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The First Multimodal Anticancer Manganese(II) Complex of an Asymmetric Anthrahydrazone Triggers Apoptosis, Autophagy
Rui-Xue Liu1, Dong-Mei Li1,2, Ru-Yi Luo1
1School of Chemistry and Pharmaceutical Sciences, Key Laboratory for Chemistry and Molecular Engineering of Medicinal Resources (Ministry of Education of China), Guangxi Key Laboratory of Chemistry and Molecular Engineering of Medicinal Resources, University Engineering Research Center of Authentic Medicinal Resource Chemistry, Guangxi Normal University, Guangxi, Guilin 541004, China.
Abstract:
A new nonsymmetric anthrahydrazone ligand (AAIH) was designed and synthesized, affording novel manganese(II) and cobalt(II) complexes, AAIH-Mn and AAIH-Co. Both complexes crystallized in the same centrosymmetric dinuclear coordination mode, however, AAIH-Mn exhibited much higher in vitro cytotoxicity (IC50 = 1.64 μM against MGC-803 cells) than AAIH-Co (IC50 = 10.05 μM) and AAIH (IC50 = 18.82 μM), signifying the importance of the Mn(II) center. Furthermore, AAIH-Mn exerted anticancer activity via multiple pathways: S-phase cell cycle arrest, cell apoptosis, autophagy and notably, the emerging process of ferroptosis. AAIH-Mn also effectively inhibited 56% of tumor growth in vivo on MGC-803 xenografts at 16 mg/kg, without causing obvious toxicity. Low toxicity was further supported by zebrafish models, along with its anti-inflammatory activity and low cardiotoxicity. As the first Mn(II) complex inducing ferroptosis, AAIH-Mn provides a valuable example of a low-toxicity metal center to generate highly cytotoxic nonplatinum anticancer complex.
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