Cancer drug-resistance and a look at specific proteins: Rho GDP-dissociation inhibitor 2, Y-box binding protein 1, and HSP70/90 organizing protein in proteomics clinical application

J Proteome Res. 2011 Feb 4;10(2):404-15. doi: 10.1021/pr100468w. Epub 2010 Dec 3.

Abstract

Resistance to anti-cancer drugs is a well recognized problem and very often it is responsible for failure of the cancer treatment. In this study, the proteome alterations associated with the development of acquired resistance to cyclin-depedent kinases inhibitor bohemine, a promising anti-cancer drug, were analyzed with the primary aim of identifying potential targets of resistance within the cell that could pave a way to selective elimination of specific resistant cell types. A model of parental susceptible CEM T-lymphoblastic leukemia cells and its resistant counterpart CEM-BOH was used and advanced 2-D liquid chromatography was applied to fractionate cellular proteins. Differentially expressed identified proteins were further verified using immunoblotting and immunohistochemistry. Our study has revealed that Rho GDP-dissociation inhibitor 2, Y-box binding protein 1, and the HSP70/90 organizing protein have a critical role to play in resistance to cyclin-depedent kinases inhibitor. The results indicated not only that quantitative protein changes play an important role in drug-resistance, but also that there are various other parameters such as truncation, post-translational modification(s), and subcellular localization of selected proteins. Furthermore, these proteins were validated for their roles in drug resistance using different cell lines resistant to diverse representatives of anti-cancer drugs such as vincristine and daunorubicin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents / pharmacology
  • Cell Line, Tumor
  • Chromatography, High Pressure Liquid
  • Computational Biology
  • DNA-Binding Proteins / metabolism*
  • Drug Resistance, Neoplasm*
  • Guanine Nucleotide Dissociation Inhibitors / metabolism*
  • Heat-Shock Proteins / metabolism*
  • Humans
  • Immunoblotting
  • Models, Biological
  • Nuclear Proteins / metabolism*
  • Protein Interaction Mapping
  • Proteome / analysis
  • Proteome / metabolism*
  • Purines / pharmacology
  • Spectrophotometry, Ultraviolet
  • Subcellular Fractions / metabolism
  • Tumor Suppressor Proteins / metabolism*
  • Y-Box-Binding Protein 1
  • rho-Specific Guanine Nucleotide Dissociation Inhibitors

Substances

  • Antineoplastic Agents
  • DNA-Binding Proteins
  • Guanine Nucleotide Dissociation Inhibitors
  • Heat-Shock Proteins
  • Nuclear Proteins
  • Proteome
  • Purines
  • STIP1 protein, human
  • Tumor Suppressor Proteins
  • Y-Box-Binding Protein 1
  • YBX1 protein, human
  • bohemine
  • rho-Specific Guanine Nucleotide Dissociation Inhibitors