4.7 Article

Biological evaluation of mitochondria targeting small molecules as potent anticancer drugs

期刊

BIOORGANIC CHEMISTRY
卷 114, 期 -, 页码 -

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.bioorg.2021.105055

关键词

Mitochondria; Mitochondria-targeting compounds; ROS; Mitochondrial membrane potential; Apoptosis; Mitochondrial chemotherapy

资金

  1. Medical-Engineering Joint Fund of Shanghai Jiao Tong University [YG2017MS29, ZH2018ZDB07]
  2. Agilent research Award [4608]
  3. Chinese government scholarship (CSC)

向作者/读者索取更多资源

This study investigated the inhibitory activity of mitochondria targeting small molecules on human cervical cancer cells and demonstrated their therapeutic potential. In both in vitro and in vivo experiments, these molecules showed promising inhibitory effects on cancer cells, promoting potential apoptosis and necrosis.
Cancer therapy targets specific metabolic pathways or a single gene. This may result in low therapeutic effects due to drug selectivity and drug resistance. Recent studies revealed that the mitochondrial membrane potential and transmembrane permeability of cancerous mitochondria are differed from normal mitochondria. Thus, chemotherapy targeting cancerous mitochondria could be an innovative and competent strategy for cancer therapy. Previously, our work with a novel group of mitochondria targeting small molecules presented promising inhibitory capability toward various cancer cell lines and suppressed adenosine triphosphate (ATP) generation. Therefore, it is critical to understand the anticancer effect and targeting mechanism of these small molecules. This study investigated the inhibitory activity of mitochondria targeting small molecules with human cervical cancer cells - HeLa to further explore their therapeutic potential. HeLa cells were exposed to 10 mu M of syn-thesized compounds and presented elevation in intracellular reactive oxygen species (ROS) level, impaired mitochondrial membrane potential and upregulation of apoptosis as well as necrosis. In vivo, HeLa cell tumor-bearing BALB/c nude mice were treated with mitochondria targeting small molecules for 12 days consecu-tively. Throughout this chemotherapy study, no deleterious side effects nor the appearance of toxicity was observed. Furthermore, mitochondria targeting small molecules treated groups exhibited significant down-regulation with both tumor volume and tumor weight compared to the Doxorubicin (DOX) treated group. Thus, inhibition of mitochondrial ATP synthesis, activation of intracellular ROS production, down-regulation of mitochondrial membrane potential and upregulation of apoptosis and necrosis rates are the indications of cancer therapy. In this work, we examined the anticancer capability of four mitochondria targeting small molecules in vitro and in vivo, and demonstrated a novel therapeutic approach in cancer therapy with tremendous potential.

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