This dataset contains processed transcriptomic and proteomic data generated from inguinal white adipose tissue collected from control mice, obesity-associated PCOS model mice, and PCOS mice treated with high-dose Atractylodis Rhizoma-derived exosome-like nanovesicles (AR-ELNs). These data support the multi-omics analyses presented in the associated manuscript and were used to characterize adipose metabolic-endocrine remodeling, with particular focus on kynurenine pathway activation and AhR/AR-related gene and protein programs in obesity-associated PCOS. The dataset includes processed RNA-seq differential expression tables and quantitative proteomics differential expression tables for the following comparisons: PCOS_vs_CTRL_iWAT_RNAseq_DEG_all_genes.xlsx Gene-level differential expression results comparing inguinal white adipose tissue from obesity-associated PCOS model mice with control mice. PCOS_H-ELNs_vs_PCOS_iWAT_RNAseq_DEG_all_genes.xlsx Gene-level differential expression results comparing inguinal white adipose tissue from PCOS mice treated with high-dose AR-ELNs with untreated PCOS model mice. PCOS_vs_CTRL_iWAT_Proteomics_DEP_all_proteins.xlsx Protein-level differential expression results comparing inguinal white adipose tissue from obesity-associated PCOS model mice with control mice. PCOS_H-ELNs_vs_PCOS_iWAT_Proteomics_DEP_all_proteins.xlsx Protein-level differential expression results comparing inguinal white adipose tissue from PCOS mice treated with high-dose AR-ELNs with untreated PCOS model mice. These processed datasets include gene- or protein-level identifiers, expression or abundance changes, fold-change values, statistical significance values, and annotation fields used for downstream pathway enrichment, integrated transcriptomic-proteomic analysis, and candidate pathway selection. The data are provided to support transparency and reproducibility of the multi-omics analyses reported in the manuscript.
This dataset contains processed transcriptomic and proteomic data generated from inguinal white adipose tissue collected from control mice, obesity-associated PCOS model mice, and PCOS mice treated with high-dose Atractylodis Rhizoma-derived exosome-like nanovesicles (AR-ELNs). These data support the multi-omics analyses presented in the associated manuscript and were used to characterize adipose metabolic-endocrine remodeling, with particular focus on kynurenine pathway activation and AhR/AR-related gene and protein programs in obesity-associated PCOS. The dataset includes processed RNA-seq differential expression tables and quantitative proteomics differential expression tables for the following comparisons: PCOS_vs_CTRL_iWAT_RNAseq_DEG_all_genes.xlsx Gene-level differential expression results comparing inguinal white adipose tissue from obesity-associated PCOS model mice with control mice. PCOS_H-ELNs_vs_PCOS_iWAT_RNAseq_DEG_all_genes.xlsx Gene-level differential expression results comparing inguinal white adipose tissue from PCOS mice treated with high-dose AR-ELNs with untreated PCOS model mice. PCOS_vs_CTRL_iWAT_Proteomics_DEP_all_proteins.xlsx Protein-level differential expression results comparing inguinal white adipose tissue from obesity-associated PCOS model mice with control mice. PCOS_H-ELNs_vs_PCOS_iWAT_Proteomics_DEP_all_proteins.xlsx Protein-level differential expression results comparing inguinal white adipose tissue from PCOS mice treated with high-dose AR-ELNs with untreated PCOS model mice. These processed datasets include gene- or protein-level identifiers, expression or abundance changes, fold-change values, statistical significance values, and annotation fields used for downstream pathway enrichment, integrated transcriptomic-proteomic analysis, and candidate pathway selection. The data are provided to support transparency and reproducibility of the multi-omics analyses reported in the manuscript.
Linxia Li· Mendeley Data· 0 citations
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