Pharmacological Ascorbate Elicits Anti-Cancer Activities against Non-Small Cell Lung Cancer through Hydrogen-Peroxide-Induced-DNA-Damage

Non-small cell lung cancer (NSCLC) poses a significant global health burden with unsatisfactory survival rates, despite advancements in diagnostic and therapeutic modalities. Novel therapeutic approaches are urgently required to improve patient outcomes. Pharmacological ascorbate (P-AscH<sup>−...

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Main Authors: Kittipong Sanookpan (Author), Naphat Chantaravisoot (Author), Nuttiya Kalpongnukul (Author), Chatchapon Chuenjit (Author), Onsurang Wattanathamsan (Author), Sara Shoaib (Author), Pithi Chanvorachote (Author), Visarut Buranasudja (Author)
Format: Book
Published: MDPI AG, 2023-09-01T00:00:00Z.
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Summary:Non-small cell lung cancer (NSCLC) poses a significant global health burden with unsatisfactory survival rates, despite advancements in diagnostic and therapeutic modalities. Novel therapeutic approaches are urgently required to improve patient outcomes. Pharmacological ascorbate (P-AscH<sup>−</sup>; ascorbate at millimolar concentration in plasma) emerged as a potential candidate for cancer therapy for recent decades. In this present study, we explore the anti-cancer effects of P-AscH<sup>−</sup> on NSCLC and elucidate its underlying mechanisms. P-AscH<sup>−</sup> treatment induces formation of cellular oxidative distress; disrupts cellular bioenergetics; and leads to induction of apoptotic cell death and ultimately reduction in clonogenic survival. Remarkably, DNA and DNA damage response machineries are identified as vulnerable targets for P-AscH<sup>−</sup> in NSCLC therapy. Treatments with P-AscH<sup>−</sup> increase the formation of DNA damage and replication stress markers while inducing mislocalization of DNA repair machineries. The cytotoxic and genotoxic effects of P-AscH<sup>−</sup> on NSCLC were reversed by co-treatment with catalase, highlighting the roles of extracellular hydrogen peroxide in anti-cancer activities of P-AscH<sup>−</sup>. The data from this current research advance our understanding of P-AscH<sup>−</sup> in cancer treatment and support its potential clinical use as a therapeutic option for NSCLC therapy.
Item Description:10.3390/antiox12091775
2076-3921