首页> 外文期刊>Toxicology in vitro: an international journal published in association with BIBRA >Anticancer properties of 10-hydroxycamptothecin in a murine melanoma pulmonary metastasis model in vitro and in vivo.
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Anticancer properties of 10-hydroxycamptothecin in a murine melanoma pulmonary metastasis model in vitro and in vivo.

机译:10-羟基喜树碱在小鼠黑素瘤肺转移模型中的体内外抗癌特性。

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摘要

Lung cancer, including lung metastatic cancer, remains one of the most difficult types of cancer to treat. Therefore, the search for new agents for its treatment is very important. 10-Hydroxycamptothecin (HCPT) was proved to have ideal anticancer activity in curing series cancer cells. In this study, the anticancer effect of HCPT on melanoma lung metastasis cancer was investigated by several administration routes, and whether the effect may be attributed to the induction of tumor cells apoptosis was determined. MTT assay results showed that HCPT exhibited selective cytotoxic activity against B16-F10 cells in a concentration- and time-dependent manner. Hoechst 33258 staining and transmission electron microscopy showed typical apoptotic morphology such as condensed chromatin, irregular nuclei, and apoptotic body formation. Flow cytometry analysis indicated a growth on apoptotic cells and a cell-cycle arrest in S phase after treatment with HCPT. In vivo melanoma pulmonary metastases were inhibited by treatment with HCPT. A more significant inhibition was observed if HCPT was administered by aerosol inhalation than that given by i.v. or i.p. administration. Thus, HCPT exhibited potential anticancer activity against B16-F10 cells in vitro and in vivo. However, the possible mechanisms involved still need to be investigated to explain this behavior.
机译:肺癌,包括肺转移癌,仍然是最难治疗的癌症之一。因此,寻找新的治疗药物非常重要。已证明10-羟基喜树碱(HCPT)在治疗系列癌细胞中具有理想的抗癌活性。在这项研究中,通过多种给药途径研究了HCPT对黑色素瘤肺转移癌的抗癌作用,并确定了该作用是否可归因于诱导肿瘤细胞凋亡。 MTT测定结果表明,HCPT对B16-F10细胞表现出选择性的细胞毒活性,呈浓度和时间依赖性。 Hoechst 33258染色和透射电镜显示典型的凋亡形态,例如染色质浓缩,核不规则和凋亡小体形成。流式细胞仪分析表明,用HCPT处理后,凋亡细胞的生长和S期的细胞周期停滞。体内黑色素瘤的肺转移受到HCPT治疗的抑制。如果通过气雾吸入施用HCPT,则比i.v.给予的抑制作用更显着。或i.p.行政。因此,HCPT在体外和体内均显示出对B16-F10细胞的潜在抗癌活性。但是,仍需要调查可能的机制来解释此行为。

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