首页 | 本学科首页   官方微博 | 高级检索  
   检索      


Enhanced expression of group II phospholipase A2 in human hepatocellular carcinoma
Authors:Zhao Ying  Hiromasa Tojo  Takanori Komatsubara  Manabu Nakagawa  Masami Inada  Sumio Kawata  Yuji Matsuzawa  Mitsuhiro Okamoto
Institution:1. Department of Molecular Physiology Chemistry, Osaka University Medical School, 2-2 Yamada-oka, Suita, Osaka 565, Japan;2. Second Department of Internal Medicine, Osaka University Medical School, 2-2 Yamada-oka, Suita, Osaka 565, Japan
Abstract:Enzyme activity, protein contents, and mRNA contents of group II phospholipase A2 (PLA2) in hepatocellular carcinoma (HCC) surgically obtained from 8 patients were compared with those in either its neighboring liver tissues or control liver tissues. The PLA2 specific activity towards the mixed micelles of 1-palmitoyl-2-oleoyl-phosphatidylglycerol and cholate was significantly greater in the tumor tissues (6.62 ± 1.46 nmol/min/mg) than those in the surrounding liver tissues (1.33 ± 0.22 nmol/min/mg) and controls (0.43 ± 0.04 nmol/min/mg). The results of immunoblot analysis using a specific anti-human group II PLA2 antibody and of Northern blot analysis using a human group II PLA2 cDNA as a probe demonstrated that group II PLA2 was responsible for the increased enzyme activity. The contents of immunoreactive group II PLA2 in the tumor tissues (8.81 ± 1.24 ng/mg) were significantly higher than those in the surrounding liver tissues (1.77 ± 0.27 ng/mg); those in the control tissues were below the analytical range of the method used. The group II PLA2 mRNA was also significantly increased in the tumor tissues, compared with that in the surrounding liver tissues, whereas it was not detectable in th controls. This indicates that group II PLA2 in HCC is induced at the pretranslational level.
Keywords:Human hepatocellular carcinoma  Phosphatidylglycerol  Overexpression  HCC  hepatovcellular carcinoma  POPG  1-palmitoyl-2-oleoyl-sn-glycerol-3-phosphoglycerol  TGF  transforming growth factor
本文献已被 ScienceDirect 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号