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白皮杉醇在实验性乳腺癌中的化学预防和治疗功效:体内和体外机制分析。

Chemopreventive and Therapeutic Efficacy of L. Bark in Experimental Breast Carcinoma: Mechanistic In Vivo and In Vitro Analyses.

机构信息

Department of Medical Biology, Jessenius Faculty of Medicine, Comenius University in Bratislava, 03601 Martin, Slovakia.

Division of Oncology, Biomedical Center Martin, Comenius University in Bratislava, Jessenius Faculty of Medicine, 036 01 Martin, Slovakia.

出版信息

Molecules. 2020 Mar 19;25(6):1399. doi: 10.3390/molecules25061399.

Abstract

Comprehensive oncology research suggests an important role of phytochemicals or whole plant foods in the modulation of signaling pathways associated with anticancer action. The goal of this study is to assess the anticancer activities of L. using rat, mouse, and cell line breast carcinoma models. (as bark powder) was administered in the diet at two concentrations of 0.1% (w/w) and 1% (w/w) during the whole experiment in chemically induced rat mammary carcinomas and a syngeneic 4T1 mouse model. After autopsy, histopathological and molecular evaluations of mammary gland tumors in rodents were carried out. Moreover, in vitro analyses using MCF-7 and MDA-MB-231 cells were performed. The dominant metabolites present in the tested essential oil (with relative content over 1%) were cinnamaldehyde, cinnamaldehyde dimethyl acetal, cinnamyl acetate, eugenol, linalool, eucalyptol, limonene, o-cymol, and α-terpineol. The natural mixture of mentioned molecules demonstrated significant anticancer effects in our study. In the mouse model, at a higher dose (1%) significantly decreased tumor volume by 44% when compared to controls. In addition, treated tumors showed a significant dose-dependent decrease in mitotic activity index by 29% (0.1%) and 45.5% (1%) in comparison with the control group. In rats, in both doses significantly reduced the tumor incidence by 15.5% and non-significantly suppressed tumor frequency by more than 30% when compared to controls. An evaluation of the mechanism of anticancer action using valid oncological markers showed several positive changes after treatment with . Histopathological analysis of treated rat tumor specimens showed a significant decrease in the ratio of high-/low-grade carcinomas compared to controls. In treated rat carcinomas, we found caspase-3 and Bax expression increase. On the other hand, we observed a decrease in Bcl-2, Ki67, VEGF, and CD24 expressions and MDA levels. Assessment of epigenetic changes in rat tumor cells in vivo showed a significant decrease in lysine methylation status of H3K4m3 and H3K9m3 in the high-dose treated group, a dose-dependent increase in H4K16ac levels (H4K20m3 was not changed), down-regulations of miR21 and miR155 in low-dose cinnamon groups (miR22 and miR34a were not modulated), and significant reduction of the methylation status of two out of five gene promoters- and (, , promoters were not changed). In vitro study confirmed results of animal studies, in that the essential oil of displayed significant anticancer efficacy in MCF-7 and MDA-MB-231 cells (using MTS, BrdU, cell cycle, annexin V/PI, caspase-3/7, Bcl-2, PARP, and mitochondrial membrane potential analyses). As a conclusion, L. showed chemopreventive and therapeutic activities in animal breast carcinoma models that were also significantly confirmed by mechanistic evaluations in vitro and in vivo.

摘要

综合肿瘤学研究表明,植物化学物质或全植物食物在与抗癌作用相关的信号通路调节中具有重要作用。本研究的目的是评估 L. 使用大鼠、小鼠和乳腺癌细胞系模型的抗癌活性。(作为树皮粉)在化学诱导的大鼠乳腺癌和同源 4T1 小鼠模型中以 0.1%(w/w)和 1%(w/w)的两种浓度添加到饮食中。在安乐死后,对啮齿动物的乳腺肿瘤进行了组织病理学和分子评估。此外,还进行了 MCF-7 和 MDA-MB-231 细胞的体外分析。在所测试的精油中存在的主要代谢物(相对含量超过 1%)为肉桂醛、肉桂醛二甲缩醛、肉桂基乙酸酯、丁香酚、芳樟醇、桉油醇、柠檬烯、o-丁香酚和α-松油醇。在所研究的天然混合物中,提到的分子表现出显著的抗癌作用。在小鼠模型中,高剂量(1%)组与对照组相比,肿瘤体积显著减少 44%。此外,与对照组相比,处理后的肿瘤有丝分裂活性指数显著降低 29%(0.1%)和 45.5%(1%)。在大鼠中,两种剂量均显著降低肿瘤发生率 15.5%,而非显著降低肿瘤发生率超过 30%。使用有效的肿瘤标志物评估抗癌作用的机制表明,用 处理后发生了几种阳性变化。用处理的大鼠肿瘤标本的组织病理学分析显示,与对照组相比,高低级癌的比例显著降低。在治疗的大鼠癌中,我们发现 caspase-3 和 Bax 的表达增加。另一方面,我们观察到 Bcl-2、Ki67、VEGF 和 CD24 表达和 MDA 水平降低。体内大鼠肿瘤细胞中表观遗传变化的评估显示,高剂量处理组 H3K4m3 和 H3K9m3 的赖氨酸甲基化状态显著降低,H4K16ac 水平呈剂量依赖性增加(H4K20m3 没有改变),低剂量肉桂组中的 miR21 和 miR155 下调(miR22 和 miR34a 没有调节),两个基因启动子中的两个的甲基化状态显著降低- 和 -(,- 启动子没有改变)。体外研究证实了动物研究的结果,即 的精油在 MCF-7 和 MDA-MB-231 细胞中显示出显著的抗癌功效(使用 MTS、BrdU、细胞周期、 Annexin V/PI、caspase-3/7、Bcl-2、PARP 和线粒体膜电位分析)。总之,L. 在动物乳腺癌模型中表现出化学预防和治疗活性,这也通过体外和体内的机制评估得到了显著证实。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28cc/7144360/de631c1d1c6f/molecules-25-01399-g001.jpg

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