Prediction of broad spectrum resistance of tumors towards anticancer drugs
Efferth, Thomas ; Konkimalla, V. Badireenath ; Wang, Yi-Fen ; Sauerbrey, Axel ; Meinhardt, Silke ; Zintl, Felix ; Mattern, Juegen ; Volm, Manfred
刊名CLINICAL CANCER RESEARCH
2008
卷号14期号:8页码:2405-2412
关键词TRADITIONAL CHINESE MEDICINE CASSETTE TRANSPORTER GENES SHORT-TERM TEST MULTIDRUG-RESISTANCE CELL-LINES CANCER-CHEMOTHERAPY TETRAZOLIUM ASSAY SENSITIVITY LEUKEMIA CYTOTOXICITY
ISSN号1078-0432
通讯作者Efferth, T (reprint author), German Canc Res Ctr, Neuenheimer Feld 280, D-69120 Heidelberg, Germany. t.efferth@dkfz.de
英文摘要Purpose: Drug resistance is a major obstacle in cancer chemotherapy. Although the statistical probability of therapeutic success is known for larger patient groups from clinical therapy trials, it is difficult to predict the individual response of tumors. The concept of individualized therapy aims to determine in vitro the drug response of tumors beforehand to choose effective treatment options for each individual patient. Experimental Design: We analyzed the cross-resistance profiles of different tumor types (cancers of lung, breast, and colon, and leukemia) towards drugs from different classes (anthracyclines, antibiotics, Vinca alkaloids, epipodophyllotoxins, antimetabolites, and alkylating agents) by nucleotide incorporation and 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assays. Hierarchical cluster analysis and COMPARE analyses were applied. Results: Tumors exert broad resistance profiles, e.g., tumors resistant to one drug tend to also be resistant to other drugs, whereas sensitive tumors reveal sensitivity towards many drugs. Interestingly, the broad spectrum resistance phenotype could reliably be predicted by doxorubicin alone. Expression of the ATP-binding cassette transporter P-glycoprotein (ABCB1, MDR1) and the proliferative activity of tumors were identified as underlying mechanisms of broad spectrum resistance. To find novel compounds with activity against drug-resistant tumors, a database with 2,420 natural products was screened for compounds acting independent of P-glycoprotein and the proliferative state of tumor cells. Conclusions: umors exert cross-resistance profiles much broader than the classical multidrug resistance phenotype. Broad spectrum resistance can be predicted by doxorubicin due to the multifactorial mode of action of this drug. Novel cytotoxic compunds from natural resources might be valuable tools for strategies to bypass broad spectrum resistance.
学科主题Oncology
收录类别SCI
语种英语
公开日期2012-10-12
内容类型期刊论文
源URL[http://ir.kib.ac.cn/handle/151853/15388]  
专题昆明植物研究所_植物化学与西部植物资源持续利用国家重点实验室
推荐引用方式
GB/T 7714
Efferth, Thomas,Konkimalla, V. Badireenath,Wang, Yi-Fen,et al. Prediction of broad spectrum resistance of tumors towards anticancer drugs[J]. CLINICAL CANCER RESEARCH,2008,14(8):2405-2412.
APA Efferth, Thomas.,Konkimalla, V. Badireenath.,Wang, Yi-Fen.,Sauerbrey, Axel.,Meinhardt, Silke.,...&Volm, Manfred.(2008).Prediction of broad spectrum resistance of tumors towards anticancer drugs.CLINICAL CANCER RESEARCH,14(8),2405-2412.
MLA Efferth, Thomas,et al."Prediction of broad spectrum resistance of tumors towards anticancer drugs".CLINICAL CANCER RESEARCH 14.8(2008):2405-2412.
个性服务
查看访问统计
相关权益政策
暂无数据
收藏/分享
所有评论 (0)
暂无评论
 

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。


©版权所有 ©2017 CSpace - Powered by CSpace