Expression of antioxidant enzymes in diseases of the human pancreas: Another link between chronic pancreatitis and pancreatic cancer

被引:108
作者
Cullen, JJ
Mitros, FA
Oberley, LW
机构
[1] Univ Iowa, Coll Med, Dept Surg, Iowa City, IA 52242 USA
[2] Univ Iowa, Coll Med, Dept Pathol, Iowa City, IA 52242 USA
[3] Univ Iowa, Coll Med, Dept Radiat Oncol, Iowa City, IA 52242 USA
关键词
pancreatic cancer; superoxide dismutase; pancreatitis; catalase; glutathione peroxidase;
D O I
10.1097/00006676-200301000-00005
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Introduction: Chronic pancreatitis is a significant risk factor for pancreatic cancer and is associated with the generation of reactive oxygen species. Cells contain a large number of antioxidants to prevent or repair the damage caused by reactive oxygen species. There are three major types of primary intracellular antioxidant enzymes in mammalian cells: superoxide dismutase (SOD), catalase, and peroxidase, of which glutathione peroxidase is the most prominent. Aim: To determine the level of antioxidant enzymes in human pancreas from normal, chronic pancreatitis, and pancreatic cancer specimens. Methodology: Immunohistochemical analysis for manganese SOD, copper/zinc SOD, catalase, and glutathione peroxidase expression using the avidin-biotin-peroxidase complex method was performed on pancreatic specimens previously fixed in formalin and embedded in paraffin. A quantitative digital imaging methodology was used to examine antioxidant staining in the pancreatic tissue. Cytoplasmic regions of ductal and acinar cells were identified and digitized. Mean gray-level pixel values were then obtained for each of these regions. Results: Cytoplasmic values of manganese SOD, catalase, and glutathione peroxidase were decreased in pancreatic cells from chronic pancreatitis specimens when compared with normal pancreas. In pancreatic carcinoma specimens, mean cytoplasmic gray-level values of all antioxidant enzymes were decreased when compared with normal pancreas. Conclusion: There appears to be a gradual decrease in antioxidant enzyme expression in pancreatic cells from normal pancreas to chronic pancreatitis to pancreatic cancer.
引用
收藏
页码:23 / 27
页数:5
相关论文
共 25 条
[11]   DETECTION OF POINT MUTATIONS IN THE KIRSTEN-RAS ONCOGENE PROVIDES EVIDENCE FOR THE MULTICENTRICITY OF PANCREATIC-CARCINOMA [J].
MOTOJIMA, K ;
URANO, T ;
NAGATA, Y ;
SHIKU, H ;
TSURIFUNE, T ;
KANEMATSU, T .
ANNALS OF SURGERY, 1993, 217 (02) :138-143
[12]   ROLE OF ANTIOXIDANT ENZYMES IN CELL IMMORTALIZATION AND TRANSFORMATION [J].
OBERLEY, LW ;
OBERLEY, TD .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 1988, 84 (02) :147-153
[13]  
OBERLEY LW, 1979, CANCER RES, V39, P1141
[14]  
OBERLEY LW, 1983, SUPEROXIDE DISMUTASE, V2
[15]  
Oberley LW, 1986, Free radicals, aging, and degenerative diseases, P325
[16]  
OBERLEY LW, 1994, DRUGS DIET DIS, V1, P49
[17]  
OBERLEY TD, 1993, FREE RADICALS AGING, P248
[18]   Analysis of K-ras oncogene mutations in chronic pancreatitis with ductal hyperplasia [J].
Rivera, JA ;
Rall, CJN ;
GraemeCook, F ;
FernandezdelCastillo, C ;
Shu, P ;
Lakey, N ;
Tepper, R ;
Rattner, DW ;
Warshaw, AL ;
Rustgi, AK .
SURGERY, 1997, 121 (01) :42-49
[19]   THE ROLE OF OXYGEN-DERIVED FREE-RADICALS IN THE PATHOGENESIS OF ACUTE-PANCREATITIS [J].
SANFEY, H ;
BULKLEY, GB ;
CAMERON, JL .
ANNALS OF SURGERY, 1984, 200 (04) :405-413
[20]   OXYGEN-TOXICITY IN CONTROL AND H2O2-RESISTANT CHINESE HAMSTER FIBROBLAST CELL-LINES [J].
SPITZ, DR ;
ELWELL, JH ;
SUN, Y ;
OBERLEY, LW ;
OBERLEY, TD ;
SULLIVAN, SJ ;
ROBERTS, RJ .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1990, 279 (02) :249-260