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广泛耐药表型。

The extended-MDR phenotype.

机构信息

Clinical Oncology Department, Royal North Shore Hospital, Bill Walsh Cancer Research Laboratories, St. Leonards, 2065, Australia.,

出版信息

Cytotechnology. 1998 Sep;27(1-3):237-47. doi: 10.1023/A:1008081208312.

Abstract

Cellular models have made a significant contribution to our understanding of the molecular mechanisms of resistance to chemotherapeutic drugs. However the vast majority of these models involve cell sublines with high levels of resistance generated by continuous exposure to high drug doses, and although the majority express a multidrug resistance (MDR) phenotype, they fall short of the broader drug cross resistance that is characteristic of cancers which no longer respond to treatment. Several studies have reported cell sublines which not only have the MDR phenotype and are resistant to 'natural product' lipophilic drugs, but they are also resistant to alkylating agents and antimetabolites. A common feature of these sublines is they were generated by treatment with low, clinically relevant levels of drug given intermittently. The term extended-MDR has been used to describe this type of broad drug cross resistance. Here we review those factors that promote the development of extended-MDR, the characteristics of extended-MDR sublines and the possible resistance mechanisms involved.

摘要

细胞模型为我们理解化疗药物耐药的分子机制做出了重大贡献。然而,这些模型绝大多数涉及通过持续暴露于高药物剂量产生高水平耐药性的细胞亚系,并且尽管大多数表达多药耐药 (MDR) 表型,但它们不能涵盖癌症对治疗不再敏感的更广泛的药物交叉耐药性。有几项研究报道了细胞亚系,它们不仅具有 MDR 表型并且对“天然产物”亲脂性药物具有耐药性,而且对烷化剂和抗代谢物也具有耐药性。这些亚系的一个共同特征是它们是通过以低剂量、临床相关水平间歇性给予药物治疗产生的。已经使用“扩展-MDR”这个术语来描述这种广泛的药物交叉耐药性。在这里,我们综述了促进扩展-MDR 发展的因素、扩展-MDR 亚系的特征以及可能涉及的耐药机制。

相似文献

1
The extended-MDR phenotype.广泛耐药表型。
Cytotechnology. 1998 Sep;27(1-3):237-47. doi: 10.1023/A:1008081208312.
3
Molecular mechanisms of multidrug resistance in cancer chemotherapy.癌症化疗中多药耐药的分子机制。
Pathol Res Pract. 1996 Jul;192(7):768-80. doi: 10.1016/S0344-0338(96)80099-9.

本文引用的文献

9
Extended multidrug resistance in haemopoietic cells.造血细胞中的广泛多药耐药性。
Br J Haematol. 1996 Dec;95(4):587-95. doi: 10.1046/j.1365-2141.1996.d01-1951.x.

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