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首页> 外文期刊>Natural Products and Bioprospecting >α-Pyrone Derivatives from a Streptomyces Strain Resensitize Tamoxifen Resistance in Breast Cancer Cells
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α-Pyrone Derivatives from a Streptomyces Strain Resensitize Tamoxifen Resistance in Breast Cancer Cells

机译:链霉菌菌株的α-吡喃酮衍生物重新敏感性乳腺癌细胞中的他莫昔芬耐药性。

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Tamoxifen resistance (TamR) is the underlying cause of treatment failure in many breast cancer patients receiving tamoxifen. In order to look for noncytotoxic natural products with the ability to reverse TamR, an extract from strain Streptomyces sp. KIB-H0495 was detected to be active. Subsequent large scale fermentation and isolation led to the isolation of four α-pyrone derivatives including two new compounds, violapyrones J (2) and K (3), and two known analogues, violapyrones B (1) and I (4). Further bioactivity assays indicated that only 1 and 3 exerted potent resensitization effects on MCF-7/TamR cells at a concentration of 1?μM. Owing to the simple structures of 1 and 3, these two compounds might have potential for further investigation as novel tamoxifen resensitization agent in breast cancer chemotherapy.Graphical AbstractOpen image in new window
机译:他莫昔芬耐药性(TamR)是许多接受他莫昔芬治疗的乳腺癌患者治疗失败的根本原因。为了寻找具有逆转TamR能力的非细胞毒性天然产物,是一种来自链霉菌属菌种的提取物。检测到KIB-H0495处于活动状态。随后的大规模发酵和分离导致了四种α-吡喃酮衍生物的分离,其中包括两种新化合物,紫罗兰酮J(2)和K(3),以及两种已知的类似物,紫罗兰酮B(1)和I(4)。进一步的生物活性测定表明,只有1和3对MCF-7 / TamR细胞具有有效的再敏化作用,浓度为1?μM。由于1和3的简单结构,这两种化合物作为新型三苯氧胺敏化剂在乳腺癌化疗中可能具有进一步研究的潜力。

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