Programmed cell death in nasopharyngeal carcinoma: Mechanisms and therapeutic targets
- PMID: 39809344
- DOI: 10.1016/j.bbcan.2025.189265
Programmed cell death in nasopharyngeal carcinoma: Mechanisms and therapeutic targets
Abstract
Programmed cell death is a type of autonomic and orderly cell death mode controlled by genes that maintain homeostasis and growth. Tumor is a typical manifestation of an imbalance in environmental homeostasis in the human body. Currently, several tumor treatments are designed to trigger the death of tumor cells. Nasopharyngeal carcinoma is one of the most common malignant tumors in China. It displays obvious regional and ethnic differences in its incidence, being typically high in the south and low in the north of China. Nasopharyngeal carcinoma is currently considered to be a polygenic inherited disease and is often mediated by the interaction between multiple genes or between genes and the environment. Apoptosis has long been considered the key to tumor treatment, while other cell death pathways have often been overlooked. The current study provides an overview of the relationship among apoptosis, autophagy, pyroptosis, necroptosis, ferroptosis, and nasopharyngeal carcinoma, and the regulatory pathways of nasopharyngeal carcinoma based on five cell death modes were synthesized from the view of molecule. We hope this review will help explore additional, novel programmed cell death targets for the treatment of nasopharyngeal carcinoma and thus promote in-depth research.
Keywords: Clinical transformation; Mechanisms; Nasopharyngeal carcinoma; Programmed cell death; Therapeutic targets.
Copyright © 2025 Elsevier B.V. All rights reserved.
Conflict of interest statement
Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
Similar articles
-
BIX-01294-enhanced chemosensitivity in nasopharyngeal carcinoma depends on autophagy-induced pyroptosis.Acta Biochim Biophys Sin (Shanghai). 2020 Oct 19;52(10):1131-1139. doi: 10.1093/abbs/gmaa097. Acta Biochim Biophys Sin (Shanghai). 2020. PMID: 33085742
-
Jervine exhibits anticancer effects on nasopharyngeal carcinoma through promoting autophagic apoptosis via the blockage of Hedgehog signaling.Biomed Pharmacother. 2020 Dec;132:110898. doi: 10.1016/j.biopha.2020.110898. Epub 2020 Oct 28. Biomed Pharmacother. 2020. PMID: 33113432
-
MicroRNA-205 targets HER3 and suppresses the growth, chemosensitivity and metastasis of human nasopharyngeal carcinoma cells.J BUON. 2020 Jan-Feb;25(1):350-356. J BUON. 2020. PMID: 32277654
-
Selected Flavonols Targeting Cell Death Pathways in Cancer Therapy: The Latest Achievements in Research on Apoptosis, Autophagy, Necroptosis, Pyroptosis, Ferroptosis, and Cuproptosis.Nutrients. 2024 Apr 18;16(8):1201. doi: 10.3390/nu16081201. Nutrients. 2024. PMID: 38674891 Free PMC article. Review.
-
The Role of PTEN in Nasopharyngeal Carcinoma.Front Biosci (Landmark Ed). 2024 May 10;29(5):179. doi: 10.31083/j.fbl2905179. Front Biosci (Landmark Ed). 2024. PMID: 38812313 Review.
Cited by
-
Emerging roles of tsRNAs in programmed cell death and disease therapeutics: challenges, opportunities, and future directions.Noncoding RNA Res. 2025 Jul 11;15:65-73. doi: 10.1016/j.ncrna.2025.07.003. eCollection 2025 Dec. Noncoding RNA Res. 2025. PMID: 40809958 Free PMC article. Review.
-
RAD51 modulates in nasopharyngeal carcinoma cells by regulating Caspase-8-mediated pyroptosis.Discov Oncol. 2025 Jul 12;16(1):1320. doi: 10.1007/s12672-025-03100-2. Discov Oncol. 2025. PMID: 40650821 Free PMC article.
-
Ursolic acid induces apoptosis in nasopharyngeal carcinoma cells through the P53 signaling pathway: a network pharmacology and experimental validation study.Med Oncol. 2025 May 1;42(6):189. doi: 10.1007/s12032-025-02749-7. Med Oncol. 2025. PMID: 40310511
References
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources