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Global gene expression profiling analysis reveals reduction of stemness after B-RAF inhibition in colorectal cancer cell lines.
Boerries, Melanie; Herr, Ricarda; Brummer, Tilman; Busch, Hauke.
Afiliação
  • Boerries M; Systems Biology of the Cellular Microenvironment Group, Institute of Molecular Medicine and Cell Research (IMMZ), Albert-Ludwigs-University (ALU), Freiburg, Germany ; German Cancer Consortium (DKTK), Freiburg, Germany ; German Cancer Research Center (DKFZ), Heidelberg, Germany.
  • Herr R; Signal Transduction in Tumour Development and Drug Resistance Group, IMMZ, ALU, Freiburg, Germany ; Faculty of Biology, ALU, Freiburg, Germany.
  • Brummer T; Signal Transduction in Tumour Development and Drug Resistance Group, IMMZ, ALU, Freiburg, Germany ; Centre for Biological Signalling Studies BIOSS, ALU, Freiburg, Germany.
  • Busch H; Systems Biology of the Cellular Microenvironment Group, Institute of Molecular Medicine and Cell Research (IMMZ), Albert-Ludwigs-University (ALU), Freiburg, Germany ; German Cancer Consortium (DKTK), Freiburg, Germany ; German Cancer Research Center (DKFZ), Heidelberg, Germany.
Genom Data ; 4: 158-61, 2015 Jun.
Article em En | MEDLINE | ID: mdl-26484206
ABSTRACT
Cancer cell differentiation is an important field of discussion in the light of cancer stem cells. In a recent study by Herr et al. (2015) "B-RAF inhibitors induce epithelial differentiation in BRAF-mutant colorectal cancer cells" we described how inhibition of mutant BRAF in colorectal cancer cell lines induces cell re-differentiation that is correlated with the loss of tumor growth in vitro and in vivo. We used Illumina HumanHT-12 v4 Expression BeadChip to characterize the gain of differentiation of PLX4720-treated 3D cultures of HT29 and Colo-205 cells. Here, we describe the experimental design and statistical analysis that were performed on the data set leading to the above hypothesis. The data are publicly available at the Gene Expression Omnibus (GEO) database under the accession number GSE50791.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2015 Tipo de documento: Article