Cryptolepine inhibits hepatocellular carcinoma growth through inhibiting interleukin-6/STAT3 signalling

BMC Complement Med Ther. 2021 Jun 2;21(1):161. doi: 10.1186/s12906-021-03326-x.

Abstract

Background: Diverse signalling pathways are involved in carcinogenesis and one of such pathways implicated in many cancers is the interleukin 6/signal transducer and activator of transcription 3 (IL-6/STAT3) signalling pathway. Therefore, inhibition of this pathway is targeted as an anti-cancer intervention. This study aimed to establish the effect of cryptolepine, which is the main bioactive alkaloid in the medicinal plant Cryptolepis sanguinolenta, on the IL-6/STAT3 signalling pathway.

Methods: First, the effect of cryptolepine on the IL-6/STAT3 pathway in human hepatoma cells (HepG2 cells) was screened using the Cignal Finder Multi-Pathway Reporter Array. Next, to confirm the effect of cryptolepine on the IL-6/STAT3 signalling pathway, the pathway was activated using 200 ng/mL IL-6 in the presence of 0.5-2 μM cryptolepine. The levels of total STAT3, p-STAT3 and IL-23 were assessed by ELISA.

Results: Cryptolepine downregulated 12 signalling pathways including the IL-6/STAT3 signalling pathway and upregulated 17 signalling pathways. Cryptolepine, in the presence of IL-6, decreased the levels of p-STAT3 and IL-23 in a dose-dependent fashion.

Conclusion: Our results demonstrated that cryptolepine inhibits the IL-6/STAT3 signalling pathway, and therefore cryptolepine-based remedies such as Cryptolepis sanguinolenta could potentially be used as an effective immunotherapeutic agent for hepatocellular carcinoma and other cancers.

Keywords: Anti-cancer; Carcinogenesis; Cryptolepine; Hepatoma; IL-6/STAT3.

MeSH terms

  • Antineoplastic Agents, Phytogenic / pharmacology
  • Carcinoma, Hepatocellular / metabolism*
  • Cryptolepis / chemistry
  • Hep G2 Cells
  • Humans
  • Indole Alkaloids / pharmacology*
  • Interleukin-6 / metabolism*
  • Liver Neoplasms / metabolism*
  • Quinolines / pharmacology*
  • STAT3 Transcription Factor / metabolism*
  • Signal Transduction / drug effects

Substances

  • Antineoplastic Agents, Phytogenic
  • IL6 protein, human
  • Indole Alkaloids
  • Interleukin-6
  • Quinolines
  • STAT3 Transcription Factor
  • STAT3 protein, human
  • cryptolepine