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基因扩增和酶的改变作为耐药性产生的机制。

Gene amplification and altered enzymes as mechanisms for the development of drug resistance.

作者信息

Bertino J R, Carman M D, Weiner H L, Cashmore A, Moroson B A, Srimatkandada S, Schornagel J H, Medina W D, Dube S K

出版信息

Cancer Treat Rep. 1983 Oct;67(10):901-4.

PMID:6354438
Abstract

Two known mechanisms by which neoplastic cells may become resistant to chemotherapeutic agents are reviewed, using methotrexate (MTX) resistance as a model. These mechanisms are an increased level of target enzyme, found in several instances to be a consequence of gene amplification, or an altered target enzyme or receptor, less capable of binding the drug. An example of MTX resistance due to low-level gene amplification in leukemia cells from an MTX-resistant patient is described. Strategies for selectively eradicating these resistant cell populations may be formulated based on the mechanism by which these cells became drug-resistant.

摘要

本文以甲氨蝶呤(MTX)耐药为模型,综述了肿瘤细胞对化疗药物产生耐药性的两种已知机制。这些机制包括:靶酶水平升高,在多种情况下是基因扩增的结果;或者靶酶或受体发生改变,使其与药物结合的能力降低。本文还描述了一名MTX耐药患者白血病细胞中因低水平基因扩增导致MTX耐药的实例。可根据这些细胞产生耐药性的机制,制定选择性根除这些耐药细胞群体的策略。

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