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新型蒽环类药物ID-6105在SK-OV-3卵巢癌细胞中大量细胞内蓄积。

Extensive intracellular accumulation of ID-6105, a novel anthracycline, in SK-OV-3 ovarian cancer cells.

作者信息

Shin Dae Hwan, Choi Kyu Seok, Park Sang-Ae, Cho Byung Suk, Lee Hong-Sub, Ryu Jung-Su, Kim Tae-Yong, Lee Chong-Kil, Song Sukgil, Chung Youn Bok

机构信息

National Research Laboratory of PK/PD, CBITRC, Biotechnology Research Institute, College of Pharmacy, Chungbuk National University, Cheongju, Chungbuk 361-763, Korea.

出版信息

Arch Pharm Res. 2008 Oct;31(10):1355-61. doi: 10.1007/s12272-001-2117-y. Epub 2008 Oct 29.

Abstract

We investigated the anticancer activity of 11-hydroxyaclacinomycin X (ID-6105), a novel anthracycline, on weakly doxorubicin (Dox)-resistant SK-OV-3 ovarian cancer cells, and elucidated the relationship between its anticancer activity and accumulation in cells compared with those of Dox. Accumulation of ID-6105 in the cells was time-and concentration-dependent, a result of drug-induced cytotoxicity in the cells. SK-OV-3 cells were preloaded with ID-6105 or Dox for 12 h at concentrations ranging from 100 to 2000 nM and then incubated with drug-free medium for 0-48 h. Cell viability was measured using a proliferation-based assay (XTT assay). The inhibitory effects of ID-6105 on cell viability were more pronounced than those of Dox. The IC(50) values of ID-6105 after 24-and 48-h incubation with drug-free medium were 1.58 and 0.084 microM, while those of Dox were 2 and 0.334 microM, respectively. To investigate the relationship between the intracellular levels and the cytotoxic effects of the drugs, we preloaded SKOV-3 cells with ID-6105 or Dox (100-2000 nM) for 12 h and then measured the intracellular levels of drugs by HPLC in drug-free medium for 0-48 h. After preloading the drugs, the intracellular concentrations of ID-6105 at time 0 were 1.3-, 1.8-, and 1.4-fold larger than those of Dox at initial concentrations of 500, 1000, and 2000 nM, respectively. The extent of ID-6105 accumulation in the cells was more pronounced than that of Dox. These findings suggest that ID-6105 effluxed less from the cells than Dox, resulting in its extensive cytotoxicity compared with that of Dox. These results show that accumulation of ID-6105 within tumor cells may be important for the inhibitory effects of this drug in cancer cells. ID-6105 has an antiproliferative effect on SK-OV-3 cells that is due to its cytotoxicity. This effect is more pronounced than that of Dox, and may be attributed to extensive accumulation of ID-6105 in the cells.

摘要

我们研究了新型蒽环类药物11-羟基阿克拉霉素X(ID-6105)对阿霉素(Dox)低度耐药的SK-OV-3卵巢癌细胞的抗癌活性,并阐明了其抗癌活性与细胞内蓄积之间的关系,并与阿霉素进行了比较。ID-6105在细胞内的蓄积呈时间和浓度依赖性,这是药物诱导细胞毒性的结果。将SK-OV-3细胞在100至2000 nM的浓度下用ID-6105或阿霉素预加载12小时,然后在无药物培养基中孵育0至48小时。使用基于增殖的检测方法(XTT检测)测量细胞活力。ID-6105对细胞活力的抑制作用比阿霉素更明显。在无药物培养基中孵育24小时和48小时后,ID-6105的IC50值分别为1.58和0.084 microM,而阿霉素的IC50值分别为2和0.334 microM。为了研究细胞内药物水平与细胞毒性作用之间的关系,我们将SKOV-3细胞用ID-6105或阿霉素(100-2000 nM)预加载12小时,然后在无药物培养基中0至48小时内通过HPLC测量细胞内药物水平。预加载药物后,在初始浓度为500、1000和2000 nM时,ID-6105在时间0时的细胞内浓度分别比阿霉素高1.3倍、1.8倍和1.4倍。ID-6105在细胞内的蓄积程度比阿霉素更明显。这些发现表明,与阿霉素相比,ID-6105从细胞中流出的较少,从而导致其具有广泛的细胞毒性。这些结果表明,ID-6105在肿瘤细胞内的蓄积可能对该药物在癌细胞中的抑制作用很重要。ID-6105对SK-OV-3细胞具有抗增殖作用,这是由于其细胞毒性。这种作用比阿霉素更明显,可能归因于ID-6105在细胞内的广泛蓄积。

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