Anti-proliferative activities of selected Chinese medicinal herbs against human cancer cell lines

The main objective of this study was to investigate the anti-proliferative properties of selected traditional Chinese medicinal herbs with a view to discover potential candidates for the isolation of anti-cancer compounds and also for designing new anti-cancer herbal formulations. The plants selected for this study have ethno pharmacological importance and currently used in Chinese medicine. The Methylthiazolyldiphenyltetrazolium bromide (MTT) assay was conducted to determine the anti-proliferative properties of the aqueous and ethanol extracts of the selected herbs against one control cell line and 5 human carcinoma cell lines. The key herbs found in this study that are expected to have excellent future potential are: Ligustrum lucidum, Paeonia suffuticosa, Sarcandra glabra, Scutellaria baicalensis, and Sanguisora officinalis. The study also indicated that the ethanol extracts of the selected herbs were generally more effective than the aqueous extracts. The findings of this study provide strong evidence that some of the medicinal plants examined are potential candidates for the isolation of anti-cancer compounds and also for designning new anti-cancer herbal formulations.

[1]  H. Wagner Immunomodulatory Agents from Plants , 2012, Progress in Inflammation Research.

[2]  Yan Chen,et al.  Identification of Two Polysaccharides from Prunella vulgaris L. and Evaluation on Their Anti-Lung Adenocarcinoma Activity , 2010, Molecules.

[3]  W. Cho Supportive Cancer Care with Chinese Medicine , 2009 .

[4]  D. Newman,et al.  Impact of natural products on developing new anti-cancer agents. , 2009, Chemical reviews.

[5]  Zhongjun Ma,et al.  Cytotoxicity of Chinese motherwort (YiMuCao) aqueous ethanol extract is non-apoptotic and estrogen receptor independent on human breast cancer cells. , 2009, Journal of ethnopharmacology.

[6]  Likun Gong,et al.  Comparative 28-day repeated oral toxicity of Longdan Xieganwan, Akebia trifoliate (Thunb.) koidz., Akebia quinata (Thunb.) Decne. and Caulis aristolochiae manshuriensis in mice. , 2008, Journal of ethnopharmacology.

[7]  D. Newman,et al.  Natural products as sources of new drugs over the last 25 years. , 2007, Journal of natural products.

[8]  K. Kang,et al.  Antioxidative effects of quercetin-glycosides isolated from the flower buds of Tussilago farfara L. , 2006, Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association.

[9]  John A Timbrell,et al.  In vitro cytotoxicity assays: comparison of LDH, neutral red, MTT and protein assay in hepatoma cell lines following exposure to cadmium chloride. , 2006, Toxicology letters.

[10]  M. Campbell,et al.  In vitro anticancer activity of twelve Chinese medicinal herbs , 2005, Phytotherapy research : PTR.

[11]  L. Yi,et al.  Calorimetric investigation of the effect of hydroxyanthraquinones in Rheum officinale Baill on Staphylococcus aureus growth , 2005 .

[12]  F. Koehn,et al.  The evolving role of natural products in drug discovery , 2005, Nature Reviews Drug Discovery.

[13]  S. Jo,et al.  Anti-metastatic activity of Acanthopanax senticosus extract and its possible immunological mechanism of action. , 2004, Journal of ethnopharmacology.

[14]  R. Ajayakumar Anticancer and immunostimulatory compounds from Andrographis paniculata , 2004 .

[15]  Ping Liu,et al.  A self-learning expert system for diagnosis in traditional Chinese medicine , 2004, Expert Syst. Appl..

[16]  B. Suresh,et al.  Antitumor activity of total alkaloid fraction of solanum pseudocapsicum leaves , 2003, Phytotherapy research : PTR.

[17]  Zhengtao Wang,et al.  Antioxidant activity of compounds from the medicinal herb Aster tataricus. , 2003, Comparative biochemistry and physiology. Toxicology & pharmacology : CBP.

[18]  M. López-Lázaro,et al.  Cytotoxic effect of Plantago spp. on cancer cell lines. , 2003, Journal of ethnopharmacology.

[19]  C. Takimoto Anticancer drug development at the US National Cancer Institute , 2003, Cancer Chemotherapy and Pharmacology.

[20]  Tomoaki Tanaka,et al.  Isolation of (+)-Catechin and (-)-Epicatechin from Actinidia arguta as Bone Marrow Cell Proliferation Promoting Compounds , 2003, Planta medica.

[21]  K. Chai,et al.  Inhibitory effects of methanol extract of Cyperus rotundus rhizomes on nitric oxide and superoxide productions by murine macrophage cell line, RAW 264.7 cells. , 2001, Journal of ethnopharmacology.

[22]  S. Nayak In vitro multiplication and microrhizome induction in Curcuma aromatica Salisb. , 2000, Plant Growth Regulation.

[23]  H. Kim,et al.  The nitric oxide-producing properties of Solanum lyratum. , 1999, Journal of ethnopharmacology.

[24]  J. Hancke,et al.  Schisandra chinensis (Turcz.) Baill , 1999 .

[25]  E. Park,et al.  Licochalcone A: An Inducer of Cell Differentiation and Cytotoxic Agent from Pogostemon cabling 1 , 1998, Planta medica.

[26]  G. Cordell,et al.  Can ethnopharmacology contribute to the development of new anticancer drugs? , 1991, Journal of ethnopharmacology.

[27]  Andrew O. Martinez,et al.  A rapid and simple MTT-based spectrophotometric assay for determining drug sensitivity in monolayer cultures , 1988 .

[28]  G. Franz UNTERSUCHUNGEN ÜBER DIE SCHLEIMPOLYSACCHARIDE VON TUSSILAGO FARFARA L., SYMPHYTUM OFFICINALIS L., BORAGO OFFICINALIS L. UND VIOLA TRICOLOR L. , 1969, Planta medica.

[29]  Shakhnoza S. Azimova,et al.  Borago officinalis L. , 2012 .

[30]  Z. Tian,et al.  Diarylheptanoids from the rhizomes of Alpinia officinarum and their anticancer activity. , 2008, Fitoterapia.

[31]  Z. Liao,et al.  Antioxidative flavanone glycosides from the branches and leaves of Viscum coloratum. , 2006, Chemical & pharmaceutical bulletin.

[32]  Chin-Yuan Hsu Antioxidant activity of extract from Polygonum aviculare L. , 2006, Biological research.

[33]  F. Peláez,et al.  In vitro antitumor structure-activity relationships of threo/trans/threo/trans/erythro bis-tetrahydrofuranic acetogenins: correlations with their inhibition of mitochondrial complex I. , 2005, Oncology research.

[34]  P. Cox The ethnobotanical approach to drug discovery: strengths and limitations. , 1994, Ciba Foundation symposium.