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咖啡酸苯乙酯能否增强他莫昔芬对乳腺癌的抗肿瘤作用?

Could Caffeic Acid Phenethyl Ester Expand the Antitumor Effect of Tamoxifen in Breast Carcinoma?

作者信息

Motawi Tarek K, Abdelazim Samy A, Darwish Hebatallah A, Elbaz Eman M, Shouman Samia A

机构信息

a Department of Biochemistry , Faculty of Pharmacy, Cairo University , Cairo , Egypt.

b Department of Cancer Biology , National Cancer Institute, Cairo University , Cairo , Egypt.

出版信息

Nutr Cancer. 2016;68(3):435-45. doi: 10.1080/01635581.2016.1153669. Epub 2016 Mar 23.

Abstract

Despite tamoxifen (TAM) is beneficial in treating a significant proportion of patients with breast cancer, many women still relapse after long-term therapy. Caffeic acid phenethyl ester (CAPE) is a component of honeybee propolis, with a plethora of important biological actions including anticancer activity. This study aimed to explore the cytotoxicity, the type of drugs interaction as well as the apoptotic and autophagic pathways of the combined treatment of TAM and CAPE in MCF-7 cells. Their antitumor activity and effect on survival of mice bearing Ehrlich tumor were also analyzed. The results showed synergistic cytotoxic effects, manifested by significant activation of apoptotic machinery, along with downregulation of protein levels of Bcl-2 and beclin-1, upon using the combination regimen. However, the ratio between microtubule-associated protein light chain 3-II and -I was not altered. Moreover, a decrease in vascular endothelial growth factor level was detected. Similarly, TAM + CAPE increased the life span of tumor-bearing animals and caused a marked regression in their tumor size and weight compared with those treated with either TAM or CAPE alone. In conclusion, CAPE relatively improved the anticancer activity of TAM in both in vitro and in vivo models via its apoptotic and angiostatic potentials.

摘要

尽管他莫昔芬(TAM)对很大一部分乳腺癌患者的治疗有益,但许多女性在长期治疗后仍会复发。咖啡酸苯乙酯(CAPE)是蜜蜂蜂胶的一种成分,具有大量重要的生物学作用,包括抗癌活性。本研究旨在探讨TAM和CAPE联合处理对MCF-7细胞的细胞毒性、药物相互作用类型以及凋亡和自噬途径。还分析了它们的抗肿瘤活性以及对荷艾氏瘤小鼠生存的影响。结果显示,联合用药方案具有协同细胞毒性作用,表现为凋亡机制的显著激活,同时Bcl-2和beclin-1蛋白水平下调。然而,微管相关蛋白轻链3-II与-I的比例未发生改变。此外,检测到血管内皮生长因子水平降低。同样,与单独使用TAM或CAPE治疗的动物相比,TAM + CAPE延长了荷瘤动物的寿命,并使其肿瘤大小和重量显著减小。总之,CAPE通过其凋亡和血管生成抑制潜能,在体外和体内模型中相对提高了TAM的抗癌活性。

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