11 research outputs found

    Supplemental Table S2

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    Supplemental Table 2. Top 10 significantly (p<0.05) enriched Ingenuity Canonical Pathways for the 193 transcripts that were differentially expressed in the HFD:control comparison of liver transcriptomes but not the HFD+DHA:control comparison (total of 24 enriched pathways), and for the 179 transcripts differentially expressed in the HFD+DHA:control comparison of liver transcriptomes, but not the HFD:Control comparison (total of 16 enriched pathways). Transcriptomic analysis was performed on N=4 for each group. Ratio = number of differentially expressed genes/total genes in pathway. Red indicates predicted positive activation of the pathway and upregulation of an individual transcript and blue indicates downregulation.</p

    Supplemental Table S5

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    Supplemental Table 5. Top 10 significantly (p<0.05) enriched Ingenuity Canonical Pathways for the 76 transcripts that were differentially expressed in the HFD:control comparison of skeletal muscle transcriptomes but not the HFD+EPA:control comparison (total of 21 enriched pathways), and for the 216 transcripts differentially expressed in the HFD+EPA:control comparison of skeletal muscle transcriptomes, but not the HFD:Control comparison (total of 116 enriched pathways). Transcriptomic analysis was performed on N=4 for each group. Ratio = number of differentially expressed genes/total genes in pathway. Red indicates predicted positive activation of the pathway and upregulation of an individual transcript and blue indicates downregulation.</p

    Supplemental Table S4

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    Supplemental Table 4. Top 10 significantly (p<0.05) enriched Ingenuity Canonical Pathways for the 152 transcripts that were differentially expressed in the HFD:control comparison of skeletal muscle transcriptomes but not the HFD+DHA:control comparison (total of 59 enriched pathways), and for the 67 transcripts differentially expressed in the HFD+DHA:control comparison of skeletal muscle transcriptomes, but not the HFD:Control comparison (total of 44 enriched pathways). Transcriptomic analysis was performed on N=4 for each group. Ratio = number of differentially expressed genes/total genes in pathway. Red indicates predicted positive activation of the pathway and upregulation of an individual transcript and blue indicates downregulation.</p

    Supplemental Table S6

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    Supplemental Table 6. Top 10 significantly (p-value <0.05) enriched Ingenuity Canonical Pathways in the HFD:HFD+DHA (14 total enriched pathways), the HFD:HFD+EPA (9 enriched pathways), and the HFD+DHA:HFD+EPA (15 enriched pathways) comparisons of liver transcriptomes. Transcriptomic analysis was performed on N=4 for each group. Ratio = number of differentially expressed genes/total genes in pathway. Red indicates predicted positive activation of the pathway and upregulation of an individual transcript in the reference group (listed first) and blue indicates downregulation.</p

    Supplemental Table S3

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    Supplemental Table 3. Top 10 significantly (p<0.05) enriched Ingenuity Canonical Pathways for the 92 transcripts that were differentially expressed in the HFD:control comparison of liver transcriptomes but not the HFD+EPA:control comparison (total of 25 enriched pathways), and for the 264 transcripts differentially expressed in the HFD+EPA:control comparison of liver transcriptomes, but not the HFD:Control comparison (total of 33 enriched pathways). Transcriptomic analysis was performed on N=4 for each group. Ratio = number of differentially expressed genes/total genes in pathway. Red indicates predicted positive activation of the pathway and upregulation of an individual transcript and blue indicates downregulation.</p

    Supplemental Table S7

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    Supplemental Table 7. Top 10 significantly (p-value <0.05) enriched Ingenuity Canonical Pathways in the HFD:HFD+DHA (39 total enriched pathways), the HFD:HFD+EPA (5 total enriched pathways), and the HFD+DHA:HFD+EPA (61 enriched pathways) comparisons of skeletal muscle transcriptomes. Transcriptomic analysis was performed on N=4 for each group. Ratio = number of differentially expressed genes/total genes in pathway. Red indicates predicted positive activation of the pathway and upregulation of an individual transcript and blue indicates downregulation.</p

    Supplemental Table S1

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    Supplemental Table 1. Dietary composition of the purified diets for the control, HFD, HFD+EPA, and HFD+DHA groups

    Supplemental File 1: Plasma Metabolites

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    Comparison of metabolites identified in the plasma of patients with cancer and healthy age-, sex-, and BMI-matched control participants. Fold-change analyses and unpaired t-tests were performed for each identified metabolite to identify differences in the relative abundance of individual metabolites between patients with cancer and control participants. p-values were false discovery rate (FDR)-adjusted to account for multiple comparisons Fold change (FC) analysis is defined as cancer/control, where a negative Log2(FC) indicates lower abundance in patients with cancer

    Supplemental Figure 1. Plasma enrichments of stable isotope amino acid tracers

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    The mean plasma enrichment (MPE) of 13C6 phenylalanine, 13C6 tyrosine, and 15N tyrosine measured by gas chromatography/mass spectrometry (GCMS) in patients with cancer and in healthy age-, sex- and BMI-matched control participants during a primed, continuous infusion of 13C6 phenylalanine and 15N tyrosine.</p

    Supplemental Table 1. Estimated food intake based on the VioCare Food Frequency Questionnaire

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    Estimated food intake for patients with cancer and healthy age-, sex-, and BMI-matched control participants based on the VioCare Food Frequency Questionnaire.</p
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