Curcumol inhibits EBV-positive Nasopharyngeal carcinoma migration and invasion by targeting nucleolin

[Display omitted] Metastasis is a major cause of recurrence and death in patients with EBV-positive Nasopharyngeal carcinoma (NPC). Previous reports documented that curcumol has both anti-cancer and anti-viral effects, but there is little literature systematically addressing the mechanism of curcumo...

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Veröffentlicht in:Biochemical pharmacology 2021-10, Vol.192, p.114742-114742, Article 114742
Hauptverfasser: Guan, Xiao, Yu, Dan, HuangFu, Mengjie, Huang, Zhiyi, Dou, Tong, Liu, Yisa, Zhou, Luwei, Li, Xumei, Wang, Lin, Liu, Haiping, Wang, Juan, Chen, Xu
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Sprache:eng
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Zusammenfassung:[Display omitted] Metastasis is a major cause of recurrence and death in patients with EBV-positive Nasopharyngeal carcinoma (NPC). Previous reports documented that curcumol has both anti-cancer and anti-viral effects, but there is little literature systematically addressing the mechanism of curcumol in EBV-positive tumors. Previously we found that nucelolin (NCL) is a target protein of curcumol in CNE2 cells, an EBV-negative NPC, and in this experiment, we reported a critical role for NCL in promoting migration and invasion of C666-1 cells, an EBV-positive NPC, and found that the expression of NCL determined the level of curcumol's efficacy. Mechanistically, NCL interacted with Epstein-Barr Virus Nuclear Antigen 1 (EBNA1) to activate VEGFA/VEGFR1/PI3K/AKT signaling pathway, which in turn promoted NPC cell invasion and metastasis. Moreover, further study showed that the differential expression of NCL and curcumol intervention only had a regulatory effect on the nuclear accumulation of VEGFR1, which strengthened the anti-cancer effect of curcumol mediated through NCL. Our findings indicated that curcumol exerted anti EBV-positive NPC invasion and metastasis by downregulating EBNA1 and inhibiting VEGFA/VEGFR1/PI3K/AKT signaling by targeting NCL, which provides a novel pharmacological basis for curcumol's clinical use in treating patients with EBV-positive NPC
ISSN:0006-2952
1873-2968
DOI:10.1016/j.bcp.2021.114742