Effects of matrine on HepG2 cell proliferation and expression of tumor relevant proteins in vitro

Abstract

Matrine, one of the main active components extracted from dry roots of Sophora flavescens Ait (Leguminosae), has been reported to have anticancer effects on a number of cancer cell lines, but the anticancer mechanism of matrine remains elusive. This study shows that matrine also displays anticancer activity on human hepatocellular carcinoma (HepG2) cells. In this work, the optimal cultivation condition for HepG2 cells was determined using the combinatorial orthogonal test design [L18 (21 × 37)]. Exposure of HepG2 cells to matrine resulted in inhibition of proliferation in both a time- and dose-dependent manner, as measured by morphology observation, hematoxylin and eosin (H&E) staining, and MTT assay (p<0.05). Further immunohistochemical analyses revealed that the expression of alpha fetal protein (AFP), proliferating cell nuclear antigen (PCNA), C-myc and Bcl-2 was down-regulated significantly, but the expression of Bax was up-regulated higher than untreated cells. The results demonstrated that matrine inhibited HepG2 cells proliferation primarily via up-regulating or down-regulating expression of the tumor relevant proteins.

Keywords::

• Matrine
• HepG2 cells
• cell proliferation
• tumor relevant protein

Acknowledgements

We are sincerely grateful to Ji-Yun Yin, Si-Si Liu, Xu Xin who have contributed in many ways toward the completion of this work and Yang Jun (National University of Singapore) and Li-Jun Pu for their reviews of the manuscript.

Declaration of interest

The authors report no conflict of interests. The study was supported by the Technology Research Foundation of Education Department of HeiLongJiang Province, China (11511247).