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Additional file 4: of Expression profiling of in vivo ductal carcinoma in situ progression models identified B cell lymphoma-9 as a molecular driver of breast cancer invasion

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https://springernature.figshare.com/articles/dataset/Additional_file_4_of_Expression_profiling_of_in_vivo_ductal_carcinoma_in_situ_progression_models_identified_B_cell_lymphoma-9_as_a_molecular_driver_of_breast_cancer_invasion/4445363
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Wnt-pathway-specific genes differentially expressed in ductal carcinoma in situ DCIS.COM and SUM225 mouse intraductal xenograft model (MIND) xenografts during transition from 2 to 6 weeks. Genes significantly differentially expressed between the 2- to 6-week time point in both DCIS.COM and SUM225 cell lines were further analyzed using Ingenuity Pathway AnalysisŽ (IPA). The Wnt/β-catenin canonical pathway was identified as a significantly upregulated pathway in both cell line MIND xenografts during transition from 2 to 6 weeks. (XLS 48 kb)

在2周至6周的过渡阶段中,于导管原位癌(ductal carcinoma in situ, DCIS)细胞系DCIS.COM与SUM225小鼠导管内移植瘤模型(mouse intraductal xenograft model, MIND)移植瘤内差异表达的Wnt通路特异性基因。针对DCIS.COM与SUM225两种细胞系在2周龄与6周龄时间点间存在显著差异表达的基因,采用英格诺斯通路分析(Ingenuity Pathway Analysis, IPA)开展进一步分析。在2周至6周的过渡阶段中,Wnt/β-连环蛋白经典通路被证实为两种细胞系来源的MIND移植瘤中显著上调的通路。(XLS 48 kb)
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Figshare
创建时间:
2016-12-15
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