Matrine inhibited proliferation and increased apoptosis in human breast cancer MCF-7 cells via upregulation of Bax and downregulation of Bcl-2

Int J Clin Exp Pathol. 2015 Nov 1;8(11):14793-9. eCollection 2015.

Abstract

Purpose: The aim of the present study was to investigate the effects of matrine on proliferation and apoptosis in human breast cancer MCF-7 cells and its relevant molecular mechanisms.

Methods: Breast carcinoma cell line MCF-7 was cultured with series concentrations of Matrine in vitro. The proliferation and apoptosis of MCF-7 cells were investigated by 3-(4, 5-dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium bromide (MTT) assay, flow cytometry, and Mitochondrial membrane potential (MMP) measurements. The expression levels of Bax and Bcl-2 proteins were detected by Annexin V/propidium iodide coupled staining. The morphological changes of MCF-7 cell were examined.

Results: The inhibition rates of MCF-7 cells were 6.01%-37.01%, 7.56%-53.92%, and 10.86%-70.23% for 24, 48, and 72 hours after Matrine treatment, respectively. The proliferation of MCF-7 cells was significantly inhibited by Matrine administration, with a time and dose dependent manner. The rates apoptotic cells was between 4.17±0.25% and 19.63±0.17% in 0.25-2.0 mg/ml Matrine groups, which had significant increased compare with the control groups (1.10±0.08%, P<0.05). Meanwhile, increased Bax expression, but decreased Bcl-2 expression was observed in MCF-7 cell line. MMP were significantly decreased by Matrine treatment.

Conclusions: Matrine significantly inhibited the growth and induced apoptosis in breast carcinoma MCF-7 cells, which is related to Bax, Bcl-2 signaling and MMP.

Keywords: Bax; Bcl-2; Matrine; apoptosis; breast cancer; mitochondrial; proliferation.

MeSH terms

  • Alkaloids / pharmacology*
  • Antineoplastic Agents, Phytogenic / pharmacology*
  • Apoptosis / drug effects*
  • Breast Neoplasms / metabolism*
  • Breast Neoplasms / pathology
  • Cell Proliferation / drug effects*
  • Down-Regulation
  • Female
  • Flow Cytometry
  • Humans
  • MCF-7 Cells
  • Matrines
  • Proto-Oncogene Proteins c-bcl-2 / biosynthesis
  • Quinolizines / pharmacology*
  • Up-Regulation
  • bcl-2-Associated X Protein / biosynthesis

Substances

  • Alkaloids
  • Antineoplastic Agents, Phytogenic
  • BCL2 protein, human
  • Proto-Oncogene Proteins c-bcl-2
  • Quinolizines
  • bcl-2-Associated X Protein
  • Matrines