Author/Authors :
Pe?i?، نويسنده , , Milica and Bankovi?، نويسنده , , Jasna and Aljan?i?، نويسنده , , Ivana S. and Todorovi?، نويسنده , , Nina M. and Jadranin، نويسنده , , Milka and Vajs، نويسنده , , Vlatka E. and Te?evi?، نويسنده , , Vele V. and Vu?kovi?، نويسنده , , Ivan and Mom?ilovi?، نويسنده , , Miljana and Markovi?، نويسنده , , Ivanka D. and Tani?، نويسنده , , Nikola and Ru?diji?، نويسنده , , Sabera، نويسنده ,
Abstract :
Jatrophane diterpenes were shown to be inhibitors of P-glycoprotein (P-gp). There are also evidences on their microtubule-interacting activity in cancer cells. We evaluated new anti-cancer characteristics of two jatrophane type compounds from Euphorbia dendroides. For that purpose, the model system of sensitive non-small cell lung cancer cell line (NCI-H460) and its resistant counterpart (NCI-H460/R) was used. Although both jatrophanes showed inhibitory effect on cancer cell growth, they were non-toxic for peripheral blood mononuclear cells (PBMC). We examined their effects in combination with paclitaxel (PTX), a well-known mitotic spindle interacting chemotherapeutic. Jatrophanes overcome PTX resistance in concentration-dependent manner in MDR cancer cell line (NCI-H460/R). We observed that this synergistic effect is not caused merely by P-gp inhibition. In combination with PTX, jatrophanes induce cell killing and change cell cycle distribution leading to G2/M arrest. Furthermore, they exert an anti-angiogenic effect by decreasing the vascular endothelial growth factor (VEGF) secretion. The reduction of the level of mdr1 mRNA expression in sensitive cells, suggests that these compounds could not contribute to the development of resistance. In conclusion, present study provides a rational basis for the new cancer treatment approach with jatrophanes that are non-toxic to normal cells and have new favorable anti-cancer characteristics.
Keywords :
apoptosis , Jatrophane , Spurge , Multi-drug resistance (MDR) , Paclitaxel , Vascular endothelial growth factor (VEGF)