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MYC, TP53, and Chromosome 17 Copy-Number Alterations in Multiple Gastric Cancer Cell Lines and in Their Parental Primary Tumors

机译:MYC,TP53和染色体17拷贝数变化在多个胃癌细胞系及其父母原发性肿瘤中

摘要

We evaluated whether MYC, TP53, and chromosome 17 copy-number alterations occur in ACP02, ACP03, and AGP01 gastric cancer cell lines and in their tumor counterpart. Fluorescence in situ hybridization for MYC and TP53 genes and for chromosome 17 was applied in the 6th, 12th, 60th, and 85th passages of the cell lines and in their parental primary tumors. We observed that three and four MYC signals were the most common alterations in gastric cell lines and tumors. ACP02 presented cells with two copies of chr17 and loss of one copy of TP53 more frequently than ACP03 and AGP01. Only ACP03 and AGP01 presented clonal chr17 trisomy with three or two TP53 copies. the frequency of MYC gain, TP53 loss, and chromosome 17 trisomy seems to increase in gastric cell lines compared to their parental tumors. Our findings reveal that these cell lines retain, in vitro, the genetic alterations presented in their parental primary tumors.
机译:我们评估了MYC,TP53和17号染色​​体的拷贝数变化是否发生在ACP02,ACP03和AGP01胃癌细胞系以及它们的肿瘤对应物中。 MYC和TP53基因以及17号染色​​体的荧光原位杂交应用于细胞系的第6、12、60和85代及其亲代原发性肿瘤。我们观察到三个和四个MYC信号是胃细胞系和肿瘤中最常见的改变。与ACP03和AGP01相比,ACP02为细胞提供了两个拷贝的chr17拷贝和一个拷贝的TP53丢失。只有ACP03和AGP01呈现了克隆的chr17三体性,带有三个或两个TP53拷贝。与亲本肿瘤相比,胃细胞系中MYC增益,TP53缺失和17号染色​​体三体性的频率似乎增加。我们的发现表明,这些细胞系在体外保留了其亲代原发肿瘤中的遗传改变。

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