Olean-12-eno[2,3-c] [1,2,5]oxadiazol-28-oic acid (OEOA) induces G1 cell cycle arrest and differentiation in human leukemia cell lines

PLoS One. 2013 May 16;8(5):e63580. doi: 10.1371/journal.pone.0063580. Print 2013.

Abstract

Oleanolic acid (3β-hydroxy-olea-12-en-28-oic acid) is a natural pentacyclic triterpenoic acid found in many fruits, herbs and medicinal plants. In the past decade, increasing evidence has suggested that oleanolic acid exhibits inhibitory activities against different types of cancer including skin cancer and colon cancer, but not leukemia. We report here that a derivative of oleanolic acid, olean-12-eno[2,3-c] [1], [2], [5]oxadiazol-28-oic acid (designated OEOA) effectively blocks the proliferation of human leukemia cells. OEOA significantly reduces cell proliferation without inducing cell death in three types of leukemia cell lines, including K562, HEL and Jurket. Moreover, exposure of K562 cells to OEOA results in G1 cell cycle arrest, with a concomitant induction of cyclin-dependent kinase inhibitor p27 and downregulation of cyclins and Cdks that are essential for cell cycle progression. Interestingly, OEOA also enhances erythroid differentiation in K562 cells through suppressing the expression of Bcr-Abl and phosphorylation of Erk1/2. These findings identify a novel chemical entity for further development as therapeutics against leukemia.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Blotting, Western
  • Cell Differentiation / drug effects
  • Cell Line, Tumor
  • Cell Survival / drug effects
  • Cyclin-Dependent Kinase Inhibitor p27 / metabolism
  • Fusion Proteins, bcr-abl / metabolism
  • G1 Phase Cell Cycle Checkpoints / drug effects*
  • Humans
  • Leukemia / metabolism
  • Oleanolic Acid / analogs & derivatives
  • Oleanolic Acid / pharmacology*
  • Phosphorylation / drug effects

Substances

  • Cyclin-Dependent Kinase Inhibitor p27
  • Oleanolic Acid
  • Fusion Proteins, bcr-abl

Grants and funding

This study is supported in part by the National Basic Research Program of China (973 Program), Shenzhen Peacock Plan, Hong Kong Research Grants Council Theme-based Research Scheme (T13-607/12R), and Innovation and Technology Fund [State Key Laboratory (ITCPT/17-9)]. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.