Three flavonoids, luteolin (1), vitexicarpin (2) and artemetin (3), from the salt marsh plant Vitex rotundifolia, were tested for their anti-proliferative activities in AGS, MCF-7 and HT-29 human cancer cell lines and compared with the control using MTT assay. Among them, 2 was most effective with an IC50 of 6.9 and 22.8 μM against AGS and HT-29 cells, respectively. In addition, mRNA expression levels of major apoptosis-related genes such as p21, p53, Bcl-2 and Bax in AGS cells were evaluated by reverse-transcription polymerase chain reaction (RT-PCR). Compound 2 not only enhanced most remarkably the expression level of tumor suppressor genes p53 and p21, and pro-apoptotic gene Bax at a concentration of 25 μM, but also suppressed the expression level of anti-apoptotic gene Bcl-2 to 20% at the same concentration, thus shifting the Bax/Bcl-2 ratio in favor of apoptosis.
CaoG., SoficE., PriorR.L. (1997) Antioxidant and prooxidant behavior of flavonoids: structure activity relationships. Free Radical Biology and Medicine, 22, 749–760; (b) Peterson J, Dwyer J. (1998) Flavonoids: dietary occurrence and biochemical activity. Nutrition Research, 18, 1995–2018; (c) Carlo GD, Mascolo N, Izzo AA, Capasso F. (1999) Flavonoids: old and new aspects of a class of natural therapeutic drugs. Life Sciences, 65, 337–353; (d) Pietta PG. (2000) Flavonoids as antioxidants. Journal of Natural Products, 63, 1035–1042; (e) Heim KE, Tagliaferro AR, Bobilya DJ. (2002) Flavonoid antioxidants: chemistry, metabolism and structure-activity relationships. The Journal of Nutritional Biochemistry, 13, 572–584; (f) Zhang S, Yang X, Coburn RA, Morris ME. (2005) Structure activity relationships and quantitative structure activity relationships for the flavonoid-mediated inhibition of breast cancer resistance protein. Biochemical Pharmacology, 70, 627–639.
2.
ScalbertA., WilliamsonG. (2000) Dietary intake and biovailability of polyphenols. Journal of Nutrition, 130, 2073S–2085S; (b) Vaouzour D, Vafeiadou K, Rodriguez-Mateos A, Rendeiro C, Spencer JPE. (2008) The neuroprotective potential of flavonoids: a multiplicity of effects. Genes and Nutrition, 3, 115–126; (c) Rathee P, Chaudhary H, Rathee S, Rathee D, Kumar V, Kohli K. (2009) Mechanism of action of flavonoids as anti-inflammatory agents: a review. Inflammation and Allergy Drug Targets, 8, 229–235.
3.
LeeY.N. (2002) Flora of Korea.Seoul, Korea: Kyo-Hak Publishing Co. Ltd.
4.
KondoY., SugiyamaK., NozoeS. (1986) Studies on the constituents of Vitex rotundifolia L. fil. Chemical & Pharmaceutical Bulletin, 34, 4829–4832; (b) Ono M, Ito Y, Kubo S, Nohara T. (1997) Two New Iridoids from Viticis trifoliae fructus (Fruit of Vitex rotundifolia L.). Chemical & Pharmaceutical Bulletin, 45, 1094–1096; (c) Ono M, Ito Y, Nohara T. (1998) A labdane diterpene glycoside from fruit of Vitex rotundifolia. Phytochemistry, 48, 207–209; (d) Ono M, Sawamura H, Ito Y, mMizuki K, Nohara T. (2000) Diterpenoids from the fruits of Vitex trifolia, Phytochemistry, 55, 873–877; (e) Ono M, Yamamoto M, Masuoka C, Ito Y, Yamashita M, Nohara T. (1999) Diterpenes from the fruits of Vitex rotundifolia. Journal of Natural Products, 62, 1532–1537; (f) Ono M, Ito Y, Nohara T. (2001) Four new halimane-type diterpenes, vitetrifolins D-G, from the fruit of Vitex trifolia. Chemical & Pharmaceutical Bulletin, 49, 1220–1222; (g) Ono M, Yamamoto M, Yanaka T, Ito Y, Nohara T. (2001) Ten new labdane-type diterpenes from the fruit of Vitex rotundifolia. Chemical & Pharmaceutical Bulletin, 49, 82–86; (h) You KM, Son KH, Chang HW, Kang SS, Kim HP. (1998) Vitexicarpin, a flavonoid from the fruits of Vitex rotundifolia, inhibits mouse lymphocyte proliferation and growth of cell lines in vitro. Planta Medica, 64, 546–550; (i) Kawazoe K, Yutani A, Takaishi Y. (1999) Aryl naphthalenes norlignans from Vitex rotundifolia. Phytochemistry, 52, 1657–1659; (j) Ko WG, Kang TH, Lee SJ, Kim NY, Kim YC, Sohn DH, Lee BH. (2000). Polymethoxyflavonoids from Vitex rotundifolia inhibit proliferation by inducing apoptosis in human myeloid leukemia cells. Food and Chemical Toxicology, 38, 861–865. (k) Ko WH, Kang TH, Lee SJ, Kim YC, Lee BH. (2001) Rotundifuran, a labdane type diterpene from Vitex rotundifolia, induces apoptosis in human myeloid leukaemia cells. Phytotherapy Research, 15, 535–537; (l) Shin TY, Kim SH, Lim JP, Suh ES, Jeong HJ, Kim BD, Park EJ, Hwang WJ, Rye DG, Baek SH, An NH, Kim HM. (2000) Effect of Vitex rotundifolia on immediate-type allergic reaction. Journal of Ethnopharmacology, 72, 443–450; (m) Wang HY, Cai B, Cui CB, Zhang DY, Yang BF. (2005) Vitexicarpin, a flavonoid from Vitex trifolia L., induces apoptosis in K562 cells via mitochondria-controlled apoptotic pathway. Yao Xue Xue Bao, 40, 27–31.
