Published June 2013 | Version v1
Journal article

Self-assembled monolayers with different chemical group substrates for the study of MCF-7 breast cancer cell line behavior

  • 1. Bio-X Center, School of Life Science and Technology, Harbin Institute of Technology, Harbin 150080 (China)
  • 2. State Key Laboratory of Cancer Biology and Xijing Hospital of Digestive Diseases, The Fourth Military Medical University, Number 15, Xi'an 710032 (China)
  • 3. State Key Laboratory of New Ceramics and Fine Processing, School of Materials Science and Engineering, Tsinghua University, Beijing 100084 (China)
  • 4. Department of Mechanical Engineering, University of Saskatchewan, Saskatoon (Canada)

Description

The interactions between cancer cells and the extracellular matrix (ECM) are important with respect to a number of cell behavoirs, yet remain unclear. In this study, self-assembled monolayers with different terminal chemical groups (hydroxyl (-OH), carboxyl (-COOH), animo (-NH2), mercapto (-SH), and methyl (-CH3)) were employed as substrates for the culture of MCF-7 cells to examine effects on cell behavior. Cell spreading was investigated by scanning electron microscopy, tallin expression by immunofluorescence, proliferation rate by counting cell numbers, cell cycle by flow cytometry, metabolism by high-performance liquid chromatography and cell migration by live cell imaging. Annexin V-FITC (fluorescein isothiocyanate) and JC-1 assays were performed to determine cell apoptosis and mitochondrial membrane potential, respectively. Our results demonstrate the varied behaviors of MCF-7 cells in response to different chemical groups. Specifically, NH2 and COOH terminal functional groups promote proliferation, the production of lactic acid and mobility of MCF-7 cells; SH and OH terminal groups enhance the expression and distribution of tallin but result in weak cell proliferation, metabolism, spreading and mobility. These results are meaningful for uncovering the interactions between the ECM and cancer cells; they are potentially useful for designing novel cancer treatment strategies. (paper)

Availability note (English)

Available from http://dx.doi.org/10.1088/1748-6041/8/3/035008

Additional details

Identifiers

Publishing Information

Journal Title
Biomedical Materials (Bristol. Online)
Journal Volume
8
Journal Issue
3
Journal Page Range
[9 p.]
ISSN
1748-605X