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World J Hepatol. Sep 27, 2010; 2(9): 337-344
Published online Sep 27, 2010. doi: 10.4254/wjh.v2.i9.337
Nitric oxide and cancer
Jordi Muntané, Manuel De la Mata
Jordi Muntané, Liver Research Unit, Maimonides Institute for Biomedical Research of Cordoba (IMIBIC), “Reina Sofia” University Hospital, Cordoba E-14004, Spain
Jordi Muntané, Manuel De la Mata, Biomedical Research Network Center for Liver and Digestive Diseases (CIBERehd), Cordoba E-14004, Spain
Manuel De la Mata, Digestive Clinical Unit, Maimonides Institute for Biomedical Research of Cordoba (IMIBIC), “Reina Sofia” University Hospital, Cordoba E-14004, Spain
Author contributions: Muntané J wrote the manuscript and De la Mata M revised it.
Correspondence to: Jordi Muntané, PhD, Liver Research Unit, “Reina Sofia” University Hospital, Av. Menéndez Pidal s/n, Cordoba E-14004, Spain. jordi.muntane.exts@juntadeandalucia.es
Telephone: +34-957-011070 Fax: +34-957-010452
Received: June 18, 2010
Revised: September 2, 2010
Accepted: September 9, 2010
Published online: September 27, 2010
Abstract

Nitric oxide (NO) is a lipophilic, highly diffusible and short-lived physiological messenger which regulates a variety of important physiological responses including vasodilation, respiration, cell migration, immune response and apoptosis. NO is synthesized by three differentially gene-encoded NO synthase (NOS) in mammals: neuronal NOS (nNOS or NOS-1), inducible NOS (iNOS or NOS-2) and endothelial NOS (eNOS or NOS-3). All isoforms of NOS catalyze the reaction of L-arginine, NADPH and oxygen to NO, L-citrulline and NADP. NO may exert its cellular action by cGMP-dependent as well as by cGMP-independent pathways including postranslational modifications in cysteine (S-nitrosylation or S-nitrosation) and tyrosine (nitration) residues, mixed disulfide formation (S-nitrosoglutathione or GSNO) or promoting further oxidation protein stages which have been related to altered protein function and gene transcription, genotoxic lesions, alteration of cell-cycle check points, apoptosis and DNA repair. NO sensitizes tumor cells to chemotherapeutic compounds. The expression of NOS-2 and NOS-3 has been found to be increased in a variety of human cancers. The multiple actions of NO in the tumor environment is related to heterogeneous cell responses with particular attention in the regulation of the stress response mediated by the hypoxia inducible factor-1 and p53 generally leading to growth arrest, apoptosis or adaptation.

Keywords: Nitric oxide; Cancer; Carcinogenesis