Genomic analysis of single cells from human basal cell cancer using laser-assisted capture microscopy

Fredrik Pontén , Cecilia Williams , Gao Ling , Afshin Ahmadian , Monica Nistér , Joakim Lundeberg , Jan Pontén , Mathias Uhlén
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引用次数: 50

Abstract

In this study, we show that direct mutational analysis of genomic DNA can be performed on single somatic cells extracted from a frozen, immunohistochemically stained tissue section using laser-assisted capture microscopy. Eighty-nine single tumor cells were separately dissected from one case of human basal cell cancer (BCC) and p53 mutations were analyzed by direct semi-automated sequencing of PCR fragments. Amplification was obtained for at least one of the two analyzed exons from approximately 50% of the single tumor cells. Identical p53 mutations were found in widely spread areas of the tumor, suggesting a clonal proliferation originating from one cell. Interestingly, comparison between results of immunohistochemistry and genetic analysis of the single cells revealed the same p53 mutations irrespective of the p53 immunoreactivity. We propose that this approach has a great potential to allow investigation of genotypic differences in single cells and more specifically to resolve important and fundamental questions determining cancer heterogeneity.

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利用激光辅助捕获显微镜对人类基底细胞癌单细胞进行基因组分析
在这项研究中,我们证明可以使用激光辅助捕获显微镜对从冷冻免疫组织化学染色的组织切片中提取的单个体细胞进行基因组DNA的直接突变分析。本文从1例人基底细胞癌(BCC)中分离89个肿瘤细胞,采用PCR片段直接半自动化测序技术对p53突变进行分析。从大约50%的单个肿瘤细胞中至少获得了两个分析外显子中的一个扩增。在肿瘤的广泛扩散区域发现了相同的p53突变,表明克隆增殖起源于一个细胞。有趣的是,将免疫组化结果与单细胞的遗传分析结果进行比较,发现无论p53免疫反应性如何,p53突变都是相同的。我们提出,这种方法具有很大的潜力,可以研究单细胞的基因型差异,更具体地说,可以解决确定癌症异质性的重要和基本问题。
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VOLUME CONTENTS Comprehensive analysis of a large genomic sequence at the putative B-cell chronic lymphocytic leukaemia (B-CLL) tumour suppresser gene locus Mutational analysis within the 3′ region of the PKD1 gene in Japanese families Allelic polymorphisms in the transcriptional regulatory region of human SEL1L CUMULATIVE AUTHOR INDEX FOR MUTNOM 2000
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