Natural lignans from Arctium lappa modulate P-glycoprotein efflux function in multidrug resistant cancer cells

被引:65
作者
Su, Shan [1 ]
Cheng, Xinlai [1 ]
Wink, Michael [1 ]
机构
[1] Heidelberg Univ, Inst Pharm & Mol Biotechnol, D-69120 Heidelberg, Germany
关键词
Arctium lappa; Cancer cells; Lignans; Multidrug resistance; P-glycoprotein; ARCTIGENIN ENHANCES CHEMOSENSITIVITY; PLANT SECONDARY METABOLITES; DIGITONIN; EXPRESSION; INHIBITION; CISPLATIN; SYNERGISM; VERAPAMIL;
D O I
10.1016/j.phymed.2014.12.009
中图分类号
Q94 [植物学];
学科分类号
071001 [植物学];
摘要
Arctium lappa is a well-known traditional medicinal plant in China (TCM) and Europe that has been used for thousands of years to treat arthritis, baldness or cancer. The plant produces lignans as secondary metabolites which have a wide range of bioactivities. Yet, their ability to reverse multidrug resistance (MDR) in cancer cells has not been explored. In this study, we isolated six lignans from A. lappa seeds, namely arctigenin, matairesinol, arctiin, (iso)lappaol A, lappaol C, and lappaol F. The MDR reversal potential of the isolated lignans and the underlying mechanism of action were studied using two MDR cancer cell lines, CaCo2 and CEM/ADR 5000 which overexpress P-gp and other ABC transporters. In two-drug combinations of lignans with the cytotoxic doxorubicin, all lignans exhibited synergistic effects in CaCo2 cells and matairesinol, arctiin, lappaol C and lappaol F display synergistic activity in CEM/ADR 5000 cells. Additionally, in three-drug combinations of lignans with the saponin digitonin and doxorubicin MDR reversal activity was even stronger enhanced. The lignans can increase the retention of the P-gp substrate rhodamine 123 in CEM/ADR 5000 cells, indicating that lignans can inhibit the activity of P-gp. Our study provides a first insight into the potential chemosensitizing activity of a series of natural lignans, which might be candidates for developing novel adjuvant anticancer agents. (C) 2015 Elsevier GmbH. All rights reserved.
引用
收藏
页码:301 / 307
页数:7
相关论文
共 29 条
[1]
Biochemical, cellular, and pharmacological aspects of the multidrug transporter [J].
Ambudkar, SV ;
Dey, S ;
Hrycyna, CA ;
Ramachandra, M ;
Pastan, I ;
Gottesman, MM .
ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 1999, 39 :361-398
[2]
Modulation of P-glycoprotein expression and function by curcumin in multidrug-resistant human KB cells [J].
Anuchapreeda, S ;
Leechanachai, P ;
Smith, MM ;
Ambudkar, SV ;
Limtrakul, P .
BIOCHEMICAL PHARMACOLOGY, 2002, 64 (04) :573-582
[3]
Identification of arctigenin as an antitumor agent having the ability to eliminate the tolerance of cancer cells to nutrient starvation [J].
Awale, S ;
Lu, J ;
Kalauni, SK ;
Kurashima, Y ;
Tezuka, Y ;
Kadota, S ;
Esumi, H .
CANCER RESEARCH, 2006, 66 (03) :1751-1757
[4]
Theoretical basis, experimental design, and computerized simulation of synergism and antagonism in drug combination studies [J].
Chou, Ting-Chao .
PHARMACOLOGICAL REVIEWS, 2006, 58 (03) :621-681
[5]
Activity of drugs from traditional Chinese medicine toward sensitive and MDR1- or MRP1-overexpressing multidrug-resistant human CCRF-CEM leukemia cells [J].
Efferth, T ;
Davey, M ;
Olbrich, A ;
Rücker, G ;
Gebhart, E ;
Davey, R .
BLOOD CELLS MOLECULES AND DISEASES, 2002, 28 (02) :160-168
[6]
Synergism of three-drug combinations of sanguinarine and other plant secondary metabolites with digitonin and doxorubicin in multi-drug resistant cancer cells [J].
Eid, Safaa Yehia ;
El-Readi, Mahmoud Zaki ;
Wink, Michael .
PHYTOMEDICINE, 2012, 19 (14) :1288-1297
[7]
Digitonin synergistically enhances the cytotoxicity of plant secondary metabolites in cancer cells [J].
Eid, Safaa Yehia ;
El-Readi, Mahmoud Zaki ;
Wink, Michael .
PHYTOMEDICINE, 2012, 19 (14) :1307-1314
[8]
Inhibition of P-glycoprotein activity by limonin and other secondary metabolites from Citrus species in human colon and leukaemia cell lines [J].
El-Readi, Mahmoud Zaki ;
Hamdan, Dalia ;
Farrag, Nawal ;
El-Shazly, Assem ;
Wink, Michael .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2010, 626 (2-3) :139-145
[9]
THE CYTOSKELETON OF DIGITONIN-TREATED RAT HEPATOCYTES [J].
FISKUM, G ;
CRAIG, SW ;
DECKER, GL ;
LEHNINGER, AL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1980, 77 (06) :3430-3434
[10]
EXPLOITING MULTIDRUG-RESISTANCE TO TREAT CANCER [J].
GOTTESMAN, MM ;
AMBUDKAR, SV ;
NI, B ;
ARAN, JM ;
SUGIMOTO, Y ;
CARDARELLI, CO ;
PASTAN, I .
COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY, 1994, 59 :677-683