High Throughput Screening for Colorectal Cancer Specific Compounds

Comb Chem High Throughput Screen. 2016;19(3):180-8. doi: 10.2174/1386207319666160202120928.

Abstract

The development of new anti-cancer therapeutic agents is necessary to improve antitumor efficacy and reduce toxicities. Here we report using a systematic anticancer drug screening approach we developed previously, to concurrently screen colon and glioma cancer cell lines for 2000 compounds with known bioactivity and 1920 compounds with unknown activity. The hits specific to each tumor cell line were then selected, and further tested with the same cells transfected with EGFP (Enhanced Green Fluorescent Protein) alone. By comparing the percentage of signal reduction from the same cells transfected with the sensor-conjugated reporter system; hits preferably causing apoptosis were identified. Among the known lead compounds, many cardiac glycosides used as cardiotonic drugs were found to effectively and specifically kill colon cancer cells, while statins (hypolipidemic agents) used as cholesterol lowering drugs were relatively more effective in killing glioma cells.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Antineoplastic Agents / chemical synthesis
  • Antineoplastic Agents / chemistry
  • Antineoplastic Agents / pharmacology*
  • Apoptosis / drug effects
  • Cardiac Glycosides / chemical synthesis
  • Cardiac Glycosides / chemistry
  • Cardiac Glycosides / pharmacology*
  • Cardiotonic Agents / chemical synthesis
  • Cardiotonic Agents / chemistry
  • Cardiotonic Agents / pharmacology
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Colorectal Neoplasms / drug therapy*
  • Colorectal Neoplasms / pathology
  • Dose-Response Relationship, Drug
  • Drug Screening Assays, Antitumor*
  • Glioma / drug therapy*
  • Glioma / pathology
  • High-Throughput Screening Assays*
  • Humans
  • Hypolipidemic Agents / chemical synthesis
  • Hypolipidemic Agents / chemistry
  • Hypolipidemic Agents / pharmacology
  • Structure-Activity Relationship

Substances

  • Antineoplastic Agents
  • Cardiac Glycosides
  • Cardiotonic Agents
  • Hypolipidemic Agents