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丹参根中环三萜 C 对细胞增殖的抑制作用及诱导细胞凋亡

Antiproliferative activity and apoptosis induction by trijuganone C isolated from the root of Salvia miltiorrhiza Bunge (Danshen).

机构信息

Department of Pharmacognosy, Faculty of Pharmaceutical Sciences, Nagasaki International University, Nagasaki, 859-3298, Japan.

School of Medicine and Pharmacy, Vietnam National University, Hanoi, Hanoi, Vietnam.

出版信息

Phytother Res. 2018 Apr;32(4):657-666. doi: 10.1002/ptr.6013. Epub 2018 Feb 21.

DOI:10.1002/ptr.6013
PMID:29464799
Abstract

In this study, we found that the hexane fraction of Danshen, the dried root of Salvia miltiorrhiza (Lamiaceae), exerted antiproliferative effects on human leukemia cells. Phytochemical investigation of the hexane fraction achieved the isolation of the tanshinone diterpenes: dihydrotanshinone I (1), trijuganone C (2), trijuganone B (3), cryptotanshinone (4), tanshinone IIA (5), and tanshinone I (6). Compound 2 showed significant antiproliferative activities against human leukemia cells HL-60, Jurkat, and U937. The antiproliferative activities of 2 against human cancer and normal cells indicated that 2 exhibited potent antiproliferative activities with IC values less than 10 μM against HL-60 and Jurkat cells as well as on the colon cancer cells DLD-1, COLO 205, and Caco-2. Compound 2 induced chromatin condensation, DNA fragmentation, activation of caspase-3, -8, and -9, and the cleavage of poly (ADP-ribose) polymerase (PARP) in HL-60 cells. Moreover, 2 activated Bid and Bax, leading to the loss of mitochondrial membrane potential, and 2 induced the cytochrome c release from mitochondria into cytosol. In contrast, Bcl-2 and Bcl-xL were unaffected by 2. These results suggest that 2 exerts antiproliferative effects via apoptosis induction mediated by mitochondrial dysfunction and caspase activation. Compound 2 may serve as a candidate of potential chemotherapeutic agent for human leukemia.

摘要

在这项研究中,我们发现丹参的正己烷部位,即唇形科丹参的干燥根,对人白血病细胞具有抗增殖作用。正己烷部位的植物化学研究实现了丹参酮二萜的分离:二氢丹参酮 I(1)、三丹参酮 C(2)、三丹参酮 B(3)、隐丹参酮(4)、丹参酮 IIA(5)和丹参酮 I(6)。化合物 2 对人白血病细胞 HL-60、Jurkat 和 U937 表现出显著的抗增殖活性。2 对人癌细胞和正常细胞的抗增殖活性表明,2 对 HL-60 和 Jurkat 细胞具有很强的抗增殖活性,IC 值小于 10μM,对结肠癌细胞 DLD-1、COLO 205 和 Caco-2 也有活性。化合物 2 诱导 HL-60 细胞染色质浓缩、DNA 片段化、caspase-3、-8 和 -9 的激活以及多聚(ADP-核糖)聚合酶(PARP)的切割。此外,2 激活 Bid 和 Bax,导致线粒体膜电位丧失,2 诱导细胞色素 c 从线粒体释放到细胞质中。相反,Bcl-2 和 Bcl-xL 不受 2 的影响。这些结果表明,2 通过线粒体功能障碍和半胱天冬酶激活介导的细胞凋亡诱导发挥抗增殖作用。化合物 2 可能成为治疗人类白血病的潜在化疗药物的候选物。

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