Correlated expression of inducible nitric oxide synthase and P53, Bax in benign and malignant diseased gallbladder

被引:13
作者
Zhang, M
Pan, JW
Ren, TR
Zhu, YF
Han, YJ
Kühnel, W
机构
[1] Zhejiang Univ, Dept Anat, Zhejiang 310006, Peoples R China
[2] Zhejiang Univ, Affiliated Hosp 1, Coll Med, Zhejiang 310006, Peoples R China
[3] Univ Lubeck, Dept Anat, D-23538 Lubeck, Germany
关键词
gallbladder adenocarcinoma; inducible nitric oxide synthase; P53; Bax; immunohistochemistry;
D O I
10.1016/S0940-9602(03)80125-5
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Our goal has been to investigate the expression and correlated significance of inducible nitric oxide synthase (iNOS) and P53, Bax in benign and malignant gallbladder diseases. We detected the expression of iNOS, P53 and Bax in the gallbladder wall by SP immunohistochemistry in 16 cases of chronic cholecystitis, 11 cases of chronic cholecystitis with adenomyoma and 24 cases of gallbladder adenocarcinoma. The percentage of positively marked tumor cells was counted under microscope and the intensity of immunoreactivity was graded. SPSS10.0 statistical software was applied for statistical analysis. In this study, we found that: (1) Both benign and malignant diseased gallbladder wall expressed iNOS and Bax. Compared to benign diseased gallbladders, their expression in adenocarinoma was decreased (p < 0.05), P53 was expressed strongly only in nuclei of adenocarcinoma cells of some cases. (2) In benign and malignant diseased gallbladders, iNOS expression was related positively to Bax (p < 0.01), the expression of P53 and Bax had a negative relationship (p < 0.01). The results suggested that both chronic cholecystitis and chronic cholecystitis with adenomyoma carry the risk of becoming malignant, especially the latter. NO is an important mediated molecule in cancer, there are intimate relationships between gallbladder cancer and apoptosis.
引用
收藏
页码:549 / 554
页数:6
相关论文
共 22 条
[1]   Vascular endothelial growth factor and nitric oxide synthase expression in human lung cancer and the relation to p53 [J].
Ambs, S ;
Bennett, WP ;
Merriam, WG ;
Ogunfusika, MO ;
Oser, SM ;
Khan, MA ;
Jones, RT ;
Harris, CC .
BRITISH JOURNAL OF CANCER, 1998, 78 (02) :233-239
[2]  
Calmels S, 1997, CANCER RES, V57, P3365
[3]   ABERRANT EXPRESSION OF NITRIC-OXIDE SYNTHASE IN HUMAN POLYPS, NEOPLASTIC COLONIC MUCOSA AND SURROUNDING PERITUMORAL NORMAL MUCOSA [J].
CHHATWAL, VJS ;
NGOI, SS ;
CHAN, STF ;
CHIA, YW ;
MOOCHHALA, SM .
CARCINOGENESIS, 1994, 15 (10) :2081-2085
[4]  
CUI SJ, 1994, CANCER RES, V54, P2462
[5]  
FURUNEN N, 2000, HISTOL HISTOPATHOL, V21, P53
[6]   Role of nitric oxide in tumour progression with special reference to a murine breast cancer model [J].
Jadeski, LC ;
Chakraborty, C ;
Lala, PK .
CANADIAN JOURNAL OF PHYSIOLOGY AND PHARMACOLOGY, 2002, 80 (02) :125-135
[7]   ROLES OF NITRIC-OXIDE IN TUMOR-GROWTH [J].
JENKINS, DC ;
CHARLES, IG ;
THOMSEN, LL ;
MOSS, DW ;
HOLMES, LS ;
BAYLIS, SA ;
RHODES, P ;
WESTMORE, K ;
EMSON, PC ;
MONCADA, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (10) :4392-4396
[8]  
JINSHENG S, 1998, CHI J HEPATOCHOL SUR, V4, P216
[9]   Neurogenic control of the ovine gallbladder: Ultrastructural and functional study [J].
Khoursheed, M ;
Krajci, D ;
Oriowo, MA ;
Philip, EK ;
Thulesius, O .
DIGESTION, 1998, 59 (04) :335-342
[10]   Inhibition of protein synthesis by nitric oxide correlates with cytostatic activity:: Nitric oxide induces phosphorylation of initiation factor eIF-2α [J].
Kim, YM ;
Son, K ;
Hong, SJ ;
Green, A ;
Chen, JJ ;
Tzeng, E ;
Hierholzer, C ;
Billiar, TR .
MOLECULAR MEDICINE, 1998, 4 (03) :179-190