首页> 外文期刊>Chemotherapy: International Journal of Experimental and Clinical Chemotherapy >Topoisomerase I inactivation by reticulol and its in vivo cytotoxicity against B16F10 melanoma.
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Topoisomerase I inactivation by reticulol and its in vivo cytotoxicity against B16F10 melanoma.

机译:网状酚使拓扑异构酶I失活及其对B16F10黑色素瘤的体内细胞毒性。

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摘要

To investigate the enzyme-inhibitory efficacy and the cytotoxicity of reticulol produced from a strain of Streptoverticillium, we conducted a DNA topoisomerase (Topo) cleavage assay and an in vivo assay using B16F10 melanoma. From the inhibition assay of reticulol for Topo I, which is involved in melanoma metastasis, it was seen that Topo I treated with 45 microM reticulol did not replicate or transcribe DNA by forming supercoiled DNA. In the annexin V/propidium iodide staining assay to investigate the death pattern of B16F10 cells treated with 200 microM reticulol, proliferation of B16F10 cells was inhibited due to necrosis. Furthermore, from the in vivo assay, reticulol combined with Adriamycin (a mixture with retinolol 5 mg/kg and Adriamycin 1 mg/kg) further retarded the tumor growth compared to that in mice treated with Adriamycin alone (1 mg/kg). The survival rate of tumor-bearing mice treated with the mixture was closely associated with its cytotoxicity. Taken together, these results suggested that reticulol inactivates Topo I, which is involved in tumor metastasis, and exhibits excellent cytotoxic efficacy against B16F10 melanoma, when combined with Adriamycin, in a mouse model.
机译:为了研究链霉菌属菌株生产的网状粗蛋白的酶抑制功效和细胞毒性,我们进行了DNA拓扑异构酶(Topo)裂解试验和使用B16F10黑色素瘤的体内试验。从网状蛋白对涉及黑色素瘤转移的Topo I的抑制试验中,可以看出用45 microM网状蛋白处理的Topo I不会通过形成超螺旋DNA而复制或转录DNA。在膜联蛋白V /碘化丙啶染色试验中,研究了用200 microM网红处理的B16F10细胞的死亡模式,由于坏死抑制了B16F10细胞的增殖。此外,从体内试验来看,与单独用阿霉素(1 mg / kg)治疗的小鼠相比,网状甜菊醇联合阿霉素(视黄醇5 mg / kg和阿霉素1 mg / kg的混合物)进一步延迟了肿瘤的生长。用该混合物处理的荷瘤小鼠的存活率与其细胞毒性密切相关。综上所述,这些结果表明,在小鼠模型中,当与阿霉素联合使用时,网状酚灭活参与肿瘤转移的Topo I,并且对B16F10黑色素瘤表现出优异的细胞毒性。

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