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.
引用
收藏
页数:15
相关论文
共 99 条
  • [71] Pedras MSC, 2007, NAT PROD COMMUN, V2, P319
  • [72] Effcient synthesis of brussalexin A, a remarkable phytoalexin from Brussels sprouts
    Pedras, M. Soledade C.
    Zheng, Qing-An
    Sarwar, Mohammed G.
    [J]. ORGANIC & BIOMOLECULAR CHEMISTRY, 2007, 5 (08) : 1167 - 1169
  • [73] Phytoalexins from Brassicaceae: News from the front
    Pedras, M. Soledade C.
    Yaya, Estifanos E.
    [J]. PHYTOCHEMISTRY, 2010, 71 (11-12) : 1191 - 1197
  • [74] Metabolism and detoxification of phytoalexins and analogs by phytopathogenic fungi
    Pedras, MSC
    Ahiahonu, PWK
    [J]. PHYTOCHEMISTRY, 2005, 66 (04) : 391 - 411
  • [75] Phytoalexins from the crucifer rutabaga: Structures, syntheses, biