1] INSERM, UMR 957, Equipe Labellisée LIGUE 2012, Nantes, France [2] Université de Nantes, Nantes Atlantique Universités, Laboratoire de Physiopathologie de la Résorption Osseuse et Thérapie des Tumeurs Osseuses Primitives, Nantes, France [3] Atlantic Bone Screen (ABS), St Herblain, France.
Lab Invest. 2013 Oct;93(10):1100-14. doi: 10.1038/labinvest.2013.101. Epub 2013 Aug 19.
Chondrosarcomas are cartilage-forming, poorly vascularized tumors. They represent the second malignant primary bone tumor of adults after osteosarcoma, but in contrast to osteosarcoma they are resistant to chemotherapy and radiotherapy, surgical excision remaining the only therapeutic option. Few cell lines and animal models are available, and the mechanisms behind their chemoresistance remain largely unknown. Our goal was to establish new cell lines and animal cancer models from human chondrosarcoma biopsies to study their chemoresistance. Between 2007 and 2012, 10 chondrosarcoma biopsies were collected and used for cell culture and transplantation into nude mice. Only one transplanted biopsy and one injected cell line has engrafted successfully leading to conventional central high-grade chondrosarcoma similar to the original biopsies. In culture, two new stable cell lines were obtained, one from a dedifferentiated and one from a grade III conventional central chondrosarcoma biopsy. Their genetic characterization revealed triploid karyotypes, mutations in IDH1, IDH2, and TP53, deletion in CDKN2A and/or MDM2 amplification. These cell lines expressed mesenchymal membrane markers (CD44, 73, 90, 105) and were able to produce a hyaline cartilaginous matrix when cultured in chondrogenic three-dimensional (3D) pellets. Using a high-throughput quantitative RT-PCR approach, we observed that cell lines cultured in monolayer had lost expression of several genes implicated in cartilage development (COL2A1, COMP, ACAN) but restored their expression in 3D cultures. Chondrosarcoma cells in monolayer were sensitive to several conventional chemotherapeutic agents but became resistant to low doses of mafosfamide or doxorubicin when cultured in 3D pellets, in parallel with an altered nucleic accumulation of the drug. Our results indicate that the cartilaginous matrix produced by chondrosarcoma cells may impair diffusion of several drugs and thus contribute to chemoresistance. Therefore, 3D chondrogenic cell pellets constitute a more relevant model to study chondrosarcoma chemoresistance and may be a valuable alternative to animal experimentations.
软骨肉瘤是一种形成软骨的、血供不良的肿瘤。它是继骨肉瘤之后成年人的第二大恶性原发性骨肿瘤,但与骨肉瘤不同的是,它对化疗和放疗具有抗性,手术切除仍然是唯一的治疗选择。目前可用的细胞系和动物模型很少,其化疗抗性的机制在很大程度上仍不清楚。我们的目标是从人类软骨肉瘤活检中建立新的细胞系和动物癌症模型,以研究它们的化疗抗性。在 2007 年至 2012 年期间,收集了 10 例软骨肉瘤活检进行细胞培养和移植到裸鼠中。只有一个移植的活检和一个注射的细胞系成功植入,导致与原始活检相似的常规中央高级别软骨肉瘤。在培养中,获得了两个新的稳定细胞系,一个来自去分化的,一个来自 III 级常规中央软骨肉瘤活检。它们的遗传特征显示三倍体核型、IDH1、IDH2 和 TP53 的突变、CDKN2A 的缺失和/或 MDM2 的扩增。这些细胞系表达间充质膜标志物(CD44、73、90、105),并在三维(3D)球状体培养时能够产生透明软骨基质。使用高通量定量 RT-PCR 方法,我们观察到在单层培养的细胞系中,一些参与软骨发育的基因(COL2A1、COMP、ACAN)的表达丢失,但在 3D 培养中恢复了其表达。在单层培养的软骨肉瘤细胞对几种常规化疗药物敏感,但当在 3D 球状体中培养时,对低剂量的甲氨蝶呤或阿霉素产生耐药性,同时药物的核酸积累也发生改变。我们的结果表明,软骨肉瘤细胞产生的软骨基质可能会阻碍几种药物的扩散,从而导致化疗抗性。因此,3D 软骨生成细胞球状体构成了研究软骨肉瘤化疗抗性的更相关模型,并且可能是动物实验的有价值替代品。