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Home › Dataset Library › Transcription profiling of human skeletal muscle of PCOS patients after pioglitazone therapy

Dataset: Transcription profiling of human skeletal muscle of PCOS patients after pioglitazone therapy

Insulin resistance is a common metabolic abnormality in women with PCOS and leads to an elevated risk of type 2 diabetes. Studies have...

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Insulin resistance is a common metabolic abnormality in women with PCOS and leads to an elevated risk of type 2 diabetes. Studies have shown that thiazolidinediones (TZD) improve metabolic disturbances in PCOS patients. We hypothesized that the effect of TZD in PCOS is in part mediated by changes in the transcriptional profile of muscle favoring insulin sensitivity. Using Affymetrix microarrays, we examined the effect of pioglitazone (30 mg/day for 16 weeks) on gene expression in skeletal muscle of 10 obese women with PCOS metabolically characterized by a euglycemic-hyperinsulinemic clamp. Moreover, we explored gene expression changes between these PCOS patients before treatment and 13 healthy control women. Treatment with pioglitazone improved insulin-stimulated total, oxidative and non-oxidative glucose metabolism, and reduced fasting serum insulin (all p < 0.05). Global pathway analysis using Gene Map Annotator and Pathway Profiler (GenMAPP 2.1) and Gene Set Enrichment Analysis (GSEA 2.0.1) revealed a significant upregulation of genes involved in mitochondrial oxidative phosphorylation (OXPHOS), ribosomal proteins, mRNA processing reactome, translation factors, and proteasome complexes in PCOS patients after pioglitazone therapy. Quantitative real-time PCR suggested that upregulation of OXPHOS genes was mediated by an increase in PGC-1α expression (p < 0.05). Expression of genes involved in ribosomal proteins and OXPHOS was down-regulated in PCOS patients before treatment compared to matched healthy women using GenMAPP 2.1 and GSEA 2.1. These data indicate that pioglitazone therapy restores insulin sensitivity in part by a coordinated upregulation of genes involved in mitochondrial oxidative metabolism and protein biosynthesis in skeletal muscle of PCOS. These transcriptional effects of pioglitazone therapy may contribute to prevent the onset of type 2 diabetes in these women. Experiment Overall Design: Ten obese women of reproductive age with PCOS participated in the study to test the effect of pioglitazone therapy (data set 1). To test if pioglitazone ameliorate existing defects in PCOS patients, the expression profile of the 10 PCOS patients before treatment were compared to the same cohort of 13 control subjects (data set 2).

Species:
human

Samples:
43

Source:
E-GEOD-8157

PubMed:
18560589

Updated:
Dec.12, 2014

Registered:
Sep.22, 2014


Factors: (via ArrayExpress)
Sample
GSE8157GSM201542
GSE8157GSM201543
GSE8157GSM201544
GSE8157GSM201545
GSE8157GSM201829
GSE8157GSM201830
GSE8157GSM201831
GSE8157GSM201832
GSE8157GSM201833
GSE8157GSM201834
GSE8157GSM201835
GSE8157GSM201836
GSE8157GSM201837
GSE8157GSM201838
GSE8157GSM201839
GSE8157GSM201840
GSE8157GSM201841
GSE8157GSM201842
GSE8157GSM201843
GSE8157GSM201844
GSE8157GSM201849
GSE8157GSM201850
GSE8157GSM201851
GSE8157GSM201852
GSE8157GSM201853
GSE8157GSM201854
GSE8157GSM201855
GSE8157GSM201856
GSE8157GSM201857
GSE8157GSM201858
GSE8157GSM201859
GSE8157GSM201861
GSE8157GSM201862
GSE8157GSM201863
GSE8157GSM201864
GSE8157GSM201865
GSE8157GSM201866
GSE8157GSM201867
GSE8157GSM201868
GSE8157GSM201869
GSE8157GSM201870
GSE8157GSM201871
GSE8157GSM201872

Tags

  • glucose
  • insulin
  • muscle
  • pcos
  • protein
  • serum

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