Literature DB >> 15476855

Nitric oxide signaling in colon cancer chemoprevention.

Chinthalapally V Rao1.   

Abstract

Nitric oxide (NO) is a pleiotrophic regulator, pivotal to numerous biological processes, including vasodilation, neurotransmission, and macrophage-mediated immunity. The highly reactive free radicals, produced by NO synthases (NOS) have been implicated in the modulation of carcinogenesis. Over-expression of inducible NOS (iNOS), a common phenomenon during chronic inflammatory conditions, generates sustainable amounts of NO, that its reactive intermediates are mutagenic, causing DNA damage or impairment of DNA repair, has been well established in carcinogenesis. Recent studies also implicate NO as having a key signaling molecule that regulates processes of tumorigenesis. Increased expression of iNOS has been observed in tumors of the colon, lung, oropharynx, reproductive organs, breast, and central nervous system besides its occurrence in chronic inflammatory diseases. Progression of a large majority of human and experimental colon tumors appears to progress by NO resulting from stimulation of proinflammatory cytokines, and inactivation (nitrosylation) of p53 mediated caspase activities in the tumors, whereas in some cases it associated with induction of apoptosis and tumor regression. This dichotomy is largely explained by the complexity of signaling pathways in tumor cells, that respond to NO very differently depending on its concentration. p53 mutation, functional loss, activation, and inactivation of apoptotic proteins all have been linked with NO resistance and dependence. Evidence from both in vitro and in vivo experiments support that NO and its reactive metabolite peroxynitrite stimulate COX-2 activity leading generation of tumor growth enhancing prostaglandins. Thus, NO mediated signaling can augment the tumor growth and metastasis by promoting invasive and angiogenic properties of tumor cells, which includes triggering and activation of COX-2. Thus, developing selective inhibitors of iNOS and NO-releasing agents may lead to important strategies for chemoprevention of colon cancer. Chemoprevention studies at preclinical level with several selective inhibitors of iNOS in both chemically and transgenic models of colon cancer are encouraging.

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Year:  2004        PMID: 15476855     DOI: 10.1016/j.mrfmmm.2004.05.022

Source DB:  PubMed          Journal:  Mutat Res        ISSN: 0027-5107            Impact factor:   2.433


  47 in total

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2.  Kimchi protects against azoxymethane/dextran sulfate sodium-induced colorectal carcinogenesis in mice.

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3.  Melanoma prevention using topical PBISe.

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Journal:  Cancer Prev Res (Phila)       Date:  2011-03-02

4.  Suppression of the tumorigenic phenotype in human oral squamous cell carcinoma cells by an ethanol extract derived from freeze-dried black raspberries.

Authors:  Kapila A Rodrigo; Yeshwant Rawal; Robert J Renner; Steven J Schwartz; Qingguo Tian; Peter E Larsen; Susan R Mallery
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6.  The effects of NOS3 Glu298Asp variant on colorectal cancer risk and progression in Turkish population.

Authors:  Soykan Arıkan; Canan Cacina; Erkan Guler; Serdar Çulcu; Gulay Tuna; Ilhan Yaylım-Eraltan
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7.  Role of Hepatocyte Paraffin 1 antigen in the course of colorectal carcinogenesis.

Authors:  Riham M Abu-Zeid; Rola M Farid
Journal:  Int J Physiol Pathophysiol Pharmacol       Date:  2013-09-10

Review 8.  Diet and supplements and their impact on colorectal cancer.

Authors:  Marinos Pericleous; Dalvinder Mandair; Martyn E Caplin
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9.  Chemoprevention of Colon Cancer by iNOS-Selective Inhibitors.

Authors:  Naveena B Janakiram; Chinthalapally V Rao
Journal:  For Immunopathol Dis Therap       Date:  2012-01-01

10.  Hesperidin alleviates oxidative stress and downregulates the expressions of proliferative and inflammatory markers in azoxymethane-induced experimental colon carcinogenesis in mice.

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Journal:  Inflamm Res       Date:  2013-02-02       Impact factor: 4.575

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