Modification of DNA structure by reactive nitrogen species as a result of 2-methoxyestradiol–induced neuronal nitric oxide synthase uncoupling in metastatic osteosarcoma cells

Giampaolo Barone, Fabrizio Lo Celso, Giosue' Lo Bosco, Michal Szkatula, Alicja Kuban-Jankowska, Magdalena Gorska-Ponikowska, Agata Ploska, Michal Wozniak, Monika Gorzynik-Debicka, Dagmara Jacewicz, Narcyz Knap, Giosuè Lo Bosco, Lawrence Wawrzyniec Dobrucki, Leszek Kalinowski, Aleksandra M Dabrowska, Lech Chmurzynski, Michal Wozniak

Research output: Contribution to journalArticle

Abstract

2-methoxyestradiol (2-ME) is a physiological anticancer compound, metabolite of 17β-estradiol. Previously, our group evidenced that from mechanistic point of view one of anticancer mechanisms of action of 2-ME is specific induction and nuclear hijacking of neuronal nitric oxide synthase (nNOS), resulting in local generation of nitro-oxidative stress and finally, cancer cell death. The current study aims to establish the substantial mechanism of generation of reactive nitrogen species by 2-ME. We further achieved to identify the specific reactive nitrogen species involved in DNA-damaging mechanism of 2-ME. The study was performed using metastatic osteosarcoma 143B cells. We detected the release of biologically active (free) nitric oxide (•NO) with concurrent measurements of peroxynitrite (ONOO−) in real time in a single cell of 143B cell line by using •NO/ONOO− sensitive microsensors after stimulation with calcium ionophore. Detection of nitrogen dioxide (•NO2) and determination of chemical rate constants were carried out by a stopped-flow technique. The affinity of reactive nitrogen species toward the guanine base of DNA was evaluated by density functional theory calculations. Expression and localization of nuclear factor NF-kB was determined using imaging cytometry, while cell viability assay was evaluated by MTT assay. Herein, we presented that 2-ME triggers pro-apoptotic signalling cascade by increasing cellular reactive nitrogen species overproduction – a result of enzymatic uncoupling of increased nNOS protein levels. In particular, we proved that ONOO− and •NO2 directly formed from peroxynitrous acid (ONOOH) and/or by auto-oxidation of •NO, are inducers of DNA damage in anticancer mechanism of 2-ME. Specifically, the affinity of reactive nitrogen species toward the guanine base of DNA, evaluated by density functional theory calculations, decreased in the order: ONOOH > ONOO− > •NO2 > •NO. Therefore, we propose to consider the specific inducers of nNOS as an effective tool in the field of chemotherapy.
Original languageEnglish
Pages (from-to)1-10
Number of pages10
JournalRedox Biology
Volume32
Publication statusPublished - 2020

All Science Journal Classification (ASJC) codes

  • Organic Chemistry
  • Clinical Biochemistry

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    Barone, G., Lo Celso, F., Lo Bosco, G., Szkatula, M., Kuban-Jankowska, A., Gorska-Ponikowska, M., Ploska, A., Wozniak, M., Gorzynik-Debicka, M., Jacewicz, D., Knap, N., Lo Bosco, G., Dobrucki, L. W., Kalinowski, L., Dabrowska, A. M., Chmurzynski, L., & Wozniak, M. (2020). Modification of DNA structure by reactive nitrogen species as a result of 2-methoxyestradiol–induced neuronal nitric oxide synthase uncoupling in metastatic osteosarcoma cells. Redox Biology, 32, 1-10.