Evaluation of anthraquinones from Himalayan rhubarb (Rheum emodi Wall. ex Meissn.) as antiproliferative agents

被引:37
作者
Pandith, Shahzad A. [1 ]
Hussain, Aashiq [2 ]
Bhat, Wajid Waheed [1 ]
Dhar, Niha [1 ]
Qazi, Asif Khurshid [2 ]
Rana, Satiander [1 ]
Razdan, Sumeer [1 ]
Wani, Tareq A. [3 ]
Shah, Manzoor A. [4 ]
Bedi, Y. S. [1 ]
Hamid, Abid [2 ]
Lattoo, Surrinder K. [1 ]
机构
[1] CSIR, Indian Inst Integrat Med, Jammu 180001, India
[2] CSIR, Indian Inst Integrat Med, Canc Pharmacol Div, Jammu 180001, India
[3] CSIR, Indian Inst Integrat Med, Genet Resources & Agrotechnol Div, Jammu 180001, India
[4] Univ Kashmir, Dept Bot, Srinagar 190006, Jammu & Kashmir, India
关键词
Rheum emodi; HPLC; Anthraquinones; MTT assay; MMP loss; Cell cycle; APOPTOSIS; CANCER; CELLS; INDUCTION; EXTRACT;
D O I
10.1016/j.sajb.2014.07.012
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Rheum emodi (Polygonaceae), a multipurpose medicinal herb is a rich repository of pharmacologically active secondary metabolites known as anthraquinones. The present study entails HPLC quantitation and in vitro activity of four major constituents and the extracts of R. emodi. The anthraquinone glycosides were more abundant than their aglycone constituents viz. emodin and chrysophanol. MTT assay was used to assess the in vitro antiproliferative activity of anthraquinones and extracts on four cancer cell lines namely MIAPaCa-2, HCT-116, MCF-7 and T47D. The cytotoxicity was more obvious on MIAPaCa-2. Further, the study of mechanism of action involving cell cycle analysis and determination of mitochondrial membrane potential (MMP) loss was also investigated. The extracts significantly reduced cell viability by inducing apoptosis/necrosis and cell cycle arrest with concurrent loss of MMP (Delta psi m) in a concentration dependent manner. The methanolic extract of rhizome (SPL5) with the least IC50 value (25 mu g/ml) showed a significant increase-in the percentage of apoptotic/necrotic cells (42.3% at 100 mu g/ml) compared to that of vehicle treated cells (11.6%). These cellular manifestations corresponded remarkably with a decrease in the integrity of the mitochondrial membrane. In conclusion, SPL5 with emodin and chrysophanol as the preponderant constituents exhibited considerable antiproliferative activity possibly by reducing cell viability and stirring up Aim loss. (C) 2014 SAAB. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 8
页数:8
相关论文
共 20 条
[1]  
Abdullaev F, 2001, PHARMACOLOGY AND THERAPEUTICS IN THE NEW MILLENNIUM, P345
[2]   Anticancer potential of Himalayan plants [J].
Bhatia, Anjana ;
Arora, Saroj ;
Singh, Bikram ;
Kaur, Gurveen ;
Nagpal, Avinash .
PHYTOCHEMISTRY REVIEWS, 2011, 10 (03) :309-323
[3]   ELEVATIONAL VARIATION OF QUINOLIZIDINE ALKALOID CONTENTS IN A LUPINE (LUPINUS-ARGENTEUS) OF THE ROCKY-MOUNTAINS [J].
CAREY, DB ;
WINK, M .
JOURNAL OF CHEMICAL ECOLOGY, 1994, 20 (04) :849-857
[4]   Apoptosis and non-apoptotic deaths in cancer development and treatment response [J].
de Bruin, Elza C. ;
Mederna, Jan Paul .
CANCER TREATMENT REVIEWS, 2008, 34 (08) :737-749
[5]   Altitudinal variability in anthraquinone constituents from novel cytotypes of Rumex nepalensis Spreng-a high value medicinal herb of North Western Himalayas [J].
Farooq, Umer ;
Pandith, Shahzad A. ;
Saggoo, Manjit Inder Singh ;
Lattoo, Surrinder K. .
INDUSTRIAL CROPS AND PRODUCTS, 2013, 50 :112-117
[6]   Novel curcumin- and emodin-related compounds identified by in silico 2D/3D conformer screening induce apoptosis in tumor cells -: art. no. 97 [J].
Füllbeck, M ;
Huang, XH ;
Dumdey, R ;
Frommel, C ;
Dubiel, W ;
Preissner, R .
BMC CANCER, 2005, 5 (1)
[7]   Antioxidant and antiproliferative activities of Abrus precatorius leaf extracts - an in vitro study [J].
Gul, Mir Z. ;
Ahmad, Farhan ;
Kondapi, Anand K. ;
Qureshi, Insaf A. ;
Ghazi, Irfan A. .
BMC COMPLEMENTARY AND ALTERNATIVE MEDICINE, 2013, 13
[8]   Analysis of mortality rates for pancreatic cancer across the world [J].
Hariharan, D. ;
Saied, A. ;
Kocher, H. M. .
HPB, 2008, 10 (01) :58-62
[9]   Inhibitory effect of emodin on tumor invasion through suppression of activator protein-1 and nuclear factor-κB [J].
Huang, Q ;
Shen, HM ;
Ong, CN .
BIOCHEMICAL PHARMACOLOGY, 2004, 68 (02) :361-371
[10]   Pancreatic cancer [J].
Li, DH ;
Xie, KP ;
Wolff, R ;
Abbruzzese, JL .
LANCET, 2004, 363 (9414) :1049-1057