• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

人U-937淋巴瘤细胞系中长春新碱耐药性的产生以及对环孢素A和维拉帕米敏感性的增加,且不存在170-kDa P-糖蛋白的过表达。

Development of vincristine resistance and increased sensitivity to cyclosporin A and verapamil in the human U-937 lymphoma cell line without overexpression of the 170-kDa P-glycoprotein.

作者信息

Botling J, Liminga G, Larsson R, Nygren P, Nilsson K

机构信息

Department of Pathology, University Hospital, Uppsala University, Sweden.

出版信息

Int J Cancer. 1994 Jul 15;58(2):269-74. doi: 10.1002/ijc.2910580221.

DOI:10.1002/ijc.2910580221
PMID:7913083
Abstract

A vincristine (Vcr)-resistant subline of the human histiocytic lymphoma cell line U-937 (U-937-vcr) has been established and characterized with respect to its phenotypic features, including growth rate, surface marker expression and ability to respond to differentiation-inducing agents. The sensitivity of U-937-vcr cells to the direct cytotoxicity of cyclosporin A (CsA) and verapamil (Ver), and the capacity of these drugs to modify Vcr resistance, were also examined. The U-937-vcr cells exhibited a more than 200-fold resistance to Vcr, and cross-resistance to vinorelbin and taxol. Also, there was a slight cross-resistance to colchicine, doxorubicin and VP16. However, the response of U-937-vcr to CsA or Ver alone was substantially altered, with a marked decrease in their respective IC50s. The U-937-vcr cells did not show increased levels of pgp 170. We conclude that the development of Vcr resistance was not associated with a change in the major phenotypic properties of the U-937 cell line, and that resistance modifier hypersensitivity was not associated with increase in pgp 170 expression.

摘要

已建立人组织细胞淋巴瘤细胞系U - 937的长春新碱(Vcr)耐药亚系(U - 937 - vcr),并对其表型特征进行了鉴定,包括生长速率、表面标志物表达以及对诱导分化剂的反应能力。还检测了U - 937 - vcr细胞对环孢素A(CsA)和维拉帕米(Ver)直接细胞毒性的敏感性,以及这些药物改变Vcr耐药性的能力。U - 937 - vcr细胞对Vcr表现出200多倍的耐药性,对长春瑞滨和紫杉醇存在交叉耐药性。此外,对秋水仙碱、阿霉素和VP16有轻微交叉耐药性。然而,U - 937 - vcr对单独的CsA或Ver的反应有显著改变,其各自的半数抑制浓度(IC50)明显降低。U - 937 - vcr细胞未显示P -糖蛋白170(pgp 170)水平升高。我们得出结论,Vcr耐药性的产生与U - 937细胞系主要表型特性的改变无关,耐药性调节剂超敏反应与pgp 170表达增加无关。

相似文献

1
Development of vincristine resistance and increased sensitivity to cyclosporin A and verapamil in the human U-937 lymphoma cell line without overexpression of the 170-kDa P-glycoprotein.人U-937淋巴瘤细胞系中长春新碱耐药性的产生以及对环孢素A和维拉帕米敏感性的增加,且不存在170-kDa P-糖蛋白的过表达。
Int J Cancer. 1994 Jul 15;58(2):269-74. doi: 10.1002/ijc.2910580221.
2
A non-P-glycoprotein-mediated mechanism of vincristine transport which is affected by resistance modifiers and present in chemosensitive cells.一种非P-糖蛋白介导的长春新碱转运机制,该机制受耐药调节剂影响且存在于化疗敏感细胞中。
Leukemia. 1994 Jun;8(6):985-9.
3
Ascorbic acid increases drug accumulation and reverses vincristine resistance of human non-small-cell lung-cancer cells.抗坏血酸可增加药物蓄积,并逆转人非小细胞肺癌细胞对长春新碱的耐药性。
Biochem J. 1994 Aug 1;301 ( Pt 3)(Pt 3):759-64. doi: 10.1042/bj3010759.
4
Effect of MDR antagonists on the cidal activity of vincristine for cells expressing MDR-1 is superior to those expressing MRP.
Int J Oncol. 1998 Aug;13(2):343-8. doi: 10.3892/ijo.13.2.343.
5
Differential in vitro sensitivity of human tumor and normal cells to chemotherapeutic agents and resistance modulators.人类肿瘤细胞与正常细胞对化疗药物及耐药调节剂的体外敏感性差异
Int J Cancer. 1991 Jun 19;48(4):598-604. doi: 10.1002/ijc.2910480419.
6
Reversal of multidrug resistance by an immunosuppressive agent FK-506.
Cancer Chemother Pharmacol. 1992;29(3):195-200. doi: 10.1007/BF00686252.
7
[The efflux of intracellular vincristine in drug-resistant human lung cancer cells is not mediated by P-glycoprotein].[耐药性人肺癌细胞内长春新碱的外排并非由P-糖蛋白介导]
J Formos Med Assoc. 1993 Jun;92 Suppl 2:S69-75.
8
Modulator activity of PSC 833 and cyclosporin-A in vincristine and doxorubicin-selected multidrug resistant murine leukemic cells.PSC 833和环孢素A对长春新碱和阿霉素筛选的多药耐药小鼠白血病细胞的调节活性
Leuk Res. 2001 Jan;25(1):85-93. doi: 10.1016/s0145-2126(00)00094-1.
9
Verapamil and cyclosporin A sensitize human kidney tumor cells to vincristine in absence of membrane P-glycoprotein and without apparent changes in the cytoplasmic free Ca2+ concentration.维拉帕米和环孢素A在不存在膜P-糖蛋白且细胞质游离钙离子浓度无明显变化的情况下,使人类肾肿瘤细胞对长春新碱敏感。
Biosci Rep. 1990 Apr;10(2):231-7. doi: 10.1007/BF01116583.
10
Effects of amiodarone, cyclosporin A, and PSC 833 on the cytotoxicity of mitoxantrone, doxorubicin, and vincristine in non-P-glycoprotein human small cell lung cancer cell lines.胺碘酮、环孢素A和PSC 833对非P-糖蛋白人小细胞肺癌细胞系中米托蒽醌、阿霉素和长春新碱细胞毒性的影响。
Cancer Res. 1994 Oct 15;54(20):5368-73.

