Two novel silver(I) phenanthroline derivative complexes induce G2/M phase cycle arrest and apoptosis of MDA‐MB‐231 cancer cells by multiple mechanisms

Author:

Niu Zong‐ling1ORCID,Wu Tian‐Tian1ORCID,Wu Yuan‐yuan1ORCID,Zhou Si‐Han1ORCID,Li Zhe2ORCID,Guo Ji‐Chao1ORCID,Zhou Shu‐Min1ORCID,Deng Shi‐Hui1ORCID,Xu Jing‐Yuan2ORCID,Xie Ming‐Jin1ORCID

Affiliation:

1. School of Chemical Science and Technology Yunnan University Kunming China

2. Department of Chemical Biology and Tianjin Key Laboratory on Technologies Enabling Development of Clinical Therapeutics and Diagnostics (Theranostics), School of Pharmacy Tianjin Medical University Tianjin China

Abstract

Two novel silver(I) phenanthroline derivative complexes (P‐235 and P‐239) have been synthesized and characterized by IR, HPLC‐MS, and 1HNMR. The cytotoxicity of two complexes exhibited significant cytotoxicity against human breast cancer (MDA‐MB‐231) cell line (IC50 = 0.48 ± 0.01 and 0.12 ± 0.01 μM) and less toxicity than cisplatin by MTT assays. Furthermore, anticancer mechanistic studies showed that P‐235 and P‐239 induced G2/M phase cell cycle arrest to inhibit the growth of MDA‐MB‐231 cells. Flow cytometry analysis showed that MDA‐MB‐231 cells could be significantly induced to undergo apoptosis by P‐235 and P‐239. And P‐235‐ and P‐239‐induced apoptosis was linked with reactive oxygen species (ROS) production. Further study revealed that P‐235 and P‐239 cause mitochondrial membrane potential depolarization and destroy mitochondrial membrane potential.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Inorganic Chemistry,General Chemistry

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