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Anti-tumour pharmaceutical compositions capable of reducing drug resistance in tumour cells
Anti-tumour pharmaceutical compositions capable of reducing drug resistance in tumour cells
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机译:能够降低肿瘤细胞耐药性的抗肿瘤药物组合物
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摘要
The invention refers to compositions containing chemotherapy agents frequently used in cancer therapy, such as etoposide and cisplatin, in combination with an inhibitor of the interleukin 6 receptor complex signalling by gp130. Such compositions decrease the drug resistance of a tumour cell line. A specific embodiment of the invention uses a superantagonist of interleukin 6, the mutein of IL-6, Sant 7 and reported in the sequence listing as SEQ ID NO:1, which is capable of binding the sub-unit IL6-R alpha of the IL-6 receptor. Sant 7 indicated inhibits binding, by steric blocking, with the sub-unit gp130 of the IL-6 receptor complex. Transduction of the signal from this cytokine is in fact involved in the multiple drug resistance mechanisms that are typically developed by tumour cells following chemotherapy.
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机译:本发明涉及包含通常用于癌症治疗的化疗剂例如依托泊苷和顺铂的组合物,其与通过gp130的白介素6受体复合物信号转导的抑制剂组合。这样的组合物降低了肿瘤细胞系的耐药性。本发明的一个具体实施方案使用白介素6的超拮抗剂,IL-6,Sant 7的突变蛋白,并在序列表中以SEQ ID NO:1报道,其能够结合其的亚基IL6-Rα。 IL-6受体。指出的Sant 7通过空间阻断抑制了与IL-6受体复合物的亚基gp130的结合。实际上,来自这种细胞因子的信号转导涉及多种耐药机制,这些机制通常是肿瘤细胞在化疗后产生的。
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