Lantana camara Induces Apoptosis by Bcl-2 Family and Caspases Activation

Pathol Oncol Res. 2015 Apr;21(2):325-31. doi: 10.1007/s12253-014-9824-4. Epub 2014 Aug 22.

Abstract

Breast cancer is one of the most common cancers worldwide, and the second most fatal cancer in women after lung cancer. Because there are instances of cancer resistance to existing therapies, studies focused on the identification of novel therapeutic drugs are very important. In this study, we identified a natural anticancer agent from Lantana camara, a flowering plant species of the genus Verbena. The extract obtained from the L. camara exhibited cell death properties in the human breast cancer cell line, MCF-7. We found that the apoptosis induced by treatment with the L. camara extract was regulated by the Bcl-2 family. Bid and Bax was increased and Bcl-2 was decreased by L. camara extract. L. camara extract modulated cleavage of caspase-8, and caspase-9, as well as poly (ADP-ribose) polymerase (PARP). Our results support the potential use of the L. camara extract as an anti-breast cancer drug.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenocarcinoma / enzymology
  • Adenocarcinoma / pathology
  • Antineoplastic Agents / pharmacology
  • Apoptosis / drug effects*
  • Apoptosis / physiology
  • BH3 Interacting Domain Death Agonist Protein / drug effects
  • BH3 Interacting Domain Death Agonist Protein / metabolism
  • Breast Neoplasms / enzymology
  • Breast Neoplasms / pathology*
  • Caspase 8 / drug effects*
  • Caspase 8 / metabolism
  • Caspase 9 / drug effects*
  • Caspase 9 / metabolism
  • Cell Cycle / drug effects
  • Cell Cycle / physiology
  • Cell Line, Tumor
  • Female
  • Humans
  • In Vitro Techniques
  • Lantana*
  • Plant Extracts / pharmacology*
  • Poly(ADP-ribose) Polymerases / drug effects
  • Poly(ADP-ribose) Polymerases / metabolism
  • Proto-Oncogene Proteins c-bcl-2 / drug effects*
  • Proto-Oncogene Proteins c-bcl-2 / metabolism
  • Signal Transduction / drug effects
  • Signal Transduction / physiology
  • bcl-2-Associated X Protein / drug effects
  • bcl-2-Associated X Protein / metabolism

Substances

  • Antineoplastic Agents
  • BH3 Interacting Domain Death Agonist Protein
  • BID protein, human
  • Plant Extracts
  • Proto-Oncogene Proteins c-bcl-2
  • bcl-2-Associated X Protein
  • Poly(ADP-ribose) Polymerases
  • Caspase 8
  • Caspase 9