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Native musk and synthetic musk ketone strongly induced the growth repression and the apoptosis of cancer cells

机译:天然麝香和合成麝香酮强烈诱导癌细胞的生长抑制和细胞凋亡

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Background Musk is widely used in clinical practice for its anti-cancer properties. Here, we treated various types of cancer using musk to determine which cancers are sensitive to musk treatment. We also compared effects of native musk and synthetic musk ketone in cancer cells. Furthermore, we investigated mechanisms underlying effects of musk. Methods Twenty two cancer cell lines were treated with musk. Cell proliferation and apoptosis analyses were carried out. Native musk and synthetic musk ketone were analyzed by gas chromatograph-mass spectrometer (GC-MS) assay. Differentially expressed genes were determined by microarray and quantitative real–time polymerase chain reaction. Results Native musk strongly induced the growth repression and the apoptosis in the majority of cancer cell lines in a dose-dependent manner, but distinct types of cancer showed significantly different reactions. Cancer cells which originated from epithelial cells showed higher sensitivity for musk treatment. By contrast, leukaemia and lymphoma cells were not sensitive. GC-MS analysis demonstrated that native musk contains more than 30 contents in which musk ketone is a major component; synthetic musk ketone was consistent with natural musk ketone, and the used sample of synthetic musk ketone contained only sole component. Similar to native musk, synthetic musk ketone induced the growth repression and the apoptosis of cancer cells. Additionally, numerous genes were differentially expressed in lung cancer cells after native musk treatment. These differentially expressed genes were involved in many signalling pathways. Among these pathways, apoptosis-related pathways included interleukin family, tumor necrosis factor family, and MAPK signalling pathway. Native musk and synthetic musk ketone can up-regulate IL-24 (interleukin family) and DDIT3 (MAPK signalling pathway) in lung cancer cells. Conclusions This research provided strong evidence that native musk and synthetic musk ketone can induce the growth repression and the apoptosis of cancer cells. However, the selection of sensitive cancer patient for individualized treatment is a key step in clinical application. Synthetic musk ketone can substitute for native musk to treat cancer patients. Musk might induce the growth repression and the apoptosis of lung cancer cells through up-regulating IL-24 and DDIT3 expressions.
机译:背景麝香由于其抗癌特性而在临床实践中被广泛使用。在这里,我们使用麝香治疗了各种类型的癌症,以确定哪些癌症对麝香治疗敏感。我们还比较了天然麝香和合成麝香酮在癌细胞中的作用。此外,我们调查了麝香作用的潜在机制。方法用麝香处理22个癌细胞系。进行细胞增殖和凋亡分析。天然麝香和合成麝香酮通过气相色谱-质谱仪(GC-MS)分析。通过微阵列和定量实时聚合酶链反应确定差异表达的基因。结果天然麝香以剂量依赖性方式强烈诱导大多数癌细胞系的生长抑制和凋亡,但不同类型的癌症表现出明显不同的反应。源自上皮细胞的癌细胞对麝香治疗显示出更高的敏感性。相反,白血病和淋巴瘤细胞不敏感。 GC-MS分析表明,天然麝香中含有30多种成分,其中麝香酮是主要成分。合成麝香酮与天然麝香酮一致,所用的合成麝香酮样品仅含有单一成分。与天然麝香相似,合成麝香酮可诱导癌细胞的生长抑制和凋亡。另外,天然麝香处理后,许多基因在肺癌细胞中差异表达。这些差异表达的基因参与了许多信号通路。在这些途径中,与凋亡相关的途径包括白介素家族,肿瘤坏死因子家族和MAPK信号传导途径。天然麝香和合成麝香酮可以上调肺癌细胞中的IL-24(白介素家族)和DDIT3(MAPK信号通路)。结论这项研究提供了有力的证据,证明天然麝香和合成麝香酮可以诱导癌细胞的生长抑制和细胞凋亡。但是,选择敏感的癌症患者进行个体化治疗是临床应用中的关键步骤。合成麝香酮可以替代天然麝香来治疗癌症患者。麝香可能通过上调IL-24和DDIT3的表达来诱导肺癌细胞的生长抑制和凋亡。

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