Samples were taken from colorectal cancers in surgically resected specimens in 35 colorectal cancer patients. The expression profiles were determined using Affymetrix Human Genome U133 Plus 2.0 arrays. Comparison between the sample groups allow to identify a set of discriminating genes that can be used for molecular markers for CIN phynotype.
Chromosomal instability (CIN) phenotype, CIN high or CIN low, predicts survival for colorectal cancer.
Specimen part
View SamplesSamples were taken from colorectal cancers in surgically resected specimens in 33 colorectal cancer patients. The expression profiles were determined using Affymetrix Human Genome U133 Plus 2.0 arrays. Comparison between the sample groups allow to identify a set of discriminating genes that can be used for molecular markers for CIN phynotype
Chromosomal instability (CIN) phenotype, CIN high or CIN low, predicts survival for colorectal cancer.
Specimen part
View SamplesThe objective of this study is to search for calcium signal-dependent expression changes.
Calcium-dependent N-cadherin up-regulation mediates reactive astrogliosis and neuroprotection after brain injury.
Specimen part
View SamplesThis SuperSeries is composed of the SubSeries listed below.
PU.1 is a potent tumor suppressor in classical Hodgkin lymphoma cells.
Cell line, Time
View SamplesPU.1 is an Ets family transcription factor that is essential for the differentiation of both myeloid and lymphoid cells. PU.1 is down-regulated in classical Hodgkin lymphoma cells via methylation of the PU.1 promoter. To evaluate whether down-regulation of PU.1 is essential for the growth of cHL cells, we generated KM-H2 derived cell lines conditionally express PU.1 by tet-off system (designated KM-H2tetPU.1). Conditonally expressed PU.1 by tetracycline removal induced complete growth arrest and apoptosis in KM-H2 cells. To elucidate the mechanisms underlying cell cycle arrest and apoptosis induced by PU.1, we compared gene expression profiles of KM-H2tetPU.1 cells 0, 1 and 3 days after PU.1 induction, by DNA microarray.
PU.1 is a potent tumor suppressor in classical Hodgkin lymphoma cells.
Cell line, Time
View Samples