Ophiobolin A, a sesterterpenoid produced by plant pathogenic fungi, was purified from the culture extract of Drechslera gigantea and tested for its growth-inhibitory activity in both plant and mammalian cells. Ophiobolin A induced cell death in Nicotiana tabacum L. cv. Bright Yellow 2 (TBY-2) cells at concentrations ≥10 µM, with the TBY-2 cells showing typical features of apoptosis-like cell death. At a concentration of 5 µM, ophiobolin A did not affect plant cell viability but prevented cell proliferation. When tested on eight cancer cell lines, concentrations <1 µM of ophiobolin A inhibited growth by 50% after 3 days of culture irrespective of their multidrug resistance (MDR) phenotypes and their resistance levels to pro-apoptotic stimuli. It is, thus, unlikely that ophiobolin A exerts these in vitro growth-inhibitory effects in cancer cells by activating pro-apoptotic processes. Highly proliferative human keratinocytes appeared more sensitive to the growth-inhibitory effects of ophiobolin A than slowly proliferating ones. Ophiobolin A also displayed significant antitumor activity at the level of mouse survival when assayed at 10 mg/kg in the B16F10 mouse melanoma model with lung pseudometastases. Ophiobolin A could, thus, represent a novel scaffold to combat cancer types that display various levels of resistance to pro-apoptotic stimuli and/or various MDR phenotypes. - See more at: http://www.spandidos-publications.com/10.3892/ijo.2013.1979#sthash.xAVfklqx.dpuf

Ophiobolin A, a sesterterpenoid fungal phytotoxin, displays higher in vitro growth-inhibitory effects in mammalian than in plant cells and displays in vivo antitumor activity / M., B., E., N.U., Andolfi, A., S., C., N., W., P., H., B., L., F., A., C., D., Cimmino, A., J., D., P., V.A., M. C., Z., M., V., Y., P., W., B., Evidente, A., L., D.G., R., K., V., L.. - In: INTERNATIONAL JOURNAL OF ONCOLOGY. - ISSN 1019-6439. - 43:2(2013), pp. 575-585. [10.3892/ijo.2013.1979]

Ophiobolin A, a sesterterpenoid fungal phytotoxin, displays higher in vitro growth-inhibitory effects in mammalian than in plant cells and displays in vivo antitumor activity.

ANDOLFI, ANNA;CIMMINO, ALESSIO;EVIDENTE, ANTONIO;
2013

Abstract

Ophiobolin A, a sesterterpenoid produced by plant pathogenic fungi, was purified from the culture extract of Drechslera gigantea and tested for its growth-inhibitory activity in both plant and mammalian cells. Ophiobolin A induced cell death in Nicotiana tabacum L. cv. Bright Yellow 2 (TBY-2) cells at concentrations ≥10 µM, with the TBY-2 cells showing typical features of apoptosis-like cell death. At a concentration of 5 µM, ophiobolin A did not affect plant cell viability but prevented cell proliferation. When tested on eight cancer cell lines, concentrations <1 µM of ophiobolin A inhibited growth by 50% after 3 days of culture irrespective of their multidrug resistance (MDR) phenotypes and their resistance levels to pro-apoptotic stimuli. It is, thus, unlikely that ophiobolin A exerts these in vitro growth-inhibitory effects in cancer cells by activating pro-apoptotic processes. Highly proliferative human keratinocytes appeared more sensitive to the growth-inhibitory effects of ophiobolin A than slowly proliferating ones. Ophiobolin A also displayed significant antitumor activity at the level of mouse survival when assayed at 10 mg/kg in the B16F10 mouse melanoma model with lung pseudometastases. Ophiobolin A could, thus, represent a novel scaffold to combat cancer types that display various levels of resistance to pro-apoptotic stimuli and/or various MDR phenotypes. - See more at: http://www.spandidos-publications.com/10.3892/ijo.2013.1979#sthash.xAVfklqx.dpuf
2013
Ophiobolin A, a sesterterpenoid fungal phytotoxin, displays higher in vitro growth-inhibitory effects in mammalian than in plant cells and displays in vivo antitumor activity / M., B., E., N.U., Andolfi, A., S., C., N., W., P., H., B., L., F., A., C., D., Cimmino, A., J., D., P., V.A., M. C., Z., M., V., Y., P., W., B., Evidente, A., L., D.G., R., K., V., L.. - In: INTERNATIONAL JOURNAL OF ONCOLOGY. - ISSN 1019-6439. - 43:2(2013), pp. 575-585. [10.3892/ijo.2013.1979]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/552508
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