The regulation of nitric oxide in tumor progression and therapy

J Int Med Res. 2020 Feb;48(2):300060520905985. doi: 10.1177/0300060520905985.

Abstract

Nitric oxide (NO) is a ubiquitous gas with free radical groups that is soluble in water, and which is involved in numerous physiological functions including inflammatory and immune responses. However, the role of NO in tumor biology is controversial and misunderstood. NO has been shown to have both anti-cancer and carcinogenic effects, which are dependent on the time, location, and concentration of NO. This duality presents a double challenge to determine the net impact of NO on cancer and to define the therapeutic role of NO-centered anti-cancer strategies. Nevertheless, it is believed that a comprehensive and dynamic understanding of the cascade of molecular and cellular events underlying tumor biology that are affected by NO will allow researchers to exploit the potential anti-tumor properties of drugs that interfere with NO metabolism.

Keywords: Nitric oxide; cancer; nitric oxide synthase; signaling; tumor; tumor therapy.

Publication types

  • Review

MeSH terms

  • Antineoplastic Agents / pharmacology
  • Antineoplastic Agents / therapeutic use*
  • Carcinogenesis / drug effects
  • Carcinogenesis / genetics
  • Carcinogenesis / pathology
  • Disease Progression
  • Epigenesis, Genetic
  • Gene Expression Regulation, Neoplastic / drug effects
  • Genetic Therapy / methods*
  • Humans
  • Neoplasms / genetics
  • Neoplasms / pathology
  • Neoplasms / therapy*
  • Nitric Oxide / agonists
  • Nitric Oxide / antagonists & inhibitors
  • Nitric Oxide / metabolism*
  • Nitric Oxide Donors / pharmacology
  • Nitric Oxide Donors / therapeutic use
  • Nitric Oxide Synthase Type II / genetics
  • Nitric Oxide Synthase Type II / metabolism
  • Nitric Oxide Synthase Type III / genetics
  • Nitric Oxide Synthase Type III / metabolism
  • Signal Transduction / drug effects
  • Time Factors

Substances

  • Antineoplastic Agents
  • Nitric Oxide Donors
  • Nitric Oxide
  • NOS2 protein, human
  • NOS3 protein, human
  • Nitric Oxide Synthase Type II
  • Nitric Oxide Synthase Type III