Inflammatory cytokines, appetite-regulating hormones, and energy metabolism in patients with gastrointestinal cancer
by Stacey
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This study investigated the energy metabolism and its relationship with inflammatory cytokines and hormones that regulate appetite in patients with gastrointestinal cancer. Subjects are inpatients scheduled to undergo intervention therapies for gastrointestinal cancers diagnosed. The nutritional status on admission assessed based on anthropometric measurements, nutritional screening results, levels of dietary intake (energy intake / energy provided in hospital food), and the results of biochemical tests. Fat-free mass (FFM) was measured using bioelectrical impedance analysis. Resting energy expenditure (REE) and respiratory quotient were measured by indirect calorimetry, and basal energy expenditure (BEE) is calculated using the Harris-Benedict equation.
A total of 51 patients with gastrointestinal cancer were enrolled (17 with esophageal cancer, 15 with gastric cancer, and 19 with colorectal cancer); 16 had stage I disease, 11 had stage II, 13 had stage III and 11 stage IV had. Levels of inflammatory cytokines such as interleukin ( IL ) – 6 and tumor necrosis factor (TNF) -α increased significantly with the development stage of the cancer (P <0.001; Jonckheere-Terpstra trend test ). REE / weight and REE / FFM tended to increase with the development stage of the cancer (P = 0.064 and P = 0.053, respectively; Jonckheere-Terpstra trend test). FFM showed a significant negative correlation with TNF-α levels (P = 0.008; Spearman correlation coefficient).
Also, the rate of food intake showed a significant negative correlation with the level of IL -6 and TNF-α (P <0.001). Active ghrelin levels were positively correlated with that of IL -6 and energy metabolism (P = 0.004 and 0.0 16 , respectively) and negatively correlated with the level of food intake ( P = 0.035), indicating the resistance state of ghrelin. In conclusion, this study confirms that the increase levels of inflammatory cytokines in the development of gastrointestinal cancer and suggest possible increase in association with a decrease in FFM and improve energy metabolism. However, the increase failed to offset the active ghrelin levels in patients with cancer cachexia.
Whole-blood mRNA expression and glucocorticoid-related inflammasome- completely separate patient-treatment-resistant depressed patients drug free and responsive in the study BIODEP MRNA expression signature associated with the ‘pro-inflammatory’ phenotype depression, and signatures associated differential subtype of depression and antidepressant effects, is still unknown. We studied 130 patients with depression (58 treatment-resistant, 36 antidepressant-responsive and 36 at this time is not treated) and 40 healthy controls from studies BIODEP, and use whole blood mRNA qPCR to measure the expression of 16 candidate mRNA , some never measured before: interleukin ( IL ) – 1-beta, IL -6, TNF-alpha, macrophage inhibiting factor (MIF ), the glucocorticoid receptor (GR), SGK1, FKBP5, which P2RX7 receptor purinergic, CCL2, CXCL12, c-reactive protein (CRP), alpha-2-macroglobulin (A2M), acquaporin-4 (AQP4), ISG15, STAT1 and USP -18. All genes but AQP4, ISG15 and USP-18 were differentially regulated.
Treatment-resistant and drug-free depressed patients have both increased activation of the inflammasome (P2RX7 higher and proinflammatory cytokines / chemokines mRNA expression) and resistance to glucocorticoids (lowering GR and higher expression of FKBP5 mRNA), whereas patients unresponsive have phenotypes medium, too , lower CXCL12.
Description: A sandwich quantitative ELISA assay kit for detection of Chicken Interleukin 16 (IL16) in samples from serum, plasma or other biological fluids.
Description: A sandwich quantitative ELISA assay kit for detection of Chicken Interleukin 16 (IL16) in samples from serum, plasma or other biological fluids.
Description: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Chicken IL16. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Chicken IL16. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Chicken IL16, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Chicken IL16 in the samples is then determined by comparing the OD of the samples to the standard curve.
Description: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Chicken IL16. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Chicken IL16. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Chicken IL16, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Chicken IL16 in the samples is then determined by comparing the OD of the samples to the standard curve.
