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Antiproliferative and apoptotic effect of Morus nigra extract on human prostate cancer cells

机译:黑桑提取物对人前列腺癌细胞的抗增殖和凋亡作用

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摘要

Background: Morus nigra L. belongs to the family Moraceae and is frequently used in traditional medicine. Numerous studies have investigated the antiproliferative effects of various extracts of different Morus species, but studies involving the in vitro cytotoxic effect of M. nigra extract are very limited. The purpose of this study was to evaluate the phenolic composition and antioxidant activity of dimethyl sulfoxide extract of M. nigra (DEM) and to investigate, for the first time, the probable cytotoxic effect in human prostate adenocarcinoma (PC-3) cells together with the mechanism involved. Methods: Total polyphenolic contents (TPC), ferric reducing antioxidant power (FRAP) and phenolic compounds of DEM were evaluated using spectrophotometric procedures and HPLC. The cytotoxic effect of DEM on PC-3 cells was revealed using the MTT assay. Mechanisms involved in the cytotoxic effect of DEM on PC-3 cells were then investigated in terms of apoptosis, mitochondrial membrane potential and cell cycle using flow cytometry, while caspase activity was investigated using luminometric analysis. Results: TPC and FRAP values were 20.7 ± 0.3 mg gallic acid equivalents and 48.8 ± 1.6 mg trolox equivalents per g sample, respectively. Ascorbic acid and chlorogenic acid were the major phenolic compounds detected at HPLC analysis. DEM arrested the cell cycle of PC-3 cells at the G1 phase, induced apoptosis via increased caspase activity and reduced mitochondrial membrane potential. Conclusions: Our results indicate that M. nigra may be a novel candidate for the development of new natural product based therapeutic agents against prostate cancer.
机译:背景:桑属桑属属于桑科,在传统医学中经常使用。许多研究已经研究了不同桑属物种的各种提取物的抗增殖作用,但是涉及黑僵菌提取物的体外细胞毒性作用的研究非常有限。这项研究的目的是评估黑质支原体(DEM)的二甲基亚砜提取物的酚类成分和抗氧化活性,并首次调查人前列腺腺癌(PC-3)细胞与涉及的机制。方法:采用分光光度法和高效液相色谱法对总多酚含量(TPC),还原铁抗氧化能力(FRAP)和DEM的酚类化合物进行了评估。使用MTT测定法揭示了DEM对PC-3细胞的细胞毒性作用。然后使用流式细胞术研究了DEM对PC-3细胞的细胞毒性作用的机制,包括细胞凋亡,线粒体膜电位和细胞周期,同时使用光度分析法研究了胱天蛋白酶的活性。结果:每克样品的TPC和FRAP值分别为20.7±0.3 mg没食子酸当量和48.8±1.6 mg trolox当量。 HPLC分析检测到主要的酚类化合物是抗坏血酸和绿原酸。 DEM阻止了PC-3细胞在G1期的细胞周期,通过增加caspase活性和降低线粒体膜电位来诱导凋亡。结论:我们的结果表明,黑质支原体可能是开发新的基于天然产物的抗前列腺癌治疗剂的新候选者。

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