耐化疗肿瘤细胞的侵袭和转移。

Anna Nowakowska, Jolanta Tarasiuk
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引用次数: 5

摘要

转移性肿瘤耐药是恶性肿瘤临床治疗失败的主要原因。经常观察到,对原发肿瘤有活性的药物对具有改变信号通路的转移性肿瘤细胞不表现出相同的功效。参与多药耐药肿瘤细胞转移潜能发展的细胞因子包括一些癌蛋白、抗凋亡蛋白、突变抑制蛋白、整合素和CD44受体。研究还表明,许多化疗药物对肿瘤细胞的转移潜力和多药耐药(MDR)现象的出现有影响。大量研究结果表明,参与MDR发展和肿瘤细胞转移表型的基因受相同的信号通路调节。它们导致转录因子如HIF-1α、NF-κB、Ets1和AP-1的激活,这些转录因子控制着参与多药耐药肿瘤细胞转移潜能发展的基因的表达。确定导致耐多药肿瘤细胞转移潜力出现的关键细胞因素可能导致开发新的有效策略来治疗对传统化疗产生耐药性的转移性肿瘤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Invasion and metastasis of tumour cells resistant to chemotherapy.

Metastatic tumours resistant to chemotherapy are the major cause of the clinical failure in the treatment of malignant diseases. It is observed often that drugs active against primary tumours do not exhibit the same efficacy towards metastatic tumour cells having modified signaling pathways. Among cellular factors involved in the development of the metastatic potential of multidrug resistant tumour cells are some oncoproteins, antiapoptotic proteins, mutated suppressor proteins, integrins and CD44 receptor. It was also demonstrated that numerous chemotherapeutics have the effect on the emergence of the metastatic potential and multidrug resistance (MDR) phenomenon of tumour cells. The results of numerous studies suggest that genes involved in the development of MDR and metastatic phenotype of tumour cells are regulated by the same signaling pathways. They lead to the activation of transcription factors e.g. HIF-1α, NF-κB, Ets1 and AP-1 controlling the expression of genes involved in the development of the metastatic potential of multidrug resistant tumour cells. The identification of key cellular factors responsible for the emergence of the metastatic potential of MDR tumour cells could lead to the development of new efficient strategies for the treatment of metastatic tumours resistant to the conventional chemotherapy.

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