Department of Pathology, Leiden University Medical Center, Albinusdreef 2, 2333, ZA, Leiden, The Netherlands.
BMC Cancer. 2012 Aug 28;12:375. doi: 10.1186/1471-2407-12-375.
Chondrosarcoma is the second most common primary sarcoma of bone. High-grade conventional chondrosarcoma and dedifferentiated chondrosarcoma have a poor outcome. In pre-clinical research aiming at the identification of novel treatment targets, the need for representative cell lines and model systems is high, but availability is scarce.
We developed and characterized three cell lines, derived from conventional grade III chondrosarcoma (L835), and dedifferentiated chondrosarcoma (L2975 and L3252) of bone. Proliferation and migration were studied and we used COBRA-FISH and array-CGH for karyotyping and genotyping. Immunohistochemistry for p16 and p53 was performed as well as TP53 and IDH mutation analysis. Cells were injected into nude mice to establish their tumorigenic potential.
We show that the three cell lines have distinct migrative properties, L2975 had the highest migration rate and showed tumorigenic potential in mice. All cell lines showed chromosomal rearrangements with complex karyotypes and genotypic aberrations were conserved throughout late passaging of the cell lines. All cell lines showed loss of CDKN2A, while TP53 was wild type for exons 5-8. L835 has an IDH1 R132C mutation, L2975 an IDH2 R172W mutation and L3252 is IDH wild type.
Based on the stable culturing properties of these cell lines and their genotypic profile resembling the original tumors, these cell lines should provide useful functional models to further characterize chondrosarcoma and to evaluate new treatment strategies.
软骨肉瘤是骨的第二大常见原发性肉瘤。高级别常规软骨肉瘤和去分化软骨肉瘤的预后较差。在旨在确定新的治疗靶点的临床前研究中,对代表性细胞系和模型系统的需求很高,但可用性却很少。
我们开发并鉴定了三个细胞系,源自骨的常规 III 级软骨肉瘤(L835)和去分化软骨肉瘤(L2975 和 L3252)。研究了增殖和迁移,并使用 COBRA-FISH 和 array-CGH 进行核型分析和基因分型。进行了 p16 和 p53 的免疫组织化学染色,并进行了 TP53 和 IDH 突变分析。将细胞注射到裸鼠中以建立其致瘤潜力。
我们表明,这三个细胞系具有不同的迁移特性,L2975 的迁移率最高,并在小鼠中显示出致瘤潜力。所有细胞系均显示染色体重排,具有复杂的核型,并且在细胞系的后期传代过程中保持了基因异常。所有细胞系均显示 CDKN2A 缺失,而 TP53 的外显子 5-8 为野生型。L835 具有 IDH1 R132C 突变,L2975 具有 IDH2 R172W 突变,L3252 为 IDH 野生型。
基于这些细胞系的稳定培养特性及其与原始肿瘤相似的基因谱,这些细胞系应提供有用的功能模型,以进一步表征软骨肉瘤并评估新的治疗策略。