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桦木醇作为一种抗肿瘤剂,在体外对A431、HeLa和MCF7细胞系进行了测试,并在鸡胚绒毛尿囊膜实验中作为体内血管生成抑制剂进行了测试。

Betulin as an antitumor agent tested in vitro on A431, HeLa and MCF7, and as an angiogenic inhibitor in vivo in the CAM assay.

作者信息

Dehelean Cristina Adriana, Feflea Stefana, Molnár Judit, Zupko Istvan, Soica Codruta

机构信息

Faculty ofPharmacy, Victor Babes University of Medicine and Pharmacy, Timişoara, Romania 300041.

出版信息

Nat Prod Commun. 2012 Aug;7(8):981-5.

Abstract

Betulin, an important compound found in birch tree bark, can be converted to betulinic acid, an important pharmacological substance. Betulin has recently been reported as a cytotoxic agent for several tumor cell lines and as an apoptotic inductor. Angiogenesis is a key process involved in tumor metastasis and in developing tumor resistance to cytotoxic therapy. There are little data on betulin as an anti angiogenic agent. This preliminary study aimed to evaluate the cytotoxic effect of betulin on three cancer cell lines: HeLa (cervix adenocarcinoma), MCF7 (breast adenocarcinoma) and A431 (skin epidermoid carcinoma), and the apoptotic mechanism, as well as the implication in the capillary formation of the chicken embryo chorioallantoic membrane. The analysis consisted in the interpretation of the MTT assay and fluorescence double staining with Hoechst dye 33258 and propidium iodide, while the angiogenic effect was evaluated using morphological and immunohistochemical techniques. The antitumor activity is revealed by the double fluorescence staining, indicating that at higher concentrations, the cell membrane permeability is enhanced, while at lower concentrations there is evidence for nuclear fragmentation. In what concerns its effect on the process of blood vessel formation, betulin induced the reduction of newly formed capillaries, especially in the mesenchyme, possible through targeting the normal function of endothelial cells. In vitro results proved the superior specificity of betulin on cervical cancer cells, followed by skin cancer cells.

摘要

桦木醇是白桦树皮中发现的一种重要化合物,可转化为桦木酸,一种重要的药理物质。最近有报道称桦木醇是几种肿瘤细胞系的细胞毒性剂和凋亡诱导剂。血管生成是肿瘤转移和肿瘤对细胞毒性治疗产生抗性过程中的一个关键过程。关于桦木醇作为抗血管生成剂的数据很少。这项初步研究旨在评估桦木醇对三种癌细胞系的细胞毒性作用:HeLa(宫颈腺癌)、MCF7(乳腺腺癌)和A431(皮肤表皮样癌),以及凋亡机制,以及对鸡胚绒毛尿囊膜毛细血管形成的影响。分析包括MTT试验的解读以及用Hoechst染料33258和碘化丙啶进行荧光双重染色,同时使用形态学和免疫组织化学技术评估血管生成作用。双重荧光染色显示了抗肿瘤活性,表明在较高浓度下,细胞膜通透性增强,而在较低浓度下,有核碎裂的证据。关于其对血管形成过程的影响,桦木醇诱导新形成的毛细血管减少,尤其是在间充质中,可能是通过靶向内皮细胞的正常功能实现的。体外结果证明了桦木醇对宫颈癌细胞具有更高的特异性,其次是皮肤癌细胞。

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