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首页> 外文期刊>American journal of clinical dermatology >Tumor immunotherapy in melanoma: strategies for overcoming mechanisms of resistance and escape.
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Tumor immunotherapy in melanoma: strategies for overcoming mechanisms of resistance and escape.

机译:黑色素瘤的肿瘤免疫疗法:克服耐药性和逃逸机制的策略。

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The incidence of melanoma has been steadily increasing over the last 3 decades. Currently, there are several approved treatments for metastatic melanoma, including chemotherapy and biologic therapy as both single treatments and in combination, but none is associated with a significant increase in survival. The chemotherapeutic agent dacarbazine is the standard treatment for metastatic melanoma, with a response rate of 15-20%, although most responses are not sustained. One of the main problems with melanoma treatment is chemotherapeutic resistance. The mechanisms of resistance of melanoma cells to chemotherapy have yet to be elucidated. Following treatment with dacarbazine, melanoma cells activate the extracellular signal-regulated kinase pathway, which results in over-expression and secretion of interleukin (IL)-8 and vascular endothelial growth factor. Melanoma cells utilize this mechanism to escape from the cytotoxic effect of the drug. We have previously reported on the development of fully human neutralizing antibodies against IL-8 (anti-IL-8-monoclonal-antibody [ABX-IL8]). In preclinical studies, ABX-IL8 inhibited tumor growth, angiogenesis, and metastasis of human melanoma in vivo. We propose that combination treatment with dacarbazine and IL-8 will potentiate the cytotoxic effect of the drug. Furthermore, formation of metastasis is a multistep process that includes melanoma cell adhesion to endothelial cells. Melanoma cell adhesion molecule (MUC18) mediates these processes in melanoma and is therefore a good target for eliminating metastasis. We have developed a fully human antibody against MUC18 that has shown promising results in preclinical studies. Since resistance is one of the major obstacles in the treatment of melanoma, we propose that utilization of antibodies against IL-8 or MUC18 alone, or as part of a 'cocktail' in combination with dacarbazine, may be a new treatment modality for metastatic melanoma that overcomes resistance of the disease to chemotherapy and significantly improves survival of patients.
机译:在过去的三十年中,黑色素瘤的发病率一直在稳定增长。目前,已经有几种批准的转移性黑色素瘤治疗方法,包括化学疗法和生物疗法,既可作为单一疗法,也可作为联合疗法,但均未与生存率显着提高相关。化疗药物达卡巴嗪是转移性黑色素瘤的标准治疗方法,尽管大多数反应不能持续,但反应率为15-20%。黑色素瘤治疗的主要问题之一是化疗耐药性。黑色素瘤细胞对化学疗法的耐药机制尚未阐明。用达卡巴嗪治疗后,黑素瘤细胞激活细胞外信号调节的激酶途径,导致白介素(IL)-8和血管内皮生长因子的过度表达和分泌。黑色素瘤细胞利用这种机制来逃避药物的细胞毒性作用。我们先前曾报道过针对IL-8的完全人中和抗体(抗IL-8单克隆抗体[ABX-IL8])的开发。在临床前研究中,ABX-IL8在体内抑制人黑素瘤的肿瘤生长,血管生成和转移。我们建议用达卡巴嗪和IL-8联合治疗将增强药物的细胞毒性作用。此外,转移的形成是一个多步骤过程,包括黑素瘤细胞粘附于内皮细胞。黑色素瘤细胞粘附分子(MUC18)在黑色素瘤中介导这些过程,因此是消除转移的良好靶标。我们已经开发了一种针对MUC18的完全人类抗体,在临床前研究中显示出令人鼓舞的结果。由于耐药性是治疗黑色素瘤的主要障碍之一,因此我们建议单独使用抗IL-8或MUC18的抗体,或与达卡巴嗪组合使用作为“鸡尾酒”的一部分,可能是转移性黑色素瘤的一种新治疗方法。克服了疾病对化学疗法的抵抗力并显着提高了患者的生存率。

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