引用本文的文献

1
Screening for phenotype selective activity in multidrug resistant cells identifies a novel tubulin active agent insensitive to common forms of cancer drug resistance.在多药耐药细胞中筛选表型选择性活性,鉴定出一种新型微管活性药物,对常见形式的癌症耐药性不敏感。
BMC Cancer. 2013 Aug 6;13:374. doi: 10.1186/1471-2407-13-374.
2
Nanoparticulate Quillaja saponin induces apoptosis in human leukemia cell lines with a high therapeutic index.纳米颗粒 Quillaja saponin 诱导高治疗指数的人白血病细胞系凋亡。
Int J Nanomedicine. 2010 Feb 2;5:51-62.
3
Naturally occurring resistance of bone marrow mononuclear and metastatic cancer cells to anticancer agents.
骨髓单核细胞和转移性癌细胞对抗癌药物的天然耐药性。
Clin Exp Metastasis. 2006;23(5-6):249-58. doi: 10.1007/s10585-006-9034-x. Epub 2006 Nov 3.
4
Identification of molecular mechanisms for cellular drug resistance by combining drug activity and gene expression profiles.通过结合药物活性和基因表达谱来鉴定细胞耐药性的分子机制。
Br J Cancer. 2005 Aug 22;93(4):483-92. doi: 10.1038/sj.bjc.6602699.
5
Comparison of the cytotoxic activity of melphalan with L-prolyl-m-L-sarcolysyl-L-p-fluorophenylalanine in human tumour cell lines and primary cultures of tumour cells from patients.美法仑与L-脯氨酰-m-L-肌氨酸-L-对氟苯丙氨酸在人肿瘤细胞系及患者肿瘤细胞原代培养物中的细胞毒性活性比较。
Br J Cancer. 1998 Aug;78(3):328-35. doi: 10.1038/bjc.1998.494.
6
Cytotoxic activity of topotecan in human tumour cell lines and primary cultures of human tumour cells from patients.拓扑替康对人肿瘤细胞系及患者来源的人肿瘤细胞原代培养物的细胞毒活性。
Br J Cancer. 1997;76(2):211-9. doi: 10.1038/bjc.1997.364.
7
Anti-cancer drug characterisation using a human cell line panel representing defined types of drug resistance.使用代表特定耐药类型的人类细胞系面板对抗癌药物进行表征。
Br J Cancer. 1996 Sep;74(6):888-96. doi: 10.1038/bjc.1996.453.
8
Multidrug resistance-associated protein-mediated multidrug resistance modulated by cyclosporin A in a human bladder cancer cell line.环孢菌素A对人膀胱癌细胞系中多药耐药相关蛋白介导的多药耐药的调节作用
Jpn J Cancer Res. 1995 Oct;86(10):969-77. doi: 10.1111/j.1349-7006.1995.tb03009.x.