Evaluation of Bufadienolides as the Main Antitumor Components in Cinobufacin Injection for Liver and Gastric Cancer Therapy

PLoS One. 2017 Jan 12;12(1):e0169141. doi: 10.1371/journal.pone.0169141. eCollection 2017.

Abstract

Background: Cinobufacin injection, also known as huachansu, is a preparation form of Cinobufacini made from Cinobufacin extract liquid. Despite that Cinobufacin injection is shown to shrink liver and gastric tumors, improving patient survival and life quality, the effective components in Cinobufacin remain elusive. In this study, we aim to screen antitumor components from Cinobufacin injection to elucidate the most effective antitumor components for treatment of liver and gastric cancers.

Materials and methods: High performance liquid chromatography (HPLC) and LC-MS/MS analysis were used to separate and determine the components in Cinobufacin injection. Inhibition rates of various components in Cinobufacin injection on liver and gastric cancer cells were determined with MTT assay; Hepatocellular carcinoma and gastric cancer models were used to assess the antitumor effect of the compounds in vivo.

Results: The major constituents in Cinobufacin injection include peptides, nucleic acids, tryptamines and bufotalins. MTT assay revealed that bufadienolides had the best antitumor activity, with peptides being the second most effective components. Bufadienolides showed significant inhibition rates on gastric and hepatocellular tumour growth in vivo.

Conclusion: Bufadienolides are the most effective components in Cinobufacini injection for the treatment of liver and gastric cancers. This discovery can greatly facilitate further research in improving the therapeutic effects of Cinobufacin injection, meanwhile reducing its adverse reaction.

MeSH terms

  • Amphibian Venoms / chemistry
  • Amphibian Venoms / pharmacology*
  • Animals
  • Antineoplastic Agents / chemistry
  • Antineoplastic Agents / pharmacology*
  • Bufanolides / chemistry
  • Bufanolides / pharmacology*
  • Hep G2 Cells
  • Humans
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred ICR
  • Mice, Nude
  • Neoplasms, Experimental / drug therapy*
  • Neoplasms, Experimental / metabolism
  • Neoplasms, Experimental / pathology
  • Xenograft Model Antitumor Assays

Substances

  • Amphibian Venoms
  • Antineoplastic Agents
  • Bufanolides
  • huachansu

Grants and funding

This work was supported by the Special Program for New Drug Innovation of the Ministry of Science and Technology (2013ZX09102025). Yuefei Zhang is affiliated with China Resource Sanjiu Pharmaceutical Co. Ltd., which is one of the funded entities of the grant. Yuefei Zhang and the company supplied materials used in this study, and therefore contributed to this work. The funder provided support in the form of salaries for all authors listed, but did not have any additional role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript.