Literature DB >> 22202160

Nitroimidazole radiopharmaceuticals in hypoxia: part II cytotoxicity and radiosensitization applications.

Rakesh Sharma1.   

Abstract

Feasibility paper explores the cytotoxicity of nitroimidazole on tumor cells and liver cells to establish the 2'-nitroimidazole as radiosensitizer in cancer therapy and hypoxia monitoring. Hypothesis is that the presence of substituted nitro group on 2' position of imidazole ring is more enzyme sensitive and determinant of biochemical cytotoxicity as hypoxia reporter in isolated tumor cells or tumor tissues. Radiolabeling of nitroimidazole imparts tracer properties to locate the distribution (radiosensitizer) of nitroimidazole in the body. A 'theradiagnostic criteria of hypoxia' using nitroimidazole radiosensitizer is proposed based on tumor killing by enhanced tumor oxygen tension (therapeutics) and altered metabolizing enzymes (diagnostics) due to cytotoxicity of radiosensitizer. Both properties of nitroimidazole cytotoxicity and oxygen sensitivity place the nitroimidazole compounds in the class of tumor therapy and hypoxia detection. Initially nitroimidazole cytotoxicity was reported as antiparasitic drug. Now radiolabeled 2'-nitroimidazole is potential radiosensitizer in hypoxia treatment and monitoring in last two decades. Hydrophilic double radiolabel groups on imidazole ring offer multimodal imaging and active nitro- or imidazole ring in nitroimidazoles interact with intracellular metabolism in liver by biotransformation and biooxidation to cause cytotoxicity as biomarker of hypoxia. Nitroimidazole metabolizing and xenobiotic enzymes showed regulatory role to excrete out nitroimidazole from the body and reduced stay time in tissue. Nitroimidazoles showed physicochemical properties with poor tissue diffusion, less antioxidant redox potential and long retention time in tissue making them poor choice of hypoxia markers. Key of success is achieving 2'-Nitroimidazole based multimodal radiopharmaceuticals as less cytotoxic, more tumor oxygen specific multifunctional reporters of apoptosis, proliferation, and hypoxia in theradiagnostics and radiation oncology.

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Year:  2011        PMID: 22202160     DOI: 10.2174/1874471011104040379

Source DB:  PubMed          Journal:  Curr Radiopharm        ISSN: 1874-4710


  3 in total

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Journal:  Pharm Res       Date:  2016-05-26       Impact factor: 4.200

2.  Combining antiangiogenic therapy with adoptive cell immunotherapy exerts better antitumor effects in non-small cell lung cancer models.

Authors:  Shujing Shi; Rui Wang; Yitian Chen; Haizhu Song; Longbang Chen; Guichun Huang
Journal:  PLoS One       Date:  2013-06-14       Impact factor: 3.240

3.  2-Nitroimidazoles induce mitochondrial stress and ferroptosis in glioma stem cells residing in a hypoxic niche.

Authors:  Naoyoshi Koike; Ryuichi Kota; Yoshiko Naito; Noriyo Hayakawa; Tomomi Matsuura; Takako Hishiki; Nobuyuki Onishi; Junichi Fukada; Makoto Suematsu; Naoyuki Shigematsu; Hideyuki Saya; Oltea Sampetrean
Journal:  Commun Biol       Date:  2020-08-17
  3 in total

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