Tumor cell drug resistance and its reversal.

A Mansouri, K J Henle, W A Nagle, A J Moss
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Abstract

Tumors that formerly were uniformly fatal can now be cured by cancer chemotherapy. However, successful anticancer therapy is faced by many obstacles, such as excessive normal tissue toxicity and drug resistance. Tumor drug resistance may be either intrinsic or acquired. The multidrug resistance (MDR) is a unique phenomenon and is characterized by tumor resistance to various structurally unrelated drugs. Known mechanisms for MDR include overexpression of a membrane P-glycoprotein 170 and elevated cellular levels of reducing agents, such as glutathione (GSH). Currently available strategies for overcoming drug resistance include competitive inhibitors of the P-glycoprotein 170, inhibitors of GSH synthesis, and adjuvant therapy with hyperthermia. Development of drug resistance is analogous to a physiological detoxification mechanism and may continue to limit the effectiveness of cancer chemotherapy in the near future.

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肿瘤细胞耐药及其逆转。
以前致命的肿瘤现在可以通过癌症化疗来治愈。然而,成功的抗癌治疗面临着许多障碍,如过度的正常组织毒性和耐药性。肿瘤耐药可能是内在的,也可能是获得性的。多药耐药(MDR)是一种独特的现象,其特征是肿瘤对多种结构无关的药物产生耐药性。已知的多药耐药机制包括膜p糖蛋白170的过度表达和细胞还原剂水平的升高,如谷胱甘肽(GSH)。目前克服耐药的有效策略包括p -糖蛋白170的竞争性抑制剂、GSH合成抑制剂和热疗辅助治疗。耐药性的发展类似于生理解毒机制,并可能在不久的将来继续限制癌症化疗的有效性。
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