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白三烯D4受体拮抗剂ONO-1078增强多药耐药细胞对长春新碱的敏感性。

Increased sensitivity to vincristine of MDR cells by the leukotriene D4 receptor antagonist, ONO-1078.

作者信息

Nagayama S, Chen Z S, Kitazono M, Takebayashi Y, Niwa K, Yamada K, Tani A, Haraguchi M, Sumizawa T, Furukawa T, Aikou T, Akiyama S

机构信息

The Institute for Cancer Research, Faculty of Medicine, Kagoshima University, Sakuragaoka, Japan.

出版信息

Cancer Lett. 1998 Aug 14;130(1-2):175-82. doi: 10.1016/s0304-3835(98)00132-3.

Abstract

The leukotriene D4 (LTD4) receptor antagonist, 4-oxo-8-[p-(4-phenylbutyloxy)benzoylamino]-2-(tetrazol-5-yl) -4H-1-benzopyran hemihydrate (ONO-1078) is used for the treatment of allergic asthma and other immediate hypersensitivity diseases. We examined the effect of ONO-1078 on the sensitivity to vincristine (VCR) of MRP overexpressing multidrug-resistant CV60 and its parental drug-sensitive KB-3-1 cell lines. The sensitivity to VCR of KB-3-1 and CV60 cells was increased 13- and 15-fold, respectively, by ONO-1078 at the maximum non-toxic concentration (100 microM). The VCR sensitivity of multidrug-resistant KB-C2 cells that overexpressed P-gp was increased 2.6-fold by ONO-1078. The accumulation of VCR in KB-3-1, CV60 and KB-C2 cells was significantly increased by ONO-1078. The efflux of VCR from KB-3-1 cells was not inhibited, but that from CV60 cells was enhanced compared with that from KB-3-1 cells and was partially inhibited by ONO-1078. ONO-1078 competitively inhibited the ATP-dependent [3H]LTC4 uptake in membrane vesicles isolated from CV60 cells. These findings suggest that ONO-1078 inhibits the transporting activity of MRP and that ONO-1078 increases the sensitivity to VCR of KB-3-1 cells by increasing the VCR uptake in the cells.

摘要

白三烯D4(LTD4)受体拮抗剂4-氧代-8-[对-(4-苯基丁氧基)苯甲酰氨基]-2-(四氮唑-5-基)-4H-1-苯并吡喃半水合物(ONO-1078)用于治疗过敏性哮喘和其他速发型超敏反应性疾病。我们研究了ONO-1078对多药耐药相关蛋白(MRP)过表达的多药耐药CV60细胞及其亲代药物敏感KB-3-1细胞系对长春新碱(VCR)敏感性的影响。在最大无毒浓度(100 microM)下,ONO-1078使KB-3-1和CV60细胞对VCR的敏感性分别提高了13倍和15倍。过表达P-糖蛋白(P-gp)的多药耐药KB-C2细胞对VCR的敏感性被ONO-1078提高了2.6倍。ONO-1078显著增加了VCR在KB-3-1、CV60和KB-C2细胞中的蓄积。KB-3-1细胞中VCR的外排未受抑制,但与KB-3-1细胞相比,CV60细胞中VCR的外排增强,且被ONO-1078部分抑制。ONO-1078竞争性抑制从CV60细胞分离的膜囊泡中ATP依赖的[3H]LTC4摄取。这些发现表明,ONO-1078抑制MRP的转运活性,并且ONO-1078通过增加细胞对VCR的摄取来提高KB-3-1细胞对VCR的敏感性。

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