Expression of inducible nitric oxide synthase and p53 in oral epithelial dysplasia

被引:35
作者
Brennan, PA
Conroy, B
Spedding, AV
机构
[1] St Richards Hosp, Chichester, England
[2] Queen Alexandra Hosp, Portsmouth, Hants, England
来源
ORAL SURGERY ORAL MEDICINE ORAL PATHOLOGY ORAL RADIOLOGY AND ENDODONTOLOGY | 2000年 / 90卷 / 05期
关键词
D O I
10.1067/moe.2000.108800
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Aims. Nitric oxide (NO) has been studied in a variety of human cancers and is implicated in both tumor promotion and inhibition. Downregulation of the enzyme iNOS by wild-type p53 (but not mutant) protein has been shown to occur in normal cells and some tumors, but the relationship has not been reported in oral epithelial dysplasia. Methods and results. An immunohistochemical study was conducted with antibodies to iNOS and p53 (clone DO-7) in 36 cases of oral dysplasia of varying severity. Statistical analysis showed a significant correlation between iNOS staining and grade of dysplasia (P < .001) and between p53 and iNOS staining (P < .001). Conclusions. This preliminary study has shown that iNOS expression correlates with severity of dysplasia, and it is also increased in those cases showing positive staining for p53. Further research is required to fully establish the relationship between iNOS and p53 in both dysplasia and oral squamous cell carcinoma.
引用
收藏
页码:624 / 629
页数:6
相关论文
共 29 条
[1]   Up-regulation of inducible nitric oxide synthase expression in cancer-prone p53 knockout mice [J].
Ambs, S ;
Ogunfusika, MO ;
Merriam, WG ;
Bennett, WP ;
Billiar, TR ;
Harris, CC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (15) :8823-8828
[2]   Interactive effects of nitric oxide and the p53 tumor suppressor gene in carcinogenesis and tumor progression [J].
Ambs, S ;
Hussain, SP ;
Harris, CC .
FASEB JOURNAL, 1997, 11 (06) :443-448
[3]   Nitric oxide synthase type 3 is increased in squamous hyperplasia, dysplasia, and squamous cell carcinoma of the head and neck [J].
Bentz, BG ;
Haines, GK ;
Lingen, MW ;
Pelzer, HJ ;
Hanson, DG ;
Radosevich, JA .
ANNALS OF OTOLOGY RHINOLOGY AND LARYNGOLOGY, 1999, 108 (08) :781-787
[4]   Expression of nitric oxide synthase in pleomorphic adenomas of the parotid [J].
Brennan, PA ;
Umar, T ;
Bunckley, J ;
Zaki, GA ;
Langdon, JD ;
Spedding, A ;
Peters, W .
BRITISH JOURNAL OF ORAL & MAXILLOFACIAL SURGERY, 2000, 38 (04) :338-342
[6]   ELEVATED P53 EXPRESSION CORRELATES WITH A HISTORY OF HEAVY SMOKING IN SQUAMOUS-CELL CARCINOMA OF THE HEAD AND NECK [J].
FIELD, JK ;
SPANDIDOS, DA ;
MALLIRI, A ;
GOSNEY, JR ;
YIAGNISIS, M ;
STELL, PM .
BRITISH JOURNAL OF CANCER, 1991, 64 (03) :573-577
[7]   Nitric oxide-induced p53 accumulation and regulation of inducible nitric oxide synthase expression by wild-type p53 [J].
Forrester, K ;
Ambs, S ;
Lupold, SE ;
Kapust, RB ;
Spillare, EA ;
Weinberg, WC ;
FelleyBosco, E ;
Wang, XW ;
Geller, DA ;
Tzeng, E ;
Billiar, TR ;
Harris, CC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (06) :2442-2447
[8]  
FORSTERMANN U, 1995, N-S ARCH PHARMACOL, V352, P351
[9]   Role of nitric oxide in angiogenesis and tumor progression in head and neck cancer [J].
Gallo, O ;
Masini, E ;
Morbidelli, L ;
Franchi, A ;
Fini-Storchi, I ;
Vergari, WA ;
Ziche, M .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1998, 90 (08) :587-596
[10]   Nitric oxide synthase activity in human squamous cell carcinoma of the head and neck [J].
Gavilanes, J ;
Moro, MA ;
Lizasoain, I ;
Lorenzo, P ;
Pérez, A ;
Leza, JC ;
Alvarez-Vicent, JJ .
LARYNGOSCOPE, 1999, 109 (01) :148-152