Transcriptome profiling in response to adiponectin in human cancer-derived cells

被引:9
作者
Berger, Emmanuelle [1 ]
Rome, Sophie
Vega, Nathalie
Ciancia, Claire
Vidal, Hubert
机构
[1] Univ Lyon, Hosp Civils Lyon, INSERM, INRA,U870,U1235, F-69008 Lyon, France
关键词
human cancer cell line; microarray; signal transduction; transcription factor; serine/threonine kinase 11; 5 '-adenosine monophosphate-activated protein kinase; hairy and enhancer of split 1; ACTIVATED PROTEIN-KINASE; FATTY-ACID OXIDATION; CIRCULATING ADIPONECTIN; PLASMA ADIPONECTIN; PROSTATE-CANCER; SKELETAL-MUSCLE; GLOBULAR ADIPONECTIN; MICROARRAY ANALYSES; ENDOMETRIAL CANCER; GENE-EXPRESSION;
D O I
10.1152/physiolgenomics.00013.2010
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Berger E, Rome S, Vega N, Ciancia C, Vidal H. Transcriptome profiling in response to adiponectin in human cancer-derived cells. Physiol Genomics 42A: 61-70, 2010. First published June 22, 2010; doi:10.1152/physiolgenomics.00013.2010.-The adipocyte-derived hormone adiponectin exerts protective actions in several disorders, including some cancers. However, while growing data suggest that adiponectin could be an effective anticancer agent, its mechanism of action in cancer cells is still poorly known. Here, using microarrays, we identified a set of 1,301 genes commonly modulated in three cancer-derived cell lines in response to short-term stimulation with full-length recombinant human adiponectin. Most of these genes are involved in translation regulation, immune or stress responses, and cell proliferation. Furthermore, among genes linked to disease that were retrieved by functional enrichment tests using text mining based on PubMed analysis, we found that 66% are involved in malignant neoplasms, further supporting the link between adiponectin and cancer mechanisms. Bioinformatic analysis demonstrated the diversity of signaling pathways and transcription factors potentially mediating adiponectin effects on gene expression, illustrating the complexity of adiponectin mechanisms of action in cancer cells.
引用
收藏
页码:61 / 70
页数:10
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