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一种新型抗癌剂的发现:在体外和体内人肺腺癌A549细胞中靶向拓扑异构酶I和II以及端粒酶活性——肉桂成分香芹醛

Discovery of a Novel Anti-Cancer Agent Targeting Both Topoisomerase I & II as Well as Telomerase Activities in Human Lung Adenocarcinoma A549 Cells In Vitro and In Vivo: Cinnamomum verum Component Cuminaldehyde.

作者信息

Chen Ta-Wei, Tsai Kuen-Daw, Yang Shu-Mei, Wong Ho-Yiu, Liu Yi-Heng, Cherng Jonathan, Chou Kuo-Shen, Wang Yang-Tz, Cuizon Janise, Cherng Jaw-Ming

机构信息

Department of Internal Medicine, Saint Mary's Hospital Luodong, Yilan 26546, Taiwan, ROC.

出版信息

Curr Cancer Drug Targets. 2016;16(9):796-806. doi: 10.2174/1568009616666160426125526.

Abstract

Cinnamomum verum is used to make the spice cinnamon and has been used for more than 5000 years by both of the two most ancient forms of medicine in the words: Ayurveda and traditional Chinese herbal medicines for various applications such as adenopathy, rheumatism, dermatosis, dyspepsia, stroke, tumors, elephantiasis, trichomonas, yeast, and virus infections. We evaluated the anticancer effect of cuminaldehyde (CuA), a constituent of the bark of the plant, and its underlying molecular biomarkers associated with carcinogenesis in human lung adenocarcinoma A549 cells. The results show that cuminaldehyde suppressed proliferation and induced apoptosis as indicated by mitochondrial membrane potential loss, activation of caspase 3 and 9, increase in annexin V+PI+ cells, and morphological characteristics of apoptosis, including blebbing of plasma membrane, nuclear condensation, fragmentation, apoptotic body formation, and comet with elevated tail intensity and moment. In addition, cuminaldehyde also induced lysosomal vacuolation with increased volume of acidic compartments (VAC), suppressions of both topoisomerase I & II as well as telomerase activities in a dose-dependent manner. Further study reveals the growth-inhibitory effect of cuminaldehyde was also evident in a nude mice model. Taken together, the data suggest that the growth-inhibitory effect of cuminaldehyde against A549 cells is accompanied by downregulations of proliferative control involving apoptosis, both topoisomerase I & II as well as telomerase activities, together with an upregulation of lysosomal vacuolation and VAC. Similar effects (including all of the above-mentioned effects) were found in other cell lines, including human lung squamous cell carcinoma NCI-H520 and colorectal adenocarcinoma COLO 205 (results not shown). Our data suggest that cuminaldehyde could be a potential agent for anticancer therapy.

摘要

锡兰肉桂用于制作香料肉桂,在世界上两种最古老的医学——阿育吠陀医学和传统中草药中已有5000多年的使用历史,用于多种病症,如腺病、风湿病、皮肤病、消化不良、中风、肿瘤、象皮病、滴虫病、酵母菌感染和病毒感染等。我们评估了该植物树皮成分香芹醛(CuA)对人肺腺癌A549细胞的抗癌作用及其与致癌作用相关的潜在分子生物标志物。结果表明,香芹醛抑制细胞增殖并诱导凋亡,表现为线粒体膜电位丧失、半胱天冬酶3和9激活、膜联蛋白V+PI+细胞增加以及凋亡的形态学特征,包括质膜起泡、核浓缩、碎片化、凋亡小体形成以及彗星尾强度和矩增加。此外,香芹醛还诱导溶酶体空泡化,酸性区室(VAC)体积增加,以剂量依赖方式抑制拓扑异构酶I和II以及端粒酶活性。进一步研究表明,香芹醛在裸鼠模型中也具有明显的生长抑制作用。综上所述,数据表明香芹醛对A549细胞的生长抑制作用伴随着涉及凋亡、拓扑异构酶I和II以及端粒酶活性的增殖控制下调,同时溶酶体空泡化和VAC上调。在其他细胞系中也发现了类似的作用(包括上述所有作用),包括人肺鳞状细胞癌NCI-H520和结肠腺癌COLO 205(结果未显示)。我们的数据表明,香芹醛可能是一种潜在的抗癌治疗药物。

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