究提供了一个理想的胚胎微环境。

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