Investigation of discrepant proteins between two breast cancer cell lines with different metastatic abilities

Li Hong Ye*, Jia Cong You, Wei Guo, Shao Feng Xu, Lian Ying Wu, Robert Z. Qi, Xiao Dong Zhang

*Corresponding author for this work

Research output: Contribution to journalJournal Articlepeer-review

Abstract

BACKGROUND & OBJECTIVE: Metastasis associated proteins play important roles in metastasis. This study was to investigate proteins which may be involved in breast cancer cell metastasis and further explore the potential mechanisms. METHODS: LM-MCF-7 and MCF-7, two breast cancer cell lines with different metastatic potentials, derived from the same parent cell line, were used in our study. Proteomics and Western blot were applied to identify differentially expressed proteins. Wound healing assay was performed to observe the effect of survivin gene on breast cancer cell migration by transfecting pcDNA3-Sur plasmid into MCF-7 cells. RESULTS: Eight differently expressed proteins, which were correlated with cell structures, cellular metabolism, apoptosis, protein enfold or interaction, were identified. Protein expression of nm23 and p27 was relatively higher in MCF-7 cells; while the expression of survivin, Bcl-2 and myosin light chain kinase was relatively higher in LM-MCF-7 cells. Increased migration ability was observed in MCF-7 cells which were transfected with pcDNA3-Sur. CONCLUSION: Metastasis associated proteins exist in breast cancer cell lines with different metastatic abilities. Survivin is closely related to the metastasis in breast cancer cells.

Original languageEnglish
Pages (from-to)823-827
Number of pages5
Journal癌症=Chinese Journal of Cancer
Volume25
Issue number7
Publication statusPublished - Jul 2006
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Fingerprint

Dive into the research topics of 'Investigation of discrepant proteins between two breast cancer cell lines with different metastatic abilities'. Together they form a unique fingerprint.

Cite this