Cao Dongliang, Kishida Satoshi, Huang Peng, Mu Ping, Tsubota Shoma, Mizuno Masaaki, Kadomatsu Kenji
Department of Biochemistry, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Center for Advanced Medicine and Clinical Research, Nagoya University Hospital. Nagoya, Japan.
PLoS One. 2014 Jan 22;9(1):e86813. doi: 10.1371/journal.pone.0086813. eCollection 2014.
Tumorsphere culture enriches and expands tumor cells, thus providing important resources for cancer studies. However, as compared with metastatic tissues, primary tumors in the nervous system rarely give rise to long-surviving tumorspheres, thereby seriously limiting studies on these cancers. This might be due to the limited self-renewal capability of tumor cells and/or to inappropriate culture conditions. The growth and maintenance of tumor cells may depend on microenvironments and/or cell origins (e.g., primary or metastatic; stem cell-like or progenitor-like). Here, we attempted to establish a tumorsphere culture condition for primary neuroblastoma (NB). Primary tumors in MYCN transgenic mice, a NB model, could be serially transplanted, suggesting that these tumors contain cells with a high self-renewal potential. However, primary tumors did not give rise to tumorspheres under a serum-free neurosphere culture condition. The newly established culture condition (named PrimNeuS) contained two critical ingredients: fetal bovine serum and β-mercaptoethanol were essential for tumorsphere formation as well as indefinite passages. The spheres could be passaged more than 20 times without exhaustion under this condition, exhibited a property of differentiation and formed tumors in vivo. Unexpectedly, PrimNeuS revealed that the MYCN transgenic mice had bone marrow metastasis. Furthermore, subcutaneous tumors derived from tumorspheres of primary tumors showed bone marrow metastasis. Taken together, PrimNeuS provides resources for the study of NB and can be used as a powerful tool for the detection of minimal residual disease and for in vitro evaluation prior to personalized therapy.
肿瘤球培养可富集和扩增肿瘤细胞,从而为癌症研究提供重要资源。然而,与转移组织相比,神经系统中的原发性肿瘤很少能产生长期存活的肿瘤球,这严重限制了对这些癌症的研究。这可能是由于肿瘤细胞的自我更新能力有限和/或培养条件不合适。肿瘤细胞的生长和维持可能取决于微环境和/或细胞来源(例如,原发性或转移性;干细胞样或祖细胞样)。在此,我们试图为原发性神经母细胞瘤(NB)建立一种肿瘤球培养条件。NB模型MYCN转基因小鼠中的原发性肿瘤可以连续传代移植,这表明这些肿瘤含有具有高自我更新潜力的细胞。然而,在无血清神经球培养条件下,原发性肿瘤并未产生肿瘤球。新建立的培养条件(命名为PrimNeuS)包含两个关键成分:胎牛血清和β-巯基乙醇对于肿瘤球形成以及无限传代至关重要。在此条件下,球体可以传代20多次而不耗尽,表现出分化特性并在体内形成肿瘤。出乎意料的是,PrimNeuS显示MYCN转基因小鼠发生了骨髓转移。此外,源自原发性肿瘤肿瘤球的皮下肿瘤也显示出骨髓转移。综上所述,PrimNeuS为NB研究提供了资源,可作为检测微小残留病和个性化治疗前体外评估的有力工具。