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恶性黑色素瘤中P-糖蛋白的表达

p-glycoprotein expression in malignant melanoma.

作者信息

Fuchs B, Ostmeier H, Suter L

机构信息

Fachklinik Hornheide, Münster, Federal Republic of Germany.

出版信息

J Cancer Res Clin Oncol. 1991;117(2):168-71. doi: 10.1007/BF01613142.

Abstract

In some human malignancies resistance to chemotherapy is caused by an energy-dependent efflux system, responsible for the removal of chemotherapeutics out of the resistant tumor cells. A major component of this efflux system is the permeability glycoprotein (p-glycoprotein), which depends on the multidrug-resistance gene MDR1. We have tested p-glycoprotein in primary and metastatic human melanoma by use of the monoclonal antibody C219; a substantial expression was only observed in 1/37 primary melanomas and in 1/27 melanoma metastases. None of the patients with negative metastases responded to chemotherapy. Moreover a complete remission of metastatic growth was observed in the patient with the metastasis significantly expressing the p-glycoprotein. Sequential studies revealed no significant increase of p-glycoprotein-positive cells during and after chemotherapy. We conclude that drug resistance in human melanoma does not usually depend on the p-glycoprotein-related efflux system. Other mechanisms are obviously responsible for drug resistance in this human malignancy.

摘要

在一些人类恶性肿瘤中,对化疗的耐药性是由一种能量依赖性外排系统引起的,该系统负责将化疗药物排出耐药肿瘤细胞。这种外排系统的一个主要成分是通透性糖蛋白(p-糖蛋白),它依赖于多药耐药基因MDR1。我们使用单克隆抗体C219检测了原发性和转移性人类黑色素瘤中的p-糖蛋白;仅在1/37的原发性黑色素瘤和1/27的黑色素瘤转移灶中观察到大量表达。转移灶为阴性的患者均对化疗无反应。此外,在转移灶中p-糖蛋白显著表达的患者中观察到转移瘤生长完全缓解。序贯研究显示,化疗期间及化疗后p-糖蛋白阳性细胞无显著增加。我们得出结论,人类黑色素瘤的耐药性通常不依赖于与p-糖蛋白相关的外排系统。其他机制显然是导致这种人类恶性肿瘤耐药性的原因。

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