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Image Search Results
a " width="100%" height="100%">
Journal: Preventing Chronic Disease
Article Title: Genomics and the Prevention and Control of Common Chronic Diseases: Emerging Priorities for Public Health Action
doi:
Figure Lengend Snippet: Examples of News Stories on Human Genome Discoveries Relevant to Common Chronic Diseases
Article Snippet:
Techniques: Mutagenesis
Journal: bioRxiv
Article Title: Integrated RNA and metabolite profiling of urine liquid biopsies for prostate cancer biomarker discovery
doi: 10.1101/599514
Figure Lengend Snippet: (a) A heatmap showing expression of 37 significantly upregulated genes in cancer liquid biopsies. (b,c) Among 37 upregulated genes, 13 genes ( FH, SMARCB1, GRHPR, PHB, NACA, RPS11, RPL22, NPM1, EPCAM, TFG, HDAC6, ELK4, BRD3 ) were significantly upregulated in primary tumors (n=497) compared to normal (n=52) in TCGA data. In the heatmap, black dots next to the gene name mark the genes upregulated in primary tumor compare to normal in TCGA data. The TCGA project for PCa data is publicly available for download at https://portal.gdc.cancer.gov/projects/TCGA-PRAD . (d) These 13 genes were also tested in two prostate cancer cell lines (LNCaP and PC3), and most were overexpressed apart from NACA , which was downregulated in both cell lines; BRD3 and EPCAM , which were decreased in PC3 cells, and HDAC6 , which was downregulated in LNCaP cells. (e) Normalized Enrichment Score plot of the top 13 pathways in cancer urine. (f) Geneset Enrichment Score Plot (GSEA) of the TCA cycle (NES = 2.8, p-value = 0.0). (g) GSEA of the alanine, aspartate, and glutamate metabolism (NES = 2.42, p-value = 0.0). GSEA was conducted using GSEA software from the Broad Institute ( http://software.broadinstitute.org/gsea/index.jsp ).
Article Snippet:
Techniques: Expressing, Software
Journal: bioRxiv
Article Title: Integrated RNA and metabolite profiling of urine liquid biopsies for prostate cancer biomarker discovery
doi: 10.1101/599514
Figure Lengend Snippet: (a) GOT1 knockdown in LNCaP and PC3 prostate cancer cell lines. (b) GOT1 knockdown significantly inhibits cell viability in PC3 and LNCaP cells. (c) Invasion and (d) anchorage-independent growth in prostate cancer cell lines upon GOT1 knockdown. (e) GOT1 knockdown significantly increases ROS production in PC3 and LNCaP cells. The data from three independent experiments were expressed as mean ± SD.
Article Snippet:
Techniques: Knockdown