A summary of the work associated to these microarrays is the following:
Coffee polyphenols change the expression of STAT5B and ATF-2 modifying cyclin D1 levels in cancer cells.
Cell line, Treatment
View SamplesThis SuperSeries is composed of the SubSeries listed below.
Networking of differentially expressed genes in human cancer cells resistant to methotrexate.
Specimen part, Cell line
View SamplesA summary of the work associated to these microarrays is the following:
Networking of differentially expressed genes in human cancer cells resistant to methotrexate.
Specimen part, Cell line
View SamplesA summary of the work associated to these microarrays is the following:
Networking of differentially expressed genes in human cancer cells resistant to methotrexate.
Specimen part, Cell line
View SamplesA summary of the work associated to these microarrays is the following:
Networking of differentially expressed genes in human cancer cells resistant to methotrexate.
Specimen part, Cell line
View SamplesA summary of the work associated to these microarrays is the following:
Networking of differentially expressed genes in human cancer cells resistant to methotrexate.
Specimen part, Cell line
View SamplesA summary of the work associated to these microarrays is the following:
Networking of differentially expressed genes in human cancer cells resistant to methotrexate.
Specimen part, Cell line
View SamplesA summary of the work associated to these microarrays is the following:
Networking of differentially expressed genes in human cancer cells resistant to methotrexate.
Specimen part, Cell line
View SamplesSp1 is a transcription factor able to regulate many genes through its DNA binding domain, containing three zinc fingers. We were interested in identifying target genes regulated by Sp1, with a special emphasis to those involved in proliferation and cancer. Our approach was to treat HeLa cells with a siRNA directed against Sp1 mRNA (siSp1) to decrease the expression of Sp1 and, in turn, the genes activated by this transcription factor. Sp1 siRNA treatment led to a great number of differentially expressed genes as determined by whole genome cDNA microarray analysis. Underexpressed genes were selected since they represent putative genes activated by Sp1. These underexpressed genes were classified in six Gene Onthology categories, namely proliferation and cancer, mRNA processing, lipidic metabolism, glucidic metabolism, transcription and translation. Putative Sp1 binding sites were found in the promoters of the selected genes using the MatchTM software. After literature mining, 11 genes were selected for further validation of their expression levels using RT-real time PCR. Underexpression was confirmed for the 11 genes plus Sp1 in HeLa cells after siSp1 treatment. Additionally, EMSA and chromatin immunoprecipitation assays were performed to test for binding between Sp1 and the promoters of these genes. We observed binding of Sp1 to the promoters of RAB20, FGF21, IHPK2, ARHGAP18, NPM3, SRSF7, CALM3, PGD and Sp1 itself. Finally, the mRNA levels of RAB20, FGF21 and IHPK2, three genes related with proliferation and cancer, were determined after overexpression of Sp1 in HeLa cells, to confirm their relationship with Sp1.
Identification of novel Sp1 targets involved in proliferation and cancer by functional genomics.
Specimen part, Cell line
View SamplesThe PR domain containing 1a, with ZNF domain factor, gene prdm1a plays an integral role in the development of a number of different cell types during vertebrate embryogenesis, including neural crest cells, Rohon-Beard (RB) sensory neurons and the cranial neural crest-derived craniofacial skeletal elements. To better understand how Prdm1a regulates the development of various cell types in zebrafish, we performed a microarray analysis comparing wild type and prdm1a mutant embryos and identified a number of genes with altered expression in the absence of prdm1a. Rescue analysis determined that two of these, sox10 and islet1, lie downstream of Prdm1a in the development of neural crest cells and Rohon-Beard neurons, respectively. In addition, we identified a number of other novel downstream targets of Prdm1a that may be important for the development of diverse tissues during zebrafish embryogenesis.
prdm1a Regulates sox10 and islet1 in the development of neural crest and Rohon-Beard sensory neurons.
Age, Specimen part
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