CAY10585 (LW 6)

LW6 inhibits HIF-1α expression induced by hypoxia. It promotes apoptosis preferentially in hypoxic cells. Treatment with LW6 presents no additive effect on cell cycle arrest. LW6 induces ROS formation through the depolarization of MMP in hypoxic cells. Although LW6 increases mitochondrial ROS production, the combination with hypoxia induces a marked increase in ROS production and this high level is maintained up until 24 h. LW6 is also a specific inhibitor of MDH2. As MDH2 is known to serve a significant role in the citric acid cycle at the mitochondrial membrane, LW6 indirectly reduces the activity of the mitochondrial respiratory chain through the inhibition of MDH2^[1].In contrast to BCRP, LW6 has no inhibition effect on the functional activity and gene expression of P-gp^[2]. LW6 also down-regulates BCRP expression at concentrations of 0.1-10 μM. Furthermore, cells become more susceptible to the cytotoxicity of anticancer drugs in the presence of LW6^[3].

LW6 exerts marked anti-tumor efficacy in vivo and causes reductions in HIF-1α expression levels in mice carrying xeno-grafts of HCT116 cells^[1]. LW6 improves the cytotoxicity and bioavailability of anticancer drugs translocated by BCRP^[3].

• Cell lines

  A549 cells

• Concentrations

  5-100 μM

• Incubation Time

  24 h

• Method

  Cells are incubated in 96-well ELISA Plates with 100 μl culture medium at 2×10⁵ cells/ml with or without LW6 for 24 h. Cell viability is assessed by the dimethyl thiazolcarboxy-methoxyphenylsulfophenyltetrazolium (MTS) assay. The absorbance is measured at 490 and 620 nm using a microplate reader. For the trypan blue dye. exclusion test, cells are stained by phosphate-buffered saline (PBS) containing 0.1% trypan blue. Cell viability is assessed by counting the number of unstained cells.

• Animal Models

  Male Sprague-Dawley rats

• Dosages

  10 mg/kg

• Administration

  p.o.