Protein-Bound Polysaccharide from Corbicula fluminea Inhibits Cell Growth in MCF-7 and MDA-MB-231 Human Breast Cancer Cells

PLoS One. 2016 Dec 13;11(12):e0167889. doi: 10.1371/journal.pone.0167889. eCollection 2016.

Abstract

A novel protein-bound polysaccharide, CFPS-1, isolated from Corbicula fluminea, is composed predominantly of mannose (Man) and glucose (Glc) in a molar ratio of 3.1:12.7. The polysaccharide, with an average molecular weight of about 283 kDa, also contains 10.8% protein. Atomic force microscopy, high-performance liquid chromatography, Fourier transform infrared spectroscopy, gas chromatography/mass spectrometry, and nuclear magnetic resonance spectroscopy analyses revealed that CFPS-1 has a backbone of 1,6-linked and 1,4,6-linked-α-D-Glc, which is terminated with a 1-linked-α-D-Man residue at the O-4 position of 1,4,6-linked-α-D-Glc, in a molar ratio of 3:1:1. Preliminary in vitro bioactivity tests revealed that CFPS-1 effectively and dose-dependently inhibits human breast cancer MCF-7 and MDA-MB-231 cell growth, with an IC50 of 243 ± 6.79 and 1142 ± 14.84 μg/mL, respectively. In MCF-7, CFPS-1 produced a significant up-regulation of p53, p21, Bax and cleaved caspase-7 and down-regulation of Cdk4, cyclin D1, Bcl-2 and caspase-7. These effects resulted in cell cycle blockade at the S-phase and apoptosis induction. In contrast, in MDA-MB-231, with limited degree of change in cell cycle distribution, CFPS-1 increases the proportion of cells in apoptotic sub-G1 phase executed by down-regulation of Bcl-2 and caspase-7 and up-regulation of Bax and cleaved caspase-7. This study extends our understanding of the anticancer mechanism of C. fluminea protein-bound polysaccharide.

MeSH terms

  • Animals
  • Antineoplastic Agents / chemistry
  • Antineoplastic Agents / pharmacology*
  • Apoptosis
  • Caspase 7 / genetics
  • Caspase 7 / metabolism
  • Cell Proliferation / drug effects*
  • Corbicula / chemistry*
  • Cyclin D1 / genetics
  • Cyclin D1 / metabolism
  • Cyclin-Dependent Kinase 4 / genetics
  • Cyclin-Dependent Kinase 4 / metabolism
  • Glucose / analysis
  • Humans
  • MCF-7 Cells
  • Mannose / analysis
  • Polysaccharides / chemistry
  • Polysaccharides / pharmacology*
  • Proto-Oncogene Proteins c-bcl-2 / genetics
  • Proto-Oncogene Proteins c-bcl-2 / metabolism
  • Tumor Suppressor Protein p53 / genetics
  • Tumor Suppressor Protein p53 / metabolism

Substances

  • Antineoplastic Agents
  • Polysaccharides
  • Proto-Oncogene Proteins c-bcl-2
  • Tumor Suppressor Protein p53
  • Cyclin D1
  • CDK4 protein, human
  • Cyclin-Dependent Kinase 4
  • Caspase 7
  • Glucose
  • Mannose

Grants and funding

This research was sponsored by the National Natural Science Foundation of China (NO. 31371872), http://fund.sciencenet.cn/index.php/item/view/207237/, the Public Projects of Zhejiang Province (NO. 2015C32017), http://www.zjkjt.gov.cn/news/node01/detail0101/2015/0101_61846.htm, the Program of Health and Medicine Science in Zhejiang Province (NO. 2015RCA003), http://www.doc88.com/p-6572488490711.html, Major Science and Technology Special Projects of Zhejiang, China (NO. 2013C03045-1) and Zhejiang Provincial Program for the Cultivation of High-level Innovative Health Talents, http://www.decmin.com/zj_view.asp?id=919. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.