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Modification of topoisomerases in mammospheres derived from breast cancer cell line: clinical implications for combined treatments with tyrosine kinase inhibitors

机译:源自乳腺癌细胞系的乳腺球体内拓扑异构酶的修饰:酪氨酸激酶抑制剂联合治疗的临床意义

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摘要

BackgroundAccumulating evidences suggest that tumors are driven by a small population of cells, termed “cancer stem cells” (CSCs), which may be resistant to current therapeutic approaches. In breast carcinoma, the CSCs have been identified as a CD44+/CD24 cell population. These rare cells are able to grow as non-adherent sphere-like structures, termed “mammospheres”, which enables their isolation and expansion in culture. To design efficient strategies for the complete eradication of CSCs, it is important to identify enzymes and proteins that are known as anti-cancer targets, and differ in their properties from those present in the none CSCs. Here we investigated the activity and expression of type I and type II DNA topoisomerases (topo I and topo II) in CSCs and their response to anti-topoisomerase inhibitors.
机译:背景技术越来越多的证据表明,肿瘤是由一小部分细胞(称为“癌症干细胞”(CSC))驱动的,这些细胞可能对当前的治疗方法产生抵抗力。在乳腺癌中,CSC已被鉴定为CD44 + / CD24 -细胞群。这些稀有细胞能够以非粘附球状结构(称为“哺乳动物球”)生长,从而使其能够在培养物中分离和扩增。要设计用于彻底根除CSC的有效策略,重要的是要鉴定被称为抗癌靶标的酶和蛋白,这些酶和蛋白的特性与无CSC的酶和蛋白不同。在这里,我们研究了CSC中I型和II型DNA拓扑异构酶(拓扑I和拓扑II)的活性和表达以及它们对抗拓扑异构酶抑制剂的反应。

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