Climacostol, 1,3-dihydroxy-5-[(Z)-20-nonenyl]benzene, is a natural toxin contained in the extrusomal cortical granules of the heterotrich ciliate Climacostomum virens. It is used for chemical defence against predators such as the raptorial ciliate Dileptus margaritifer and its cytotoxic activity has been assessed on several species of ciliates such as Didinium nasutum, Paramecium caudatum, and Blepharisma japonicum (Miyake et al. 2003, Europ. J. Protistol., 39:25–36). On the basis of its chemical structure, climacostol may be classified into the large group of natural compounds known as resorcinolic lipids, that show antimicrobial, antiparasitic, and antitumoral activities (Kozubek et al. 2003, Cell Moll. Biol. Lett., 6:351–355). To explore the possibility to use climacostol in medical applications, we examined the effects of chemically synthesized climacostol (Masaki et al. 2004, Tetrahedron, 60:7041–7048) on the growth and proliferation of tumoral and normal mammalian cell lines: (1) human promyelocytic leukaemia cells, HL60; (2) human squamous carcinoma cells, A431; and (3) non-tumoral cells derived from mice Leydig cells, TM3. It was observed that (1) a concentration of 10 mg/ml of climacostol exerts a strong cytotoxic activity on all cell lines used; (2) at lower concentrations of 10 ng/ml and 1 ng/ ml, the effect of climacostol is limited to the inhibition of the cell growth; and (3) the normal TM3 cells are more resistant to climacostol than the two tumoral HL60 and A431cell lines. The dose-dependent cytotoxic effects of climacostol encourage further investigation on the potential use of this ciliate toxin as an anticancer chemical.
Effects of climacostol on normal and tumoral mammalian cell lines
BRAMUCCI, Massimo;
2005-01-01
Abstract
Climacostol, 1,3-dihydroxy-5-[(Z)-20-nonenyl]benzene, is a natural toxin contained in the extrusomal cortical granules of the heterotrich ciliate Climacostomum virens. It is used for chemical defence against predators such as the raptorial ciliate Dileptus margaritifer and its cytotoxic activity has been assessed on several species of ciliates such as Didinium nasutum, Paramecium caudatum, and Blepharisma japonicum (Miyake et al. 2003, Europ. J. Protistol., 39:25–36). On the basis of its chemical structure, climacostol may be classified into the large group of natural compounds known as resorcinolic lipids, that show antimicrobial, antiparasitic, and antitumoral activities (Kozubek et al. 2003, Cell Moll. Biol. Lett., 6:351–355). To explore the possibility to use climacostol in medical applications, we examined the effects of chemically synthesized climacostol (Masaki et al. 2004, Tetrahedron, 60:7041–7048) on the growth and proliferation of tumoral and normal mammalian cell lines: (1) human promyelocytic leukaemia cells, HL60; (2) human squamous carcinoma cells, A431; and (3) non-tumoral cells derived from mice Leydig cells, TM3. It was observed that (1) a concentration of 10 mg/ml of climacostol exerts a strong cytotoxic activity on all cell lines used; (2) at lower concentrations of 10 ng/ml and 1 ng/ ml, the effect of climacostol is limited to the inhibition of the cell growth; and (3) the normal TM3 cells are more resistant to climacostol than the two tumoral HL60 and A431cell lines. The dose-dependent cytotoxic effects of climacostol encourage further investigation on the potential use of this ciliate toxin as an anticancer chemical.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
