ABSTRACT
@#【Objective】To investigate the effect of Imatinib（Ima）on the inflammatory phenotype of RAW264.7 mac⁃ rophages induced by lipopolysaccharide（LPS）.【Methods】RAW264.7 cells were treated by LPS（0.1 μg/mL）and/or Ima（1 μmol/L，5 μmol/L）. The mRNA levels of IL-1β，IL-10，CCL2，iNOS，TNF-α and Arg1 in RAW264.7 cells were tested by Q-PCR. The iNOS protein level and the activation of NF-κB and MAPK signal pathways were detected by Western Blot. The protein levels of IL-1β，CCL2，IL-10 and TNF-α in cell supernatant were detected by ELISA. 【Results】Compared with the normal control group，the mRNA levels of IL-1β，CCL2，iNOS，TNF-α and IL-10 were significantly increased in RAW264.7 cells treated with LPS for 8 h（P < 0.001）. In addition，the cell supernatant protein levels of IL-1β，IL-10，CCL2 as well as TNFα and the iNOS protein level were significantly increased in RAW264.7 cells stimulated by LPS for 24 h（P < 0.001）. Moreover，the phosphorylation levels of p65，p38，ERK and AKT were enhanced in RAW264.7 cells after treatment with LPS for 24 h. Compared with LPS group，pretreatment with Ima decreased the mRNA and protein levels of IL-1β，CCL2，iNOS and TNF-α（P < 0.01，P < 0.001），but increased the mRNA and protein level of IL-10（P < 0.001）. And this effect of Ima was dose-dependent. The phosphorylation levels of p65，p38， ERK and AKT were decreased in LPS+Ima group compared with that in LPS group. The functional status of RAW264.7 cells did not change significantly after treatment with Ima alone.【Conclusions】The effect of Imatinib to inhibit the inflammato⁃ ry phenotype of macrophage is related to retarding the overactivation of NF-κB and MAPK signaling pathways.
ABSTRACT
Objective@#To investigate the expressions of glutathione S-transferase (GSTP1) and tetra-hydroxynonenal (4-HNE) in prostate cancer (PCa) and their clinical significance.@*METHODS@#We determined the expressions of GSTP1 and 4-HNE in 40 patients with PCa and another 42 with benign prostatic hyperplasia (BPH) by immunohistochemistry and analyzed their relationship with Gleason grades.@*RESULTS@#The expression rate of GSTP1 was 92.9% in the BPH tissue, and those in the highly, moderately, and lowly differentiated PCa tissues were 58.3%, 20.0%, and 16.7%, respectively, significantly higher in the BPH than in the PCa group (P <0.01). However, the positive rate of 4-HNE was only 5.0% in the BPH tissue, markedly lower than 91.6%, 100.0%, and 100.0% in the highly, moderately, and lowly differentiated PCa tissues (P <0.01). There was a negative correlation between the expression of GSTP1 and that of 4-HNE in the PCa tissue (r = －2.73, P <0.01).@*CONCLUSIONS@#Expression deletion of GSTP1 and high expression of 4-HNE may play an important role in the progression of prostate cancer.