Planta Med 2006; 72(9): 862-864
DOI: 10.1055/s-2006-947165
Letter
© Georg Thieme Verlag KG Stuttgart · New York

Activity-Guided Isolation of Scopoletin and Isoscopoletin, the Inhibitory Active Principles towards CCRF-CEM Leukaemia Cells and Multi-Drug Resistant CEM/ADR5000 Cells, from Artemisia argyi

Michael Adams1 , Thomas Efferth2 , Rudolf Bauer1
  • 1Institute of Pharmaceutical Sciences, Department of Pharmacognosy, University of Graz, Graz, Austria
  • 2German Cancer Research Centre, Heidelberg, Germany
Further Information

Publication History

Received: October 11, 2005

Accepted: April 25, 2006

Publication Date:
21 June 2006 (online)

Abstract

The ethyl acetate extract of Artemisia argyi leaves showed substantial inhibition in a cell proliferation assay using human CCRF-CEM leukaemia cells. Bioassay-guided fractionation of the extract led to the isolation of scopoletin and isoscopoletin as the active principles. Their IC50 values were 2.6 and 4.0 μM, respectively. Additionally the two substances were tested against the multidrug resistant subline, CEM/ADR5000 where they both showed IC50 values of 1.6 μM. In contrast to the standard cytostatic drugs doxorubicin, vincristine, and paclitaxel, CEM/ADR5000 cells therefore did not exhibit cross-resistance to scopoletin and isoscopoletin.

References

  • 1 Pharmacopoeia of the Peoples Republic of China (English Edition). Beijing; Chemical Industry Press 2000: p 73
  • 2 Tang W, Eisenbrand G. Chinese drugs of plant origin: chemistry, pharmacology, and use in traditional and modern medicine. Berlin/Heidelberg; Springer Verlag 1992: p 175-8
  • 3 Efferth T, Davey M, Olbrich A, Ruecker G, Gebhart E, Davey R. Activity of drugs from traditional Chinese medicine toward sensitive and MDR1- or MRP1-overexpressing multidrug-resistant human CCRF-CEM leukaemia cells.  Blood Cells Mol Dis. 2002;  28 160-8
  • 4 Efferth T, Dunstan H, Sauerbrey A, Miyachi H, Chitambar C R. The antimalarial artesunate is also a potent anticancer drug.  Int J Oncol. 2001;  18 767-73
  • 5 Efferth T, Sauerbrey A, Olbrich A, Gebhart E, Rauch P, Weber H O. et al . Molecular modes of action of artesunate in tumour cell lines.  Mol Pharmacol. 2003;  64 382-94
  • 6 Kim K H, Jung D J, Min T J, Park S W. Cytotoxicity of Artemisia argyi extract against h9 (ATCC HTB 176) cell and antioxidant enzyme activities.  Yakhak Hoechi. 1999;  43 598-605
  • 7 Lee S H, Kim H K, Seo J M, Kang H M, Kim J H, Son K H. et al . Arteminolides B, C, and D, new inhibitors of farnesyl protein transferase from Artemisa argyi .  J Org Chem. 2002;  67 7670-5
  • 8 Seo J M, Kang H M, Son K H, Kim J H, Lee C W, Kim H M. et al . Antitumor activity of flavones isolated from Artimisia argyi .  Planta Med. 2003;  69 218-22
  • 9 Nagasuki T, Nakashima M, Koichiro K. Antimutagens in Gaiyou (Artemisia argyi Levl. et Vant.)  J Agric Food Chem. 2000;  48 3256-66
  • 10 Masayuki Y, Hiromi S, Hisashi M, Johji Y, Nobutoshi M. Bioactive constituents of Chinese natural medicines. I. New sesquiterpene ketones with vasorelaxant effect from Chinese Moxa, the processed leaves of Artemisia argyi Levl. et Vant.: moxartenone and moxartenolide.  Chem Pharm Bull. 1996;  44 1656-62
  • 11 Aoife L, O’Kennedy R. Studies on coumarins and coumarin-related compounds to determine their therapeutic role in the treatment of cancer.  Curr Pharm Design. 2004;  10 3797-811
  • 12 Liu X L, Zhang L, Fu X L, Chen K, Quian B C. Effect of scopoletin on PC3 cell proliferation and apoptosis.  Acta Pharmacol Sin. 2001;  22 929-33
  • 13 Kawaii S, Tomono Y, Ogawa K, Sugiura M, Yano M, Yoshizawa Y. The antiproliferative effect of coumarins on several cancer cell lines.  Anticancer Res. 2001;  21 917-23

Prof. Dr. Rudolf Bauer

Institut für Pharmazeutische Wissenschaften

Universitätsplatz 4

8010 Graz

Austria

Phone: +43-316-380-8700

Fax: +43-316-380-9860

Email: rudolf.bauer@uni-graz.at