1. Academic Validation
  2. Triterpenoids from Ganoderma lucidum inhibit the activation of EBV antigens as telomerase inhibitors

Triterpenoids from Ganoderma lucidum inhibit the activation of EBV antigens as telomerase inhibitors

  • Exp Ther Med. 2017 Oct;14(4):3273-3278. doi: 10.3892/etm.2017.4883.
Dong-Shu Zheng 1 Liang-Shu Chen 2
Affiliations

Affiliations

  • 1 Department of Otolaryngology Head and Neck Surgery, The First Affiliated Hospital of Xiamen University, Xiamen, Fujian 361003, P.R. China.
  • 2 Ward of Cadre Care, The First Affiliated Hospital of Xiamen University, Xiamen, Fujian 361003, P.R. China.
Abstract

Nasopharyngeal carcinoma (NPC) is a malignant disease that threatens the health of humans. To find effective agents for the inhibition of Epstein-Barr virus (EBV) Infection, which is associated with NPC, a phytochemical investigation of Ganoderma lucidum was carried out in the present study. Five triterpenoids were identified, including ganoderic acid A (compound 1), ganoderic acid B (compound 2), ganoderol B (compound 3), ganodermanontriol (compound 4), and ganodermanondiol (compound 5), on the basis of spectroscopic analysis. An inhibition of EBV antigens activation assay was implemented to elucidate the triterpenoids from G. lucidum and potentially prevent NPC. All the triterpenoids showed significant inhibitory effects on both EBV EA and CA activation at 16 nmol. At 3.2 nmol, all the compounds moderately inhibited the activation of the two antigens. The activity of Telomerase was inhibited by these triterpenoids at 10 µM. Molecular docking demonstrated that compound 1 was able to inhibit Telomerase as a ligand. In addition, the physicochemical properties of these compounds were calculated to elucidate their drug-like properties. These results provided evidence for the application of these triterpenoids and whole G. lucidum in the treatment of NPC.

Keywords

Epstein-Barr virus antigens; Ganoderma lucidum; nasopharyngeal carcinoma; physicochemical properties; telomerase inhibitor; triternepoids.

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