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Current Chemical Biology

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ISSN (Print): 2212-7968
ISSN (Online): 1872-3136

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Research Article

Detection of Oncometabolite Nicotine Imine in the Nail of Oral Cancer Patients; Predicted as an Inhibitor of DNMT1

Author(s): Anwesha Deep Dutta, Ajay Kumar, Kiran Bharat Lokhande, Manmohan Mitruka, K. Venkateswara Swamy, Jayanta K. Pal, Sachin C. Sarode and Nilesh Kumar Sharma*

Volume 15, Issue 4, 2021

Page: [301 - 309] Pages: 9

DOI: 10.2174/2212796816666211223105911

Price: $65

Abstract

Background: Nicotine-metabolized product nicotine imine is suggested to play a role in metabolic changes occurring in oral cancer. There is a significant gap in the detection of oncometabolite nicotine imine in biological fluids and nails of oral cancer patients. Oncometabolites are designated as metabolites that are usually elevated in cancer cells compared to normal cells. Interestingly, a direct or indirect link is missing that establishes a role of nicotine imine in pro-cancer cellular events, including global DNA hypomethylation, a potential metabolic-epigenetic axis in oral cancer.

Methods: A novel vertical tube gel electrophoresis (VTGE) system assisted purification and liquid chromatography-high resolution mass spectrometry (LC-HRMS) based identification of nicotine imine in the nails of oral cancer patients were conducted. Further, nicotine imine was evaluated for its molecular interactions with various methyltransferases, including DNA methyltransferase 1 (DNMT1), by molecular docking and molecular dynamics (MD) simulations.

Results: Data suggested the presence of nicotine imine in the nails of oral cancer patients. Molecular docking and MD simulations revealed a specific binding affinity of nicotine imine with DNMT1. Binding with nicotine imine is within the CXCC regulatory domain of DNMT1, including key residues as ARG690, PRO574, VAL658, PRO692 and ALA695. Similar binding residues are displayed by DNMT1 inhibitor 5'-Aza-2'-deoxycytidine.

Conclusion: Nicotine imine is suggested as a predictive biomarker for oral cancer patients, and this finding is first of its kind. Molecular docking and dynamics simulation propose the role of nicotine imine as an inhibitor of DNMT1. This work supports the involvement of synergistic pro-tumor metabolic-epigenomic axis by nicotine imine that may contribute towards potential mutagenesis of normal squamous epithelium.

Keywords: Metabolites, Biomarkers, Nails, Oral cancer, Epigenetic modification, Metabolic reprogramming

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