Altersolanol A: a selective cytotoxic anthraquinone from a Phomopsis sp

The cytotoxic compound Altersolanol A, an anthraquinone derivative was isolated from PM0409092 a fungus of Nyctanthes arbor‐tristis (family Oleaceae). It was identified as a Phomopsis sp. by DNA amplification and sequencing of the ITS region. The chemical structure of Altersolanol A was elucidated f...

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Veröffentlicht in:Letters in applied microbiology 2015-04, Vol.60 (4), p.387-391
Hauptverfasser: Mishra, P.D, Verekar, S.A, Deshmukh, S.K, Joshi, K.S, Fiebig, H.H, Kelter, G
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Sprache:eng
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Zusammenfassung:The cytotoxic compound Altersolanol A, an anthraquinone derivative was isolated from PM0409092 a fungus of Nyctanthes arbor‐tristis (family Oleaceae). It was identified as a Phomopsis sp. by DNA amplification and sequencing of the ITS region. The chemical structure of Altersolanol A was elucidated from its physicochemical properties, 2D NMR spectroscopy and other spectroscopic data. The compound has in vitro cytotoxic activity against 34 human cancer cell lines with mean IC₅₀(IC₇₀) values of 0·005 μg ml⁻¹(0·024 μg ml⁻¹) respectively. Altersolanol A, a kinase inhibitor, induces cell death by apoptosis through the cleavage by Caspase‐3 and ‐9 and by decreased anti‐apoptotic protein expression. There are several previous reports of the anticancer activity of Altersolanol A, but we report here an extensive study using 36 cell lines which gives wider spectrum of results. SIGNIFICANCE AND IMPACT OF THE STUDY: This study confirms the cytotoxic potential of Altersolanol A isolated from the endophyte Phomopsis sp. (PM0409092) of the plant Nyctanthes arbor‐tristis. The compound exhibits in vitro cytotoxicity against 34 human cancer cell lines with mean IC₅₀(IC₇₀) value of 0·005 μg ml⁻¹(0·024 μg ml⁻¹). This is an in‐depth report of Altersolanol A against a panel of 34 human cancer cell lines and extends observations from previous studies indicating that Altersolanol A can be used for the development of chemotherapeutics. Altersolanol A, a kinase inhibitor, induces cell death by apoptosis through the cleavage of Caspase‐3 and ‐9 and by decreased anti‐apoptotic protein expression.
ISSN:0266-8254
1472-765X
DOI:10.1111/lam.12384