Antiproliferative Effect of Indole Phytoalexins

被引:68
作者
Chripkova, Martina [1 ,2 ]
Zigo, Frantisek [3 ]
Mojzis, Jan [1 ]
机构
[1] Safarik Univ, Fac Med, Dept Pharmacol, Kosice 04011, Slovakia
[2] Univ Vet Med & Pharm, Dept Human & Clin Pharmacol, Kosice 04011, Slovakia
[3] Univ Vet Med & Pharm, Dept Anim Breeding, Kosice 04011, Slovakia
关键词
indole phytoalexins; crucifers; brassinin; antiproliferative; cancer; PROSTATE-CANCER CELLS; DIETARY PHENETHYL ISOTHIOCYANATE; POTENTIAL ANTICANCER AGENTS; DITHIOCARBAMATE SIDE-CHAINS; CRUCIFEROUS PHYTOALEXINS; IN-VITRO; 4(3H)-QUINAZOLINONE DERIVATIVES; CHEMOPREVENTIVE ACTIVITY; ANTIFUNGAL ACTIVITY; BIOLOGICAL-ACTIVITY;
D O I
10.3390/molecules21121626
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Indole phytoalexins from crucifers have been shown to exhibit significant anti-cancer, chemopreventive, and antiproliferative activity. Phytoalexins are natural low molecular antimicrobial compounds that are synthesized and accumulated in plants after their exposure to pathogenic microorganisms. Most interestingly, crucifers appear to be the only plant family producing sulfur-containing indole phytoalexins. The mechanisms underlying its anti-cancer properties are unknown. Isolation from cruciferous plants does not provide sufficient quantities of indole phytoalexins and, for biological screening, they are usually obtainable through synthesis. Understanding the molecular mechanism of the action of these substances and their structure-activity relationships is quite important in the development of new analogs with a more favorable profile of biological activities. In this review, we present the key features of indole phytoalexins, mainly their antiproliferative ativities.
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页数:15
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共 99 条
  • [1] In vivo anti-tumor activity of a novel indolocarbazole compound, J-107088, on murine and human tumors transplanted into mice
    Arakawa, H
    Morita, M
    Kodera, T
    Okura, A
    Ohkubo, M
    Morishima, H
    Nishimura, S
    [J]. JAPANESE JOURNAL OF CANCER RESEARCH, 1999, 90 (10): : 1163 - 1170
  • [2] Bacher G, 2001, CANCER RES, V61, P392
  • [3] Bailey J. A., 1982, PHYTOALEXINS
  • [4] A key in vivo antitumor mechanism of action of natural product-based brassinins is inhibition of indoleamine 2,3-dioxygenase
    Banerjee, T.
    DuHadaway, J. B.
    Gaspari, P.
    Sutanto-Ward, E.
    Munn, D. H.
    Mellor, A. L.
    Malachowski, W. P.
    Prendergast, G. C.
    Muller, A. J.
    [J]. ONCOGENE, 2008, 27 (20) : 2851 - 2857
  • [5] Benzyl Isothiocyanate Suppresses Pancreatic Tumor Angiogenesis and Invasion by Inhibiting HIF-α/VEGF/Rho-GTPases: Pivotal Role of STAT-3
    Boreddy, Srinivas Reddy
    Sahu, Ravi P.
    Srivastava, Sanjay K.
    [J]. PLOS ONE, 2011, 6 (10):
  • [6] Chemistry and neurochemistry of the kynurenine pathway of tryptophan metabolism
    Botting, NP
    [J]. CHEMICAL SOCIETY REVIEWS, 1995, 24 (06) : 401 - &
  • [7] Brooks JD, 2001, CANCER EPIDEM BIOMAR, V10, P949
  • [8] The synthesis and anticancer activity of analogs of the indole phytoalexins brassinin, 1-methoxyspirobrassinol methyl ether and cyclobrassinin
    Budovska, Mariana
    Pilatova, Martina
    Varinska, Lenka
    Mojzis, Jan
    Mezencev, Roman
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY, 2013, 21 (21) : 6623 - 6633
  • [9] Buettner R, 2002, CLIN CANCER RES, V8, P945
  • [10] Synthesis and in vitro antitumor activity of 4(3H)-quinazolinone derivatives with dithiocarbamate side chains
    Cao, SL
    Feng, YP
    Jiang, YY
    Liu, SY
    Ding, GY
    Li, RT
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2005, 15 (07) : 1915 - 1917