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Synergistic inhibition of malignant melanoma proliferation by melphalan combined with ultrasound and microbubbles

机译:美法仑联合超声和微泡协同抑制恶性黑色素瘤增殖

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摘要

The cavitational effects of ultrasound (US) exposure induce transient pores on the cell membrane (sonoporation). Sonoporation have been applied in the field of cancer therapy by promoting delivery of extracellular molecules such as drugs and genes into cytoplasm. In addition, it is known that using US together with microbubbles (MB) elevates permeability of these agents. In this study, by applying the US-MB strategy for melanoma chemotherapy, we evaluated the antitumor effect of melphalan combined with US-MB on a melanoma cell line (C32) in vitro and in vivo. The in vitro cytotoxic effect of the melphalan with US-MB was greater than that of melphalan alone or melphalan in combination with US. In vivo experiments using xenografts, intratumoral injection of melphalan and MB with US exposure led to a greater degree of tumor regression than did the intratumoral injection of the melphalan alone or melphalan in combination with US. These results suggest that US-MB promotes the antitumor effect of melphalan by increasing delivery of molecules into cells and that this strategy may become an effective method of adjuvant therapy against malignant melanoma.
机译:超声(US)暴露的空化作用会在细胞膜上引起瞬时气孔(sonoporation)。通过促进将诸如药物和基因之类的细胞外分子传递到细胞质中,Sonoporation已应用于癌症治疗领域。另外,已知将US与微泡(MB)一起使用可提高这些试剂的渗透性。在这项研究中,通过将US-MB策略应用于黑色素瘤化疗,我们评估了美法仑联合US-MB在体外和体内对黑色素瘤细胞系(C32)的抗肿瘤作用。美法仑与US-MB的体外细胞毒性作用大于单独美法仑或美法仑与US联合使用的情况。使用异种移植的体内实验,与单独的美法仑或美法仑联合US的瘤内注射相比,美法的瘤内注射美法仑和MB导致的肿瘤消退程度更高。这些结果表明,US-MB通过增加分子向细胞中的递送来促进美法仑的抗肿瘤作用,并且该策略可能成为针对恶性黑素瘤的辅助治疗的有效方法。

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