Methanolic Extract of Costus pictus D. DON Induces Cytotoxicity in Liver Hepatocellular Carcinoma Cells Mediated by Histone Deacetylase Inhibition

被引:5
作者
Neethu, P. V. [1 ]
Suthindhiran, K. [1 ]
Jayasri, M. A. [1 ]
机构
[1] VIT Univ, Dept Biomed Sci, Marine Biotechnol & Bioprod Lab, Sch Biosci & Technol, Vellore, Tamil Nadu, India
关键词
Costus pictus methanolic extract; cytotoxicity; liver hepatocellular carcinoma cells; histone deacetylase; IN-VITRO; INSULIN-SECRETION; ANTIOXIDANT; ANTICANCER; PROLIFERATION; MECHANISMS;
D O I
10.4103/pm.pm_524_16
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Background: Leaves of Costus pictus D. Don, (insulin plant) are used as dietary supplement for the treatment of diabetes. Objective: The antidiabetic activity of this plant is well documented, but its activity on different cell types and mechanism remains unknown. Thus, the present study evaluates the cytotoxicity of C. pictus methanolic extract (CPME) against various cancer and normal cells. Materials and Methods: Dried leaves of C. pictus were extracted using methanol and were subjected to histone deacetylase (HDAC) inhibition and toxicity studies. Results: The CPME displayed a selective toxicity toward tested cancer cells in a dose-and time-dependent manner. CPME exhibited significant cytotoxicity on Liver hepatocellular carcinoma cells (Hep G2) (half maximal inhibitory concentration IC50 = 6.7 mu g/ml). Since CPME demonstrates both antidiabetic, anticancer activity, and HDAC enzyme play a detrimental role in both the complications, we have evaluated the CPME-induced HDAC regulation on Hep G2 cell lines. CPME showed a notable HDAC inhibition (55%). Furthermore, CPME did not show any genotoxicity or membrane instability at the tested concentrations. Conclusion: CPME demonstrates selective cytotoxicity toward tumor cells at a lower concentration through HDAC inhibition.
引用
收藏
页码:S533 / S538
页数:6
相关论文
共 42 条
[1]  
Akanji M. A., 2013, FOUNTAIN J NATURAL A, V2, P6
[2]   Costus Pictus Extracts Stimulate Insulin Secretion from Mouse and Human Islets of Langerhans In Vitro [J].
Al-Romaiyan, Altaf ;
Jayasri, Mangalam A. ;
Mathew, T. Lazar ;
Huang, Guo-Cai ;
Amiel, Stephanie ;
Jones, Peter M. ;
Persaud, Shanta J. .
CELLULAR PHYSIOLOGY AND BIOCHEMISTRY, 2010, 26 (06) :1051-1058
[3]   Next generation sequencing and de novo transcriptome analysis of Costus pictus D. Don, a non-model plant with potent anti-diabetic properties [J].
Annadurai, Ramasamy S. ;
Jayakumar, Vasanthan ;
Mugasimangalam, Raja C. ;
Katta, Mohan A. V. S. K. ;
Anand, Sanchita ;
Gopinathan, Sreeja ;
Sarma, Santosh Prasad ;
Fernandes, Sunjay Jude ;
Mullapudi, Nandita ;
Murugesan, S. ;
Rao, Sudha Narayana .
BMC GENOMICS, 2012, 13 :1-15
[4]   Histone deacetylase inhibitor BML-210 induces growth inhibition and apoptosis and regulates HDAC and DAPC complex expression levels in cervical cancer cells [J].
Borutinskaite, Veronika V. ;
Magnusson, Karl-Eric ;
Navakauskiene, Ruta .
MOLECULAR BIOLOGY REPORTS, 2012, 39 (12) :10179-10186
[5]   Histone deacetylase inhibitors: Mechanisms of cell death and promise in combination cancer therapy [J].
Carew, Jennifer S. ;
Giles, Francis J. ;
Nawrocki, Steffan T. .
CANCER LETTERS, 2008, 269 (01) :7-17
[6]   In Vitro α-Glucosidase Inhibition, Antioxidant, Anticancer, and Antimycobacterial Properties of Ethyl Acetate Extract of Aegle tamilnadensis Abdul Kader (Rutaceae) Leaf [J].
Chandran, Pratap R. ;
Kumar, Nishanth S. ;
Manju, S. ;
Kader, Abdul S. ;
Kumar, Dileep B. S. .
APPLIED BIOCHEMISTRY AND BIOTECHNOLOGY, 2015, 175 (02) :1247-1261
[7]  
Choudhary J., 2012, GREENHOUSE DESIGN CO, V2, P244
[8]   Histone Deacetylase (HDAC) Inhibition as a Novel Treatment for Diabetes Mellitus [J].
Christensen, Dan P. ;
Dahllof, Mattias ;
Lundh, Morten ;
Rasmussen, Daniel N. ;
Nielsen, Mette D. ;
Billestrup, Nils ;
Grunnet, Lars G. ;
Mandrup-Poulsen, Thomas .
MOLECULAR MEDICINE, 2011, 17 (5-6) :378-390
[9]   Histone deacetylase inhibitors from the rhizomes of Zingiber zerumbet [J].
Chung, Ill-Min ;
Kim, Min-Young ;
Park, Won-Hwan ;
Moon, Hyung-In .
PHARMAZIE, 2008, 63 (10) :774-776
[10]   METABOLIC DISEASE New role for HDACs in glucose homeostasis [J].
Crunkhorn, Sarah .
NATURE REVIEWS DRUG DISCOVERY, 2011, 10 (07) :493-493