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抗肿瘤葱属硫化物。

Antitumor Allium Sulfides.

作者信息

Nohara Toshihiro, Fujiwara Yukio, El-Aasr Mona, Ikeda Tsuyoshi, Ono Masateru, Nakano Daisuke, Kinjo Junei

机构信息

Faculty of Pharmaceutical Sciences, Sojo University.

出版信息

Chem Pharm Bull (Tokyo). 2017;65(3):209-217. doi: 10.1248/cpb.c16-00844.

Abstract

We examined the sulfides in onion (Allium cepa L.), Welsh onion (A. fistulosum L.), and garlic (A. sativum L.), and obtained three new thiolane-type sulfides (onionins A-A) from onion; two new thiabicyclic-type sulfides (welsonins A, A), together with onionins A-A, from Welsh onion; and six new acyclic-type sulfides (garlicnins L-1-L-4, E, and F), ten new thiolane-type sulfides (garlicnins A, B-B, C-C, K, and K), and three new atypical cyclic-type sulfides (garlicnins G, I, and J) from garlic. Acetone extracts showed the potential of these sulfides in inhibiting the polarization of M2 activated macrophages that are capable of suppressing tumor-cell proliferation. The effect of the thiolane-type sulfide of a major component, onionin A, on tumor progression and metastasis in both osteosarcoma and ovarian cancer-bearing mouse models was then examined. Tumor proliferation was depressed, and tumor metastasis was controlled by regulating macrophage activation. These results showed that onionin A is an effective agent for controlling tumors in both in vitro and in vivo models, and that the antitumor effects observed in vivo are likely caused by reversing the antitumor immune system. Activation of the antitumor immune system by onionin A might be an effective adjuvant therapy for patients with osteosarcoma, ovarian cancer and other malignant tumors. Based on these findings, pharmacological investigations will be conducted in the future to develop natural and healthy foods and anti-cancer agents that can prevent or combat disease.

摘要

我们研究了洋葱(Allium cepa L.)、大葱(A. fistulosum L.)和大蒜(A. sativum L.)中的硫化物,从洋葱中获得了三种新的硫杂环戊烷型硫化物(洋葱素A - A);从大葱中获得了两种新的硫杂双环型硫化物(大葱素A、A)以及洋葱素A - A;从大蒜中获得了六种新的无环型硫化物(大蒜素L - 1 - L - 4、E和F)、十种新的硫杂环戊烷型硫化物(大蒜素A、B - B、C - C、K和K)以及三种新的非典型环型硫化物(大蒜素G、I和J)。丙酮提取物显示这些硫化物具有抑制能够抑制肿瘤细胞增殖的M2活化巨噬细胞极化的潜力。然后研究了主要成分洋葱素A的硫杂环戊烷型硫化物对骨肉瘤和荷卵巢癌小鼠模型中肿瘤进展和转移的影响。肿瘤增殖受到抑制,肿瘤转移通过调节巨噬细胞活化得到控制。这些结果表明,洋葱素A在体外和体内模型中都是控制肿瘤的有效药物,并且在体内观察到的抗肿瘤作用可能是由逆转抗肿瘤免疫系统引起的。洋葱素A激活抗肿瘤免疫系统可能是骨肉瘤、卵巢癌和其他恶性肿瘤患者的一种有效辅助治疗方法。基于这些发现,未来将进行药理学研究,以开发能够预防或对抗疾病的天然健康食品和抗癌药物。

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