Discovery of small molecules targeting GRP78 for antiangiogenic and anticancer therapyv

Yixue Qiao, Charlotte Dsouza, Abigail Ann Matthews, Yan Jin, Wan He, Jian Bao, Faqin Jiang, Ritu Chandna, Ruowen Ge, Lei Fu*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

12 Citations (Scopus)

Abstract

Glucose Regulated Protein 78 kDa (GRP78) is an attractive antiangiogenic and anticancer target for its selective accumulation on the surface of cancer cells and cancer endothelial cells rather than normal cells. In this study, we identified a novel series of small molecules that binds to GRP78, exhibiting potent antiangiogenic and anticancer activities without affecting normal cells. Among these, FL5,2-(4-((4-acetamidophenoxy)methyl)phenyl)-N-isobutylbenzofuran-3-carboxamide, was superior to others due to its strong binding affinity to GRP78 (an increase in the Tm > 2 °C stabilising the GRP78 protein) and potent antiangiogenic and anticancer activities against human umbilical vein endothelial cells (HUVEC) (EC50 = 1.514 μM) and human renal cancer cells (786-O) (50% cell death at 10 μM). Furthermore, FL5 displayed no cytotoxic activity towards mouse fibroblast cells (Swiss-3T3), which do not harbour cell surface GRP78 under normal condition. FL5 was less detrimental to ATPase activity, which is essential for normal cells, as seen in the virtual docking studies. This study reports the discovery of novel small molecules targeting GRP78 with potent antiangiogenic and anticancer activities and less toxicity to normal cells, which provides prototype candidates for novel paths for cancer therapy.

Original languageEnglish
Article number112228
JournalEuropean Journal of Medicinal Chemistry
Volume193
DOIs
Publication statusPublished - 1 May 2020
Externally publishedYes

Keywords

  • Antiangiogenesis
  • Anticancer
  • Cell-surface GRP78
  • Glucose regulated protein 78 kDa
  • Small molecule ligands

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