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Natural-Product-Inspired Compounds as Countermeasures against the Liver Carcinogen Aflatoxin B1.
Carter, Adam C; King, Jarrod B; Mattes, Allison O; Cai, Shengxin; Singh, Narender; Cichewicz, Robert H.
Affiliation
  • Carter AC; Natural Products Discovery Group, Institute for Natural Products Applications and Research Technologies, Department of Chemistry & Biochemistry, Stephenson Life Science Research Center , University of Oklahoma , 101 Stephenson Parkway , Norman , Oklahoma 73019 , United States.
  • King JB; Natural Products Discovery Group, Institute for Natural Products Applications and Research Technologies, Department of Chemistry & Biochemistry, Stephenson Life Science Research Center , University of Oklahoma , 101 Stephenson Parkway , Norman , Oklahoma 73019 , United States.
  • Mattes AO; Natural Products Discovery Group, Institute for Natural Products Applications and Research Technologies, Department of Chemistry & Biochemistry, Stephenson Life Science Research Center , University of Oklahoma , 101 Stephenson Parkway , Norman , Oklahoma 73019 , United States.
  • Cai S; Natural Products Discovery Group, Institute for Natural Products Applications and Research Technologies, Department of Chemistry & Biochemistry, Stephenson Life Science Research Center , University of Oklahoma , 101 Stephenson Parkway , Norman , Oklahoma 73019 , United States.
  • Singh N; CFD Research Corporation , 701 McMillian Way, Suite D , Huntsville , Alabama 35806 , United States.
  • Cichewicz RH; Natural Products Discovery Group, Institute for Natural Products Applications and Research Technologies, Department of Chemistry & Biochemistry, Stephenson Life Science Research Center , University of Oklahoma , 101 Stephenson Parkway , Norman , Oklahoma 73019 , United States.
J Nat Prod ; 82(6): 1694-1703, 2019 06 28.
Article in En | MEDLINE | ID: mdl-31136174
ABSTRACT
Aflatoxin B1 (AfB1) ranks among the most potent liver carcinogens known, and the accidental or intentional exposure of humans and livestock to this toxin remains a serious global threat. One protective measure that had been proposed is employing small-molecule therapeutics capable of mitigating the toxicity of AfB1; however, to date, these efforts have had little clinical success. To identify molecular scaffolds that reduce the toxicity of AfB1, we developed a cell-based high-throughput high-content imaging assay that enabled our team to test natural products (pure compounds, fractions, and extracts) for protection of monolayers and spheroids composed of HepG2 liver cells against AfB1. The spheroid assay showed notable potential for further development, as it afforded greater sensitivity of HepG2 cells to AfB1, which is believed to better mimic the in vivo response of hepatocytes to the toxin. One of the most bioactive compounds to arise from this investigation was alternariol-9-methyl ether (1, purified from an Alternaria sp. isolate), which inspired the synthesis and testing of several structurally related molecules. Based on these findings, it is proposed that several types of natural and synthetic polyarene molecules that have undergone oxidative functionalization (e.g., compounds containing 3-methoxyphenol moieties) are promising starting points for the development of new agents that protect against AfB1 toxicity.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Carcinogens / Aflatoxin B1 / Protective Agents / Hepatocytes / Liver / Antineoplastic Agents, Phytogenic Type of study: Prognostic_studies Limits: Humans Language: En Journal: J Nat Prod Year: 2019 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Carcinogens / Aflatoxin B1 / Protective Agents / Hepatocytes / Liver / Antineoplastic Agents, Phytogenic Type of study: Prognostic_studies Limits: Humans Language: En Journal: J Nat Prod Year: 2019 Document type: Article Affiliation country: United States