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Identification of alterations in DNA copy number in host stromal cells during tumor progression

机译:鉴定肿瘤进展过程中宿主基质细胞DNA拷贝数的变化

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The interactions between cancer cells and the surrounding host stromal tissue play a critical role in tumor progression and metastasis, but the molecular nature of this relationship remains largely uncharacterized. Furthermore, although genetic changes of neo-plastic cells in tumors contribute significantly to tumor progression, it is not known whether similar changes occur in the adjacent host stromal microenvironment and whether they contribute to or inhibit tumorigenesis. To address this question in an unbiased and genome-wide manner, we applied high-resolution DNA copy number analysis to murine stromal DNA isolated from human xenograft tumors that were formed in immunodeficient mice. We show that numerous amplifications and deletions are found within the host stromal microenvironment, suggesting that alterations in host DNA copy number can occur and may play a significant role in modifying tumor-stromal interactions.
机译:癌细胞与周围宿主基质组织之间的相互作用在肿瘤的进展和转移中起着至关重要的作用,但是这种关系的分子性质在很大程度上仍未表征。此外,尽管肿瘤中赘生性细胞的遗传变化显着地促进了肿瘤的进展,但尚不清楚相邻宿主基质微环境中是否发生类似的变化,以及它们是否有助于或抑制肿瘤发生。为了以无偏见和全基因组的方式解决这个问题,我们将高分辨率的DNA拷贝数分析应用于从免疫缺陷小鼠中形成的人异种移植肿瘤分离的鼠基质DNA。我们表明,在宿主基质微环境中发现了许多扩增和缺失,表明宿主DNA拷贝数的改变可能发生,并且可能在修饰肿瘤-基质相互作用中起重要作用。

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