Nitric oxide synthase activity and expression in human colorectal cancer

被引:110
作者
Moochhala, S
Chhatwal, VJS
Chan, STF
Ngoi, SS
Chia, YW
Rauff, A
机构
[1] Department of Surgery, National University of Singapore, Singapore 0511
关键词
D O I
10.1093/carcin/17.5.1171
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The present study investigated the activity and cellular localization of individual isoenzymes of nitric oxide synthase (NOS) using immunohistochemistry and the [H-3]citrulline assay in normal colorectal epithelia and neoplastic tissue, Intracellular localization of isoenzymes of NOS was detectable by immunohistochemistry in normal epithelial cells, Colorectal adenocarcinomas had a marked reduction of both inducible NOS (iNOS) and constitutive NOS (cNOS) expression, Expression of iNOS was completely absent in tumour cells (P < 0.0001), while cNOS was reduced in 66% and absent in 34% of tumours studied when compared with controls (P < 0.0001), NOS activity using the [H-3]citrulline assay was detectable in normal epithelium and was found to be reduced in tumours (P < 0.001), In addition, colonic adenomas had reduced iNOS but not cNOS expression when compared with controls (P < 0.003 and P = 0.39 respectively), We conclude that NOS is present and active within the epithelium of the normal colon, with localization of the individual isoenzymes, Furthermore, there was loss of activity and expression of individual isoenzymes in colonic neoplasms.
引用
收藏
页码:1171 / 1174
页数:4
相关论文
共 18 条
[1]   INHIBITORS OF NITRIC-OXIDE SYNTHASE SELECTIVELY REDUCE FLOW IN TUMOR-ASSOCIATED NEOVASCULATURE [J].
ANDRADE, SP ;
HART, IR ;
PIPER, PJ .
BRITISH JOURNAL OF PHARMACOLOGY, 1992, 107 (04) :1092-1095
[2]   NITRIC-OXIDE MODULATES WATER AND ELECTROLYTE TRANSPORT IN THE ILEUM [J].
BARRY, MK ;
ALOISI, JD ;
PICKERING, SP ;
YEO, CJ .
ANNALS OF SURGERY, 1994, 219 (04) :382-388
[3]   NITRIC-OXIDE MEDIATES GLUTAMATE-LINKED ENHANCEMENT OF CGMP LEVELS IN THE CEREBELLUM [J].
BREDT, DS ;
SNYDER, SH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (22) :9030-9033
[4]   INDUCTION OF NITRIC-OXIDE SYNTHASE IN THE NEO-VASCULATURE OF EXPERIMENTAL-TUMORS IN MICE [J].
BUTTERY, LDK ;
SPRINGALL, DR ;
ANDRADE, SP ;
RIVEROSMORENO, V ;
HART, I ;
PIPER, PJ ;
POLAK, JM .
JOURNAL OF PATHOLOGY, 1993, 171 (04) :311-319
[5]   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
[6]   2ND MESSENGER ROLE FOR NO WIDENS TO NERVOUS AND IMMUNE-SYSTEMS [J].
COLLIER, J ;
VALLANCE, P .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1989, 10 (11) :427-431
[7]   HUMAN MONOCYTES/MACROPHAGES - NO OR NO NO [J].
DENIS, M .
JOURNAL OF LEUKOCYTE BIOLOGY, 1994, 55 (05) :682-684
[8]   MOLECULAR MECHANISMS OF NITRIC-OXIDE REGULATION - POTENTIAL RELEVANCE TO CARDIOVASCULAR-DISEASE [J].
DINERMAN, JL ;
LOWENSTEIN, CJ ;
SNYDER, SH .
CIRCULATION RESEARCH, 1993, 73 (02) :217-222
[9]  
DONG ZY, 1994, CANCER RES, V54, P789
[10]   NITRIC-OXIDE - A CYTO-TOXIC ACTIVATED MACROPHAGE EFFECTOR MOLECULE [J].
HIBBS, JB ;
TAINTOR, RR ;
VAVRIN, Z ;
RACHLIN, EM .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1988, 157 (01) :87-94