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蜜蜂蜂胶的抗癌活性:对咖啡酸苯乙酯及其与γ-环糊精复合物作用的功能见解

Anticancer Activity in Honeybee Propolis: Functional Insights to the Role of Caffeic Acid Phenethyl Ester and Its Complex With γ-Cyclodextrin.

作者信息

Ishida Yoshiyuki, Gao Ran, Shah Navjot, Bhargava Priyanshu, Furune Takahiro, Kaul Sunil C, Terao Keiji, Wadhwa Renu

机构信息

1 CycloChem Co, Ltd, Chuo-ku, Kobe, Japan.

2 National Institute of Advanced Industrial Science & Technology, Tsukuba, Japan.

出版信息

Integr Cancer Ther. 2018 Sep;17(3):867-873. doi: 10.1177/1534735417753545. Epub 2018 Feb 2.

Abstract

Besides honey, honeybees make a sticky substance (called propolis/bee glue) by mixing saliva with poplar tree resin and other botanical sources. It is known to be rich in bioactivities of which the anticancer activity is most studied. Caffeic acid phenethyl ester (CAPE) is a key anticancer component in New Zealand propolis. We have earlier investigated the molecular mechanism of anticancer activity in CAPE and reported that it activates DNA damage signaling in cancer cells. CAPE-induced growth arrest of cells was mediated by downregulation of mortalin and activation of p53 tumor suppressor protein. When antitumor and antimetastasis activities of CAPE were examined in vitro and in vivo, we failed to find significant activities, which was contrary to our expectations. On careful examination, it was revealed that CAPE is unstable and rather gets easily degraded into caffeic acid by secreted esterases. Interestingly, when CAPE was complexed with γ-cyclodextrin (γCD) the activities were significantly enhanced. In the present study, we report that the CAPE-γCD complex with higher cytotoxicity to a wide range of cancer cells is stable in acidic milieu and therefore recommended as an anticancer amalgam. We also report a method for preparation of stable and less-pungent powder of propolis that could be conveniently used for health and therapeutic benefits.

摘要

除了蜂蜜,蜜蜂还通过将唾液与杨树树脂及其他植物来源混合制成一种粘性物质(称为蜂胶/蜂蜡)。已知其富含生物活性成分,其中对其抗癌活性的研究最为深入。咖啡酸苯乙酯(CAPE)是新西兰蜂胶中的关键抗癌成分。我们之前研究了CAPE抗癌活性的分子机制,并报道它能激活癌细胞中的DNA损伤信号。CAPE诱导的细胞生长停滞是通过下调mortalin和激活p53肿瘤抑制蛋白介导的。当在体外和体内检测CAPE的抗肿瘤和抗转移活性时,我们未能发现显著活性,这与我们的预期相反。仔细检查后发现,CAPE不稳定,相当容易被分泌的酯酶降解为咖啡酸。有趣的是,当CAPE与γ-环糊精(γCD)复合时,其活性显著增强。在本研究中,我们报告了对多种癌细胞具有更高细胞毒性的CAPE-γCD复合物在酸性环境中稳定,因此推荐作为一种抗癌混合物。我们还报告了一种制备稳定且气味较淡的蜂胶粉末的方法,该方法可方便地用于健康和治疗益处。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1025/6142091/398442fd6d95/10.1177_1534735417753545-fig1.jpg

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