The quinolone derivative CHM-1 inhibits murine WEHI-3 leukemia in BALB/c mice in vivo

Leuk Lymphoma. 2010 Nov;51(11):2098-102. doi: 10.3109/10428194.2010.517279. Epub 2010 Sep 17.

Abstract

CHM-1 [2-(2-fluorophenyl)-6,7-methylenedioxyquinolin-4-one] is a quinolone derivative that has been reported to induce apoptosis and inhibit invasion of cancer cells. However, there is no available information to address the effects of CHM-1 on leukemia cells in vivo. Therefore, the present study examined the effects of CHM-1 using a mouse model of leukemia. We established leukemia in mice by injecting WEHI-3 cells into BALB/c mice. Mice were then treated with or without CHM-1 (5 and 10 mg/kg). CHM-1 promoted the total survival rate of leukemic mice and these effects were dose-dependent. CHM-1 increased body weight and decreased spleen weight, but did not affect liver weight. The levels of cell markers Mac-3 and CD11b were reduced by CHM-1, indicating that the differentiation of macrophage precursor cells was inhibited. Levels of CD3 and CD19 were induced by CHM-1, suggesting that the differentiation of precursors of T and B cells was promoted in PBMC. Results of the present study indicate that CHM-1 has an inhibitory effect on leukemia induced in mice in vivo and warrants further study as to the mechanisms and effects in other types of cancer.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antineoplastic Agents / pharmacology
  • Antineoplastic Agents / therapeutic use
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Dioxoles / pharmacology*
  • Dioxoles / therapeutic use
  • Dose-Response Relationship, Drug
  • Down-Regulation / drug effects
  • Drug Evaluation, Preclinical
  • Leukemia / mortality
  • Leukemia / pathology*
  • Leukemia / prevention & control*
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Models, Biological
  • Neoplasm Transplantation
  • Quinolones / pharmacology*
  • Quinolones / therapeutic use
  • Survival Analysis

Substances

  • 2'-fluoro-6,7-methylenedioxy-2-phenyl-4-quinolone
  • Antineoplastic Agents
  • Dioxoles
  • Quinolones