5.
KimY.A., LeeJ.I., KimH.J., KongC.S., NamT.J., SeoY. (2009) Antiproliferative effect of extracts, fractions and compound from Vitex rotundifolia on human cancer cells. Journal of Applied Biological Chemistry, 52, 180–186.
6.
IinumaM., MatsuuraS., KusudaK. (1980) 13C-Nuclear magnetic resonance (NMR) spectral studies on polysubstituted flavonoids. I. 13C-NMR spectra of flavones. Chemical & Pharmaceutical Bulletin, 28, 708–716; (b) Rahman AU, Ahmed D, Choudhary MI, Turkoz S, Sener B. (1988) Chemical constituents of Buxus sempervirens. Planta medica, 54, 173–174; (c) Ahmad VU, Khan MA, Baqai FT, Tareen RB. (1995) Santoflavone, a 5-deoxyflavonoid from Achillea santolina. Phytochemistry, 38, 1305–1307; (d) Yoshioka T, Inokuchi T, Fujioka S, Kimura Y. (2004). Phenolic compounds and flavonoids as plant growth regulators from fruit and leaf of Vitex rotundifolia. Zeitschrift Naturforschung, 59, 509–514; (e) Loizzo MR, Said A, Tundis R, Rashed K, Statti GA, Hufner A, Menichini1 F. (2007) Inhibition of angiotensin converting enzyme (ACE) by flavonoids isolated from Ailanthus excelsa (Roxb) (Simaroubaceae), Phytotherapy Research, 21, 32–36.
7.
WuB., ZhangQ., ShenW., ZhuJ. (2008) Anti-proliferative and chemosensitizing effects of luteolin on human gastric cancer AGS cell line, Molecular and Cellular Biochemistry, 313, 125–132.
8.
BeutlerJ.A., HamelE., VlietinckA.J., HaemersA., RajanP., RoitmanJ.N., CardellinaJ.H.II, BoydM.R. (1998) Structure-activity requirements for flavone cytotoxicity and binding to tubulinJournal of Medicinal Chemistry, 41, 2333–2338.
9.
MiyashitaT., KrajewkiS., KragewskaM., WangH.G., LinH.K., LiebermannD.A., HoffmanB., ReedJ.C. (1994) Tumor suppressor p53 is a regulator of bcl-2 and bax gene expression in vitro and in vivo. Oncogene, 9, 1799–1805; (b) Roy N, Deveraux OL, Takahashi R, Salvesen GS, Reed JC. (1997) The c-IAP-1 and c-IAP-2 proteins are direct inhibitors of specific caspases. The EMBO Journal, 16, 6914–6925; (c) Deveraux QL, Reed JC. (1999) IAP family proteins–suppressors of apoptosis. Genes & Development, 13, 239–252; (d) Gartel AL, Tyner AL. (2002). The role of the cyclin-dependent kinase inhibitor p21 in apoptosis. Molecular Cancer Therapeutics, 1, 639–649; (e) Khan N, Adhami VM, Mukhtar H. (2008) Apoptosis by dietary agents for prevention and treatment of cancer, Biochemical Pharmacology, 76, 1333–1339.
10.
KorsmeyerS.J., ShutterJ.R., VeisD.J., MerryD.E., OltvaiZ.N. (1993) Bcl-2/Bax: a rheostat that regulates an anti-oxidant pathway and cell death. Seminars in Cancer Biology, 4, 327–332.