Genome wide in vivo mouse screen data from studies to assess host regulation of metastatic colonisation.

Genome wide in vivo mouse screen data from studies to assess host regulation of metastatic colonisation.
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DOI:
10.1038/sdata.2017.129
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发表时间:
2017-09-12
期刊:
影响因子:
9.8
通讯作者:
Speak AO
Speak AO
中科院分区:
综合性期刊2区
文献类型:
--
作者:
van der Weyden L;Karp NA;Swiatkowska A;Adams DJ;Speak AO

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转移的过程是一个多阶段的级联反应,先前的研究表明继发部位的定殖是限速步骤。这一过程涉及肿瘤细胞以及非肿瘤内在因素如基质和造血系统的作用。在这项研究中,我们目前的数据筛选810转基因小鼠系的实验转移测定,其中静脉内输送的小鼠转移性黑色素瘤B16-F10细胞被用来评估肺转移灶的形成。到目前为止,这些数据已经研究了一个两步的过程中积累的综合数据分析,以确定控制转移定植的基因。我们提供了原始数据和描述,以支持新的分析,研究人员可以在基因组内和跨基因组进行研究,以进一步阐明调节转移性定植的过程。
The process of metastasis is a multi-stage cascade with prior studies suggesting that the colonisation of the secondary site is the rate limiting step. This process involves contributions from the tumour cells and also non-tumour intrinsic factors such as the stroma and the haematopoietic system. In this study, we present data from screening 810 genetically-modified mouse lines with the experimental metastasis assay where intravenous delivery of murine metastatic melanoma B16-F10 cells was used to assess the formation of pulmonary metastasic foci. To date, these data have been studied with a two-step process cumulating in an integrative data analysis to identify genes controlling metastatic colonisation. We present the raw data, and a description to support fresh analyses where researchers can look both within and across gene sets to further elucidate process that regulate metastatic colonisation.
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