rma-normalized mrna expression data (GeneCentric Diagnostics)
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Rma Normalized Mrna Expression Data, supplied by GeneCentric Diagnostics, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Article Title: Transcriptome- and proteome-oriented identification of dysregulated eIF4G, STAT3, and Hippo pathways altered by PIK3CA H1047R in HER2/ER-positive breast cancer
Journal: Breast cancer research and treatment
doi: 10.1007/s10549-016-4011-9
Figure Legend Snippet: Box plots showing the representative differential proteins in ER+PIK3CAH1047R versus ER+PIK3CAWT subgroups. a The top 5 upregulated and down-regulated proteins or phosphoproteins (y-axis by protein expression) in ER+PIK3CAH1047R patients versus ER+ PIK3CAWT subgroup, respectively. b Box plot view showing the ratio of phosphoprotein to total protein level for 2 representative proteins (AKT and YAP), phosphoprotein (STAT3) and protein (BCL-XL) differential expression, and mRNA differential expression for YAP1 and two YAP1 target genes (TEAD1 and CTGF) altered by PIK3CAH1047R in ER+ breast cancer. The phosphorylation sites in phosphoprotein were labeled by subscript text. The P values were calculated by Wilcoxon rank-sum test for protein differential expression analysis and by edgeR software for mRNA differential expression analysis. The detailed data are provided in Supplementary Table 3
Techniques Used: Expressing, Quantitative Proteomics, Phospho-proteomics, Labeling, Software
Figure Legend Snippet: A gene co-expression-weighted protein interaction subnetwork for YAP1 and the relationship between mRNA expression and drug responses in breast cancer cell lines based on the GDSC dataset [55]. a A gene co-expression-weighted protein interaction subnetwork connecting YAP1 and its 58 interacting proteins. The red edges denote positive co-expression and blue edges denote negative co-expression. The different color keys on nodes represent significance (P values) of gene co-expression measured by F statistics. Gene co-expression analysis was performed based on ER+PIK3CAH1047R breast invasive carcinoma dataset (RNA-seq with V2 RSEM) from TCGA. b Heat map showing the Pearson correlation coefficient (color key) between drug responses and gene mRNA expression for YAP1 and its 58 interacting genes based on the GDSC dataset [55] including 130 drugs’ response data (IC50, the natural log micromolar) and microarray expression across 53 breast cancer cell lines. The labels at the right side are genes and in the bottom are drugs. YAP1 and its two important target genes (TEAD1 and CTGF) were highlighted by red. c Four significant correlation (r: Pearson correlation coefficient) pairs between YAP1 mRNA expression and drug resistance. The P values were performed by F statistics
Techniques Used: Expressing, RNA Sequencing, Microarray
Figure Legend Snippet: Relationship between YAP1 mRNA expression and drug responses in breast cancer cell lines based on the SU2C dataset [26]. a Heat map showing the Pearson correlation coefficient (color key) between drug responses and gene expression for YAP1 and its 58 interacting genes based on the SU2C dataset [26] containing 73 drugs’ response data (−log10(GI50)) and microarray expression across 45 breast cancer cell lines. The labels at the right side are genes and in the bottom are drugs. b Three significant correlation (r: Pearson correlation coefficient) pairs between YAP1 mRNA expression and drug sensitivity. The P values were performed by F statistics
Techniques Used: Expressing, Gene Expression, Microarray
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Furthermore, PIK3CA mutations are commonly associated with resistance to anti-epidermal growth factor receptor 2 (HER2) or anti-estrogen receptor (ER) agents in HER2 or ER positive (HER2/ER) breast cancer.. Hence, deciphering the underlying mechanisms of PIK3CA mutations in HER2/ER breast cancer would provide novel insights into elucidating resistance to anti-HER2/ER therapies. Article Title: Transcriptome- and proteome-oriented identification of dysregulated eIF4G, STAT3, and Hippo pathways altered by PIK3CA H1047R in HER2/ER-positive breast cancer Article Snippet: We also collected microarray gene expression data for breast cancer cell lines from two sources: (i) Article Title: Sister chromatid cohesion defects are associated with chromosome instability in Hodgkin lymphoma cells Article Snippet: All data is extracted from the Labeling:Article Title: Transcriptome- and proteome-oriented identification of dysregulated eIF4G, STAT3, and Hippo pathways altered by PIK3CA H1047R in HER2/ER-positive breast cancer. Article Snippet: Purpose Phosphatidylinositol 3-kinase (PI3K)/AKT pathway aberrations are common in human breast cancer.. Furthermore, PIK3CA mutations are commonly associated with resistance to anti-epidermal growth factor receptor 2 (HER2) or anti-estrogen receptor (ER) agents in HER2 or ER positive (HER2/ER) breast cancer.. Hence, deciphering the underlying mechanisms of PIK3CA mutations in HER2/ER breast cancer would provide novel insights into elucidating resistance to anti-HER2/ER therapies. Article Title: Transcriptome- and proteome-oriented identification of dysregulated eIF4G, STAT3, and Hippo pathways altered by PIK3CA H1047R in HER2/ER-positive breast cancer Article Snippet: We also collected microarray gene expression data for breast cancer cell lines from two sources: (i) Article Title: Sister chromatid cohesion defects are associated with chromosome instability in Hodgkin lymphoma cells Article Snippet: All data is extracted from the Software:Article Title: Transcriptome- and proteome-oriented identification of dysregulated eIF4G, STAT3, and Hippo pathways altered by PIK3CA H1047R in HER2/ER-positive breast cancer. Article Snippet: Purpose Phosphatidylinositol 3-kinase (PI3K)/AKT pathway aberrations are common in human breast cancer.. Furthermore, PIK3CA mutations are commonly associated with resistance to anti-epidermal growth factor receptor 2 (HER2) or anti-estrogen receptor (ER) agents in HER2 or ER positive (HER2/ER) breast cancer.. Hence, deciphering the underlying mechanisms of PIK3CA mutations in HER2/ER breast cancer would provide novel insights into elucidating resistance to anti-HER2/ER therapies. 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