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N-methyl-D-aspartate receptors and thymoquinone induce apoptosis and alteration in mitochondria in colorectal cancer cells

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Abstract

Colon cancer is on the rise in both men and women. In addition to traditional treatment methods, herbal treatments from complementary and alternative medicine are actively followed. Naturally derived from plants, thymoquinone (TQ) has drawn a lot of attention in the field of cancer treatment. MK-801, an N-methyl-D-aspartate agonist, is used to improve memory and plasticity, but it has also lately been explored as a potential cancer treatment. This study aimed to determine the roles of N-Methyl-D-Aspartate agonists and Thymoquinone on mitochondria and apoptosis. HT-29 cells were treated with different TQ and MK-801 concentrations. We analyzed cell viability, apoptosis, and alteration of mitochondria. Cell viability significantly decreased depending on doses of TQ and MK-801. Apoptosis and mitochondrial dysfunctions induced by low and high doses of TQ and MK-801. Our study emphasizes the need for further safety evaluation of MK-801 due to the potential toxicity risk of TQ and MK-801. Optimal and toxic doses of TQ and MK-801 were determined for the treatment of colon cancer. It should be considered as a possibility that colon cancer can be treated with TQ and MK-801.

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Authors and Affiliations

  1. Faculty of Medicine, Department of Physiology, Aydin Adnan Menderes University, Aydin, Turkey

    Ferhat Sirinyildiz

  2. Faculty of Medicine, Department of Biophysics, Lokman Hekim University, Ankara, Turkey

    Simge Unay

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  1. Ferhat Sirinyildiz
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  2. Simge Unay
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Contributions

F.S.: Conceptualization, Formal analysis, Supervision, Resources, Data Curation, Writing - Review & Editing S.U: Validation, Investigation, Methodology, Writing - Original Draft, Visualization, Project administration All authors reviewed the manuscript

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Correspondence to Simge Unay.

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Sirinyildiz, F., Unay, S. N-methyl-D-aspartate receptors and thymoquinone induce apoptosis and alteration in mitochondria in colorectal cancer cells. Med Oncol 41, 123 (2024). https://doi.org/10.1007/s12032-024-02348-y

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