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Liposome encapsulation of doxorubicin and celecoxib in combination inhibits progression of human skin cancer cells

机译:阿霉素和塞来昔布联合脂质体包裹抑制人皮肤癌细胞的发展

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摘要

Therapeutic agents aimed at inhibiting a single molecular target have not been successful in cancer therapy, but rather they impart resistance. However, multi-target inhibitors have shown promising results in circumventing the development of resistance and inducing apoptosis in cancer cells/tissues. In this study, we encapsulated doxorubicin and celecoxib in a single liposome at a ratio of 1:10. These dual drug-encapsulated liposomes showed excellent anticancer activity compared to individually encapsulated liposomes. The expression of key proteins such as AKT and COX-2 was suppressed, which suggests that doxorubicin and celecoxib synergistically inhibit multiple key signaling pathways.
机译:旨在抑制单个分子靶标的治疗剂在癌症治疗中并未取得成功,而是赋予了抵抗力。然而,多靶点抑制剂在规避耐药性的发展并诱导癌细胞/组织中的凋亡方面显示出令人鼓舞的结果。在这项研究中,我们将阿霉素和塞来昔布以1:10的比例封装在单个脂质体内。与单独包封的脂质体相比,这些双重药物包封的脂质体显示出优异的抗癌活性。关键蛋白如AKT和COX-2的表达被抑制,这表明阿霉素和塞来昔布协同抑制多种关键信号通路。

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