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Updated: Jun 19, 2025

Preparation of Naringenin Solution for In Vivo Application
Published on: August 10, 2021
Naringin Induces ROS-Stimulated G1 Cell-Cycle Arrest and Apoptosis in Nasopharyngeal Carcinoma Cells
Chan-Hung Chen1,2, Ni Tien3, Chun-Hsu Yao4
1Department of Medical Laboratory Science and Biotechnology, China Medical University, Taichung, Taiwan.
Abstract:
Naringin, a bioflavonoid compound from grapefruit or citrus, exerts anticancer activities on cervical, thyroid, colon, brain, liver, lung, thyroid, and breast cancers. The present investigation addressed exploring the anticancer effects of naringin on nasopharyngeal carcinoma (NPC) cells. Naringin exhibits a cytotoxic effect on NPC-TW 039 and NPC-TW 076 cells with IC50 372/328 and 394/307 μM for 24 or 48 h, respectively, while causing little toxicity toward normal gingival epithelial (SG) cells (>500/500 μM). We established that naringin triggered G1 arrest is achieved by suppressing cyclin D1, cyclin A, and CDK2, and upregulating p21 protein in NPC cells. Exposure of NPC cells to naringin caused a series of events leading to apoptosis including morphology change (cell shrinkage and membrane blebbing) and chromatin condensation. Annexin V and PI staining indicated that naringin treatment promotes necrosis and late apoptosis in NPC cells. DiOC6 staining showed a decline in the mitochondrial membrane potential by naringin treatment, which was followed with cytochrome c release, Apaf-1/caspase-9/-3 activation, PARP cleavage, and EndoG expression in NPC cells. Naringin upregulated proapoptotic Bax and decreased antiapoptotic Bcl-xL expression, and dysregulated Bax/Bcl-xL ratio in NPC cells. Notably, naringin enhanced death receptor-related t-Bid expression. Furthermore, an increased Ca2+ release by naringin treatment which instigated endoplasmic reticulum stress-associated apoptosis through increased IRE1, ATF-6, GRP78, GADD153, and caspase-12 expression in NPC cells. In addition, naringin triggers ROS production, and inhibition of naringin-induced ROS generation by antioxidant N-acetylcysteine resulted in the prevention of G1 arrest and apoptosis in NPC cells. Naringin-induced ROS-mediated G1 arrest and mitochondrial-, death receptor-, and endoplasmic reticulum stress-mediated apoptosis may be a promising strategy for treating NPC.
Insights
Naringin, a citrus bioflavonoid, shows anticancer effects against nasopharyngeal carcinoma (NPC) cells by inducing cell cycle arrest and apoptosis. This compound offers a promising strategy for NPC treatment with minimal toxicity to normal cells.
Area of Science:
- Biochemistry
- Molecular Biology
- Oncology
Background:
- Naringin, a citrus bioflavonoid, demonstrates anticancer properties against various cancer types.
- Nasopharyngeal carcinoma (NPC) remains a significant health concern, necessitating novel therapeutic strategies.
Purpose of the Study:
- To investigate the anticancer effects of naringin on nasopharyngeal carcinoma (NPC) cells.
- To elucidate the molecular mechanisms underlying naringin's cytotoxic and apoptotic effects in NPC.
Main Methods:
- Cell viability assays (IC50 determination) on NPC and normal gingival epithelial cells.
- Flow cytometry for cell cycle analysis (G1 arrest) and apoptosis/necrosis detection (Annexin V/PI, DiOC6 staining).
- Western blotting to assess protein expression involved in cell cycle regulation, apoptosis pathways (mitochondrial, death receptor, ER stress), and ROS production.
Main Results:
- Naringin exhibited dose- and time-dependent cytotoxicity against NPC cells with low toxicity to normal cells.
- Naringin induced G1 cell cycle arrest by modulating cyclin/CDK regulators and p21.
- Naringin triggered apoptosis via intrinsic (mitochondrial), extrinsic (death receptor), and ER stress pathways, evidenced by caspase activation, PARP cleavage, and altered Bcl-2 family proteins.
- Naringin treatment increased intracellular reactive oxygen species (ROS) production, which was crucial for G1 arrest and apoptosis.
Conclusions:
- Naringin effectively inhibits NPC cell proliferation and induces apoptosis through multiple molecular pathways.
- Naringin-mediated ROS production plays a critical role in its anticancer effects on NPC.
- Naringin represents a potential therapeutic agent for nasopharyngeal carcinoma treatment.
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