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Naringin Induces ROS-Stimulated G1 Cell-Cycle Arrest and Apoptosis in Nasopharyngeal Carcinoma Cells.
Chen, Chan-Hung; Tien, Ni; Yao, Chun-Hsu; Chen, Siang-Jyun; Bau, Da-Tian; Pandey, Sudhir; Yang, Hsin-Ling; Hseu, You-Cheng; Chen, Shih-Shun; Lin, Meng-Liang.
Afiliación
  • Chen CH; Department of Medical Laboratory Science and Biotechnology, China Medical University, Taichung, Taiwan.
  • Tien N; Graduate Institute of Biomedical Science, China Medical University, Taichung, Taiwan.
  • Yao CH; Department of Laboratory Medicine, China Medical University Hospital, Taichung, Taiwan.
  • Chen SJ; Department of Biomedical Images and Radiological Science, China Medical University, Taichung, Taiwan.
  • Bau DT; Department of Nutrition, College of Health Care, China Medical University, Taichung, Taiwan.
  • Pandey S; Graduate Institute of Biomedical Science, China Medical University, Taichung, Taiwan.
  • Yang HL; Department of Cosmeceutics, College of Pharmacy, China Medical University, Taichung, Taiwan.
  • Hseu YC; Department of Nutrition, College of Health Care, China Medical University, Taichung, Taiwan.
  • Chen SS; Department of Cosmeceutics, College of Pharmacy, China Medical University, Taichung, Taiwan.
  • Lin ML; Department of Medical Laboratory Science and Biotechnology, College of Medical and Health Science, Asia University, Taichung, Taiwan.
Environ Toxicol ; 2024 Jul 26.
Article en En | MEDLINE | ID: mdl-39056589
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.
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Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Environ Toxicol Asunto de la revista: SAUDE AMBIENTAL / TOXICOLOGIA Año: 2024 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Environ Toxicol Asunto de la revista: SAUDE AMBIENTAL / TOXICOLOGIA Año: 2024 Tipo del documento: Article