Celastrol induces vincristine multidrug resistance oral cancer cell apoptosis by targeting JNK1/2 signaling pathway

Phytomedicine. 2019 Feb 15:54:1-8. doi: 10.1016/j.phymed.2018.09.181. Epub 2018 Sep 17.

Abstract

Background: Oral cancers are one of the most aggressive malignancies, with high mortality rates globally. Patients with these cancers are treated using combination therapies including surgery, chemotherapy, and radiotherapy.

Hypothesis/purpose: Traditional Chinese medicines and other herbal medicines have been used to treat various diseases in Asia. Celastrol is a pentacyclic triterpenoid isolated from the Chinese herbal medicine Trypterygium wilfordii, which has therapeutic potential in multiple diseases. The present study was to determine the effect of celastrol on vincristine-resistant cancer cell line and to illuminate the mechanism of celastrol-induced cell apoptosis.

Study design: Celastrol was added to vincristine-resistant cancer cell and immunoreactive proteins were detected.

Methods and results: Our study demonstrated that celastrol leads to apoptosis of head and neck cancer cells through mitochondria- and Fas-mediated pathways. However, whether this herbal medicine exhibits beneficial effects on vincristine-resistant oral cancer patients remains uncertain. Therefore, our study examined the apoptotic effect exerted by celastrol and the mechanism by this drug acts on a vincristine-resistant cancer cell line. The present study demonstrated that celastrol triggered apoptotic cell death by inducing cell cycle arrest at the G2/M phase via the intrinsic and extrinsic pathways (increased cleaved caspase-3, caspase-8, caspase-9, and PARP). Increased expression of tBid also indicated the presence of crosstalk between the two pathways. Celastrol mediated cell apoptosis through the downregulation of the expression of Bcl-2, not Bcl-xL. Moreover, JNK1/2 signaling was the main pathway of celastrol-induced apoptosis.

Conclusion: Celastrol could become a useful agent for treating oral cancers with MDR.

Keywords: Apoptosis; Celastrol; Multidrug resistance; Oral cancer; Vincristine.

MeSH terms

  • Antineoplastic Agents, Phytogenic / pharmacology*
  • Apoptosis / drug effects
  • Cell Cycle Checkpoints / drug effects
  • Cell Line, Tumor
  • Drug Resistance, Multiple / drug effects
  • Drug Resistance, Neoplasm / drug effects*
  • Drugs, Chinese Herbal / chemistry
  • Humans
  • MAP Kinase Signaling System / drug effects
  • Mouth Neoplasms / drug therapy*
  • Mouth Neoplasms / metabolism
  • Mouth Neoplasms / pathology
  • Pentacyclic Triterpenes
  • Proto-Oncogene Proteins c-bcl-2 / metabolism
  • Signal Transduction / drug effects
  • Triterpenes / pharmacology*
  • Vincristine / pharmacology

Substances

  • Antineoplastic Agents, Phytogenic
  • BCL2 protein, human
  • Drugs, Chinese Herbal
  • Pentacyclic Triterpenes
  • Proto-Oncogene Proteins c-bcl-2
  • Triterpenes
  • Vincristine
  • celastrol