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Determining the Optimal Inhibitory Frequency for Cancerous Cells Using Tumor Treating Fields TTFields
Published on: May 4, 2017
Inhibitory effects of 3-bromopyruvate in human nasopharyngeal carcinoma cells
Xue Zou1, Mengxiao Zhang1, Yiming Sun1
1Faculty of Pharmacy, Bengbu Medical College, Bengbu, Anhui 233004, P.R. China.
Abstract:
Tumor cells depend on aerobic glycolysis for adenosine triphosphate (ATP) production, which is therefore targeted by therapeutic agents. The compound 3-bromopyruvate (3-BrPA), a strong alkylating agent and hexokinase inhibitor, inhibits tumor cell glycolysis and the production of ATP, causing apoptosis. 3-BrPA induces apoptosis of nasopharyngeal carcinoma (NPC) cell lines HNE1 and CNE-2Z, which may be related to its molecular mechanisms. In the present study, we investigated the effects of 3-BrPA on the viability, reactive oxygen species (ROS), apoptosis and other types of programmed cell death in NPC cells in vitro and in vivo. PI staining showed significant apoptosis in NPC cells accompanied by the overproduction of ROS and downregulation of mitochondrial membrane potential (MMP, ΔΨm) by 3-BrPA. However, the ROS scavenger N-acetyl-L-cysteine (NAC) significantly reduced 3-BrPA-induced apoptosis by decreasing ROS and facilitating the recovery of MMP. We elucidated the molecular mechanisms underlying 3-BrPA activity and found that it caused mitochondrial dysfunction and ROS production, leading to necroptosis of NPC cells. We investigated the effects of the caspase inhibitor z-VAD-fmk, which inhibits apoptosis but promotes death domain receptor (DR)-induced NPC cell necrosis. Necrostatin-1 (Nec-1) inhibits necroptosis, apparently via a DR signaling pathway and thus abrogates the effects of z-VAD‑fmk. In addition, we demonstrated the effective attenuation of 3-BrPA-induced necrotic cell death by Nec-1. Finally, animal studies proved that 3-BrPA exhibited significant antitumor activity in nude mice. The present study is the first demonstration of 3-BrPA-induced non-apoptotic necroptosis and ROS generation in NPC cells and provides potential strategies for developing agents against apoptosis‑resistant cancers.
Insights
3-bromopyruvate (3-BrPA) triggers necroptosis, a form of programmed cell death, in nasopharyngeal carcinoma cells by increasing reactive oxygen species (ROS) and impairing mitochondrial function. This compound shows significant antitumor activity in vivo.
Area of Science:
- Oncology
- Cell Biology
- Biochemistry
Background:
- Tumor cells rely on aerobic glycolysis for ATP production, making it a therapeutic target.
- 3-bromopyruvate (3-BrPA) is a hexokinase inhibitor that halts glycolysis and ATP production, inducing apoptosis in cancer cells.
- Previous studies indicated 3-BrPA induces apoptosis in nasopharyngeal carcinoma (NPC) cells.
Purpose of the Study:
- To investigate the effects of 3-BrPA on NPC cell viability, reactive oxygen species (ROS) production, and programmed cell death pathways.
- To elucidate the molecular mechanisms underlying 3-BrPA's action in NPC cells.
- To evaluate the in vivo antitumor efficacy of 3-BrPA.
Main Methods:
- In vitro studies on NPC cell lines (HNE1, CNE-2Z) assessing viability, ROS levels, mitochondrial membrane potential (MMP), and apoptosis.
- Treatment with 3-BrPA, ROS scavenger N-acetyl-L-cysteine (NAC), caspase inhibitor z-VAD-fmk, and necroptosis inhibitor Necrostatin-1 (Nec-1).
- In vivo antitumor activity assessment in nude mouse models.
Main Results:
- 3-BrPA induced significant apoptosis, ROS overproduction, and decreased MMP in NPC cells.
- NAC treatment reduced 3-BrPA-induced apoptosis, ROS, and restored MMP.
- 3-BrPA triggered necroptosis, not solely apoptosis, mediated by mitochondrial dysfunction and ROS, inhibited by Nec-1.
- 3-BrPA demonstrated significant antitumor activity in vivo.
Conclusions:
- 3-BrPA induces non-apoptotic necroptosis and ROS generation in NPC cells via mitochondrial dysfunction.
- The findings reveal novel molecular mechanisms of 3-BrPA action.
- 3-BrPA presents a potential therapeutic strategy for apoptosis-resistant cancers.

