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氧化苦参碱和粉防己碱对鼻咽癌耐药细胞株的耐药逆转作用 被引量:10

Reversal effect of oxymatrine and tetrandrine on multidrug resistance in HNE-1(200)cell line
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摘要 目的:研究天然有效成分氧化苦参碱(Oxy)和粉防己碱(TET)对鼻咽癌耐药细胞株HNE-1(200)的耐药逆转作用.方法:以鼻咽癌耐药细胞株HNE-1(200)为研究对象,用MTT法测定无毒剂量的Oxy和TET作用后HNE-1(200)耐药细胞对常用抗肿瘤药物顺铂(DDP),5-氟尿嘧啶(5-Fu),长春新碱(vincristine,VCR),阿霉素(Adriamycin,ADM)的增殖抑制率和IC50,并进一步计算其逆转指数.结果:无毒剂量的TET和Oxy分别与4种抗肿瘤药物联合应用后,抗肿瘤药物对耐药细胞的增殖抑制率增加.TET逆转HNE-1(200)细胞对DDP,5-Fu,VCR,ADM的耐药指数分别为2.25,2.1,3.19,2.27;Oxy逆转HNE-1(200)细胞对DDP,5-Fu,VCR,ADM的耐药指数分别为1.59,1.26,2.28,1.26.结论:低毒浓度的天然药物Oxy和TET对鼻咽耐药细胞株HNE-1(200)具有一定的耐药逆转作用. AIM: To study the reversal effects of natural substances oxymatrine and tetrandrine on multidrug resistance in human nasopharyngeal carcinoma muhidrug resistance HNE-1 (200) cell line. METHODS: Human nasopharyngeal carcinoma multidrug resistance HNE-1 (:200) cell line was used as the subject. MTt reduction assay was used to investigate the drug interaction of oxymatrine, tetrandrine, cisplatin ( DDP), 5-Fluorouracil ( 5-Fu ), vincristine(VCR) and adriamycin ( ADM ) on HNE-1 ( 200 ) cell line. IC50 and RI were detected. RESULTS: After non-toxic dose of tetrandrine was interacted with DDP, 5-Fu, VCR and ADM, the cell inhibition rate of the four drugs increased. The resistance index (RI) of tetandrine with DDP, 5-Fu, VCR and ADM was 2.25, 2. 1, 3. 19 and 2.27 respectively. The RI of oxymatrine with DDP, 5-Fu, VCR and ADM was 1.59, 1.26, 2.28 and 1.26 respectively. CONCLUSION: Oxymatrine and tetrandrine can reverse the muhidrug resistance of HNE-1 (200) cell line to DDP, 5-Fu, VCR and ADM.
出处 《第四军医大学学报》 北大核心 2009年第11期967-970,共4页 Journal of the Fourth Military Medical University
基金 重庆市卫生局中医处资助课题(渝中医[2003]32号2003-B-90)
关键词 氧化苦参碱 粉防己碱 鼻咽肿瘤 HNE-1(200)细胞系 多药耐药 oxymatrine tetrandrine nasopharyngeal neoplasms HNE-1 ( 200 ) cell line multidrug resistance
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  • 1Geromin D, Bourge JF, Soulie A, et al. Glycoprotein 170 induces platelet-activating factor receptor membrane expression and confers tumor cell hypersensitivity to NK-dependent cell lysis [ J ]. J Immunol, 2004,172(6) :3604 -3611. 被引量:1
  • 2Szabo D, Keyzer H, Kaiser HE, et al. Reversal of muhidrug resistance of tumor cells [ J ]. Anticancer Res, 2000,20 ( 6B ) : 4261 -4274. 被引量:1
  • 3罗文纪,虞荣喜,朱宁希.苦参碱诱导白血病细胞株HL-60分化的实验研究[J].中国医药学报,2001,16(5):21-24. 被引量:21
  • 4罗明,贺平,吴孟超,李琳芳,郭亚军.苦参碱和氧化苦参碱对二乙基亚硝胺诱发大鼠肝癌作用的影响[J].中国药理学通报,2000,16(4):416-417. 被引量:34
  • 5Keli SO, Hertog MGL, Feskens EJM, et al. Dietary flavonoids, antioxidant vitamins, and incidence of stroke [ J ]. Arch Intern Med, 1996,15 (6) :637 - 642. 被引量:1
  • 6He QY, Meng FH, Zhang HQ, et al. Reduction of dox or ubicire resistance by tetrandrine and duaricinenarring to nine resistant human leukemia(HU) cells[ J]. Acta Pharm Cologiccinica, 1996, 17(2) :17. 被引量:1
  • 7许文林,敖忠芳,陈玉心,盛瑞兰,夏薇,徐大为,朱广荣.汉防已甲素对柔红霉素和长春新碱增效作用的实验研究[J].中华血液学杂志,1994,15(5):256-257. 被引量:49
  • 8Hoffmeyer S, Burk O, van Richter O, et al. Functional polymorphisms of the human muhidrug-resistance gene: Multiple sequence variations and correlation of one allele with P-glycoprotein expression and activity in vivo[J]. Proc Natl Acad Sci USA, 2000,97(7) : 3473 -3478. 被引量:1
  • 9Fischer V, Rodriguez-Gascon A, Heitz F, et al. The multidrug resistance modulator valspodar( PSC 833 ) is metabolized by human cytochrome P450 3A: Implications for drug-drug interactions and pharmacological activity of the main metabolite [ J ]. Drug Metab Dispos, 1998,2(6) :802 -811. 被引量:1
  • 10Kim SE, Kim YH, Kim YC, et al. Torilin, a sesquiterpene from Torilis japonica, reverses multidrug-resistance in cancer cells[ J]. Planta Med, 1998,64(4) :332 -334. 被引量:1

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