Apoptotic cell death of stomach cancer lines (AGS) induced by Co-NTB complex through cellular organelles and DNA damage

Given that stomach cancer is the fourth leading cause of cancer-related death, there is a need to develop new drugs. Among various methods, metal-based coordination compounds are considered as an efficient strategy against this type of cancer. Similarly, the benzimidazole moiety plays a crucial role in biology; thus, various benzimidazole-based compounds have been found to be active as potential anticancer drugs and are currently used in clinical trials. In this study, we explored the benzimidazole-based cobalt(ii) complex as an anticancer agent against AGS stomach cancer cell lines. Interestingly, the MTT assay of the Co-NTB complex shows a lower IC<sub>50</sub> value of 4.25 μg mL<sup>-1</sup> compared to cisplatin, which has an IC<sub>50</sub> of 7.5 μg mL<sup>-1</sup> against AGS cell lines. Light microscopy and Hoechst/propidium iodide dye staining clearly indicate that the complex damages DNA, leading to cell death through an apoptotic pathway. The apoptotic cell death pathway was further complemented by Lysotracker and Mitotracker staining, as well as transmission electron microscopy (TEM) imaging. Overall, the Co-NTB complex acts as an effective anticancer agent against AGS stomach cancer cell lines, with apoptotic cell death induced by targeting cellular organelles and DNA.

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Publication Details

Journal
RSC Advances
Published
2025-01-01
DOI
https://doi.org/10.1039/d4ra06377e
Citations
5
Primary Topic
Chemotherapy-induced organ toxicity mitigation
Type
article
Field-Weighted Citation Impact
7.36

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article

Apoptotic cell death of stomach cancer lines (AGS) induced by Co-NTB complex through cellular organelles and DNA damage

Daewon Sohn, Mohamed Farouk Elsadek, Sivaraman Somasundaram, Mani Balamurugan et al.
5 citations
RSC Advances
Chemotherapy-induced organ toxicity mitigation
7.36
article

Apoptotic cell death of stomach cancer lines (AGS) induced by Co-NTB complex through cellular organelles and DNA damage

Daewon Sohn, Mohamed Farouk Elsadek, Sivaraman Somasundaram, Mani Balamurugan, Saeedah Musaed Almutairi, Haribalan Perumalsamy, Sumitha Purushothaman, Ivan Mijakovic̀, Shadi Rahimi, Sri Renukadevi Balusamy
article en
5 citations

Abstract

Given that stomach cancer is the fourth leading cause of cancer-related death, there is a need to develop new drugs. Among various methods, metal-based coordination compounds are considered as an efficient strategy against this type of cancer. Similarly, the benzimidazole moiety plays a crucial role in biology; thus, various benzimidazole-based compounds have been found to be active as potential anticancer drugs and are currently used in clinical trials. In this study, we explored the benzimidazole-based cobalt(ii) complex as an anticancer agent against AGS stomach cancer cell lines. Interestingly, the MTT assay of the Co-NTB complex shows a lower IC<sub>50</sub> value of 4.25 μg mL<sup>-1</sup> compared to cisplatin, which has an IC<sub>50</sub> of 7.5 μg mL<sup>-1</sup> against AGS cell lines. Light microscopy and Hoechst/propidium iodide dye staining clearly indicate that the complex damages DNA, leading to cell death through an apoptotic pathway. The apoptotic cell death pathway was further complemented by Lysotracker and Mitotracker staining, as well as transmission electron microscopy (TEM) imaging. Overall, the Co-NTB complex acts as an effective anticancer agent against AGS stomach cancer cell lines, with apoptotic cell death induced by targeting cellular organelles and DNA.

RSC AdvancesVol. 15(2)
Seoul National University (KR), Novo Nordisk Foundation (DK), King Saud University (SA), Sejong University (KR), Biotronik (India) (IN), Hanyang University (KR), Chalmers University of Technology (SE), Saveetha University (IN), Technical University of Denmark (DK)
National Research Foundation, King Saud University, National Research Foundation of Korea
Good health and well-being
Openalex Percentile: Top 3%
Chemotherapy-induced organ toxicity mitigation
7.36
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