Description: This CD Interleukin 2 ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Human IL-2. This ELISA kit for research use only, not for therapeutic or diagnostic applications!
Description: This CD Interleukin 4 ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Human IL-4. This ELISA kit for research use only, not for therapeutic or diagnostic applications!
Description: Quantitativecompetitive ELISA kit for measuring Chicken Interleukin 8 (IL-8) in samples from serum, plasma, tissue homogenates. A new trial version of the kit, which allows you to test the kit in your application at a reasonable price.
Description: Quantitativecompetitive ELISA kit for measuring Chicken Interleukin 8(IL-8) in samples from serum, plasma, tissue homogenates. Now available in a cost efficient pack of 5 plates of 96 wells each, conveniently packed along with the other reagents in 5 separate kits.
Description: Quantitativesandwich ELISA kit for measuring Chicken Interleukin 3, IL-3 in samples from serum, plasma, tissue homogenates. A new trial version of the kit, which allows you to test the kit in your application at a reasonable price.
Description: Quantitativesandwich ELISA kit for measuring Chicken Interleukin 3, IL-3 in samples from serum, plasma, tissue homogenates. Now available in a cost efficient pack of 5 plates of 96 wells each, conveniently packed along with the other reagents in 5 separate kits.
Description: Quantitativecompetitive ELISA kit for measuring Chicken Interleukin 9, IL-9 in samples from serum, plasma, tissue homogenates. A new trial version of the kit, which allows you to test the kit in your application at a reasonable price.
Description: Quantitativecompetitive ELISA kit for measuring Chicken Interleukin 9, IL-9 in samples from serum, plasma, tissue homogenates. Now available in a cost efficient pack of 5 plates of 96 wells each, conveniently packed along with the other reagents in 5 separate kits.
Description: Quantitativecompetitive ELISA kit for measuring Chicken Interleukin 1, IL-1 in samples from serum, plasma, tissue homogenates. A new trial version of the kit, which allows you to test the kit in your application at a reasonable price.
Description: Quantitativecompetitive ELISA kit for measuring Chicken Interleukin 1, IL-1 in samples from serum, plasma, tissue homogenates. Now available in a cost efficient pack of 5 plates of 96 wells each, conveniently packed along with the other reagents in 5 separate kits.
Description: Quantitativesandwich ELISA kit for measuring Chicken Interleukin 6, IL-6 in samples from serum, plasma, tissue homogenates. A new trial version of the kit, which allows you to test the kit in your application at a reasonable price.
Description: Quantitativesandwich ELISA kit for measuring Chicken Interleukin 6, IL-6 in samples from serum, plasma, tissue homogenates. Now available in a cost efficient pack of 5 plates of 96 wells each, conveniently packed along with the other reagents in 5 separate kits.
Description: Quantitativesandwich ELISA kit for measuring Chicken Interleukin 2, IL-2 in samples from serum, plasma, tissue homogenates. A new trial version of the kit, which allows you to test the kit in your application at a reasonable price.
Description: Quantitativesandwich ELISA kit for measuring Chicken Interleukin 2, IL-2 in samples from serum, plasma, tissue homogenates. Now available in a cost efficient pack of 5 plates of 96 wells each, conveniently packed along with the other reagents in 5 separate kits.
Description: Quantitativesandwich ELISA kit for measuring Chicken Interleukin 4, IL-4 in samples from serum, plasma, tissue homogenates. A new trial version of the kit, which allows you to test the kit in your application at a reasonable price.
Description: Quantitativesandwich ELISA kit for measuring Chicken Interleukin 4, IL-4 in samples from serum, plasma, tissue homogenates. Now available in a cost efficient pack of 5 plates of 96 wells each, conveniently packed along with the other reagents in 5 separate kits.
The most interesting, using a binomial logistic model we found that the signatures of six mRNA (P2RX7, IL -1-beta, IL -6, TNF-alpha, CXCL12 and GR ) is distinguished from the treatment-resistant patient is responsive, even after adjusting for other variables that differ between the groups, such as trait- and anxiety states, a history of child abuse and serum CRP.