Reactive Nitrogen Species in Colon Carcinogenesis

被引:43
作者
Payne, Claire M. [1 ]
Bernstein, Carol [1 ]
Bernstein, Harris [1 ]
Gerner, Eugene W. [2 ]
Garewal, Harinder [3 ,4 ]
机构
[1] Univ Arizona, Coll Med, Dept Microbiol & Immunol, Tucson, AZ 85724 USA
[2] Univ Arizona, Coll Med, Dept Radiat Oncol, Tucson, AZ 85724 USA
[3] Univ Arizona, Coll Med, Dept Internal Med, Tucson, AZ 85724 USA
[4] Vet Affairs Hosp, Tucson, AZ 85724 USA
关键词
D O I
10.1089/ars.1999.1.4-449
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The role of reactive nitrogen species (RNS) in colon carcinogenesis is multifactorial and affects such as proliferation, apoptosis, differentiation, tumorigenesis, and metastases. This review describes the stages in colon carcinogenesis where nitric oxide (NO) and inducible NO synthase (NOS2) may influence the progression of a normal mucosa to overt metastatic cancer. Overexpression of NOS2 and an increase in the generation of NO and other RNS may lead to apoptosis resistance, DNA damage, mutation, up-regulation of COX-2, increased proliferation, an increase in oxidative stress and an increase in tumor vascularity and metastatic potential. Therefore, future goals are to establish mechanistically based biomarkers to assess individuals at risk for colon cancer and to implement chemopreventive and dietary strategies that reduce colon cancer risk. An understanding of NO signaling pathways in colon epithelial cells should provide the basis for novel biomarker development. Colon cancer prevention may be achieved effectively by chemically interfering with key components of the NO signaling pathways, changing dietary habits to reduce fat and increase antioxidant-containing vegetables, and dietary supplementation to increase DNA repair. Antiox. Redox Signal. 1, 449-467.
引用
收藏
页码:449 / 467
页数:19
相关论文
共 159 条
[21]   Nitric oxide and its role in apoptosis [J].
Brüne, B ;
von Knethen, A ;
Sandau, KB .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1998, 351 (03) :261-272
[22]  
Brune B, 1998, BIOCHEMISTRY-MOSCOW+, V63, P817
[23]   Deregulation of apoptosis in colorectal carcinoma: Theoretical and therapeutic implications [J].
Butler, LM ;
Hewett, PJ ;
Fitridge, RA ;
Cowled, PA .
AUSTRALIAN AND NEW ZEALAND JOURNAL OF SURGERY, 1999, 69 (02) :88-94
[24]  
Calmels S, 1997, CANCER RES, V57, P3365
[25]   Bile acid induced colonic irritation stimulates intracolonic nitric oxide release in humans [J].
Casellas, F ;
Mourelle, M ;
Papo, M ;
Guarner, F ;
Antolin, M ;
Armengol, JR ;
Malagelada, JR .
GUT, 1996, 38 (05) :719-723
[26]   EFFECTS OF 3 DIETARY PHYTOCHEMICALS FROM TEA, ROSEMARY AND TURMERIC ON INFLAMMATION-INDUCED NITRITE PRODUCTION [J].
CHAN, MMY ;
HO, CT ;
HUANG, HI .
CANCER LETTERS, 1995, 96 (01) :23-29
[27]   Cyclooxygenase inhibition decreases nitric oxide synthase activity in human platelets [J].
Chen, LY ;
Salafranca, MN ;
Mehta, JL .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1997, 273 (04) :H1854-H1859
[28]  
Chiarugi V, 1998, INT J MOL MED, V2, P715
[29]   gamma-Tocopherol traps mutagenic electrophiles such as NOx and complements alpha-tocopherol: Physiological implications [J].
Christen, S ;
Woodall, AA ;
Shigenaga, MK ;
SouthwellKeely, PT ;
Duncan, MW ;
Ames, BN .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (07) :3217-3222
[30]   Effects of selenium supplementation for cancer prevention in patients with carcinoma of the skin a randomized controlled trial - A randomized controlled trial [J].
Clark, LC ;
Combs, GF ;
Turnbull, BW ;
Slate, EH ;
Chalker, DK ;
Chow, J ;
Davis, LS ;
Glover, RA ;
Graham, GF ;
Gross, EG ;
Krongrad, A ;
Lesher, JL ;
Park, HK ;
Sanders, BB ;
Smith, CL ;
Taylor, JR .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1996, 276 (24) :1957-1963