Recent progress in P-glycoprotein research.

Anti-cancer drug design Pub Date : 1999-04-01
K Ueda, A Yoshida, T Amachi
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引用次数: 0

Abstract

P-glycoprotein can extrude a variety of structurally diverse, toxic xenobiotic compounds from cells. It is believed to be one of key molecules which can cause multidrug resistance in cancer. This paper deals with recent progress in P-glycoprotein research, especially in its structure, mechanisms for substrate recognition and transport. The review also discusses specific modulators of multidrug resistance in cancer and gene therapy using the MDR1 gene.

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p -糖蛋白研究进展。
p -糖蛋白可以从细胞中挤出多种结构多样、有毒的异种化合物。它被认为是引起癌症多药耐药的关键分子之一。本文综述了近年来p -糖蛋白的结构、底物识别和转运机制等方面的研究进展。本文还讨论了肿瘤多药耐药的特异性调节因子和利用MDR1基因进行基因治疗。
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Linker length in podophyllotoxin-acridine conjugates determines potency in vivo and in vitro as well as specificity against MDR cell lines. Topoisomerase I/II selectivity among derivatives of N-[2-(dimethylamino)ethyl]acridine-4-carboxamide (DACA). Synthesis and anticancer activity of nordihydroguaiaretic acid (NDGA) and analogues. Cyclohexylamino-demethoxy-hypocrellin B and photodynamic therapy decreases human cancer in vitro. Photokilling of cultured tumour cells by the porphyrin derivative CF3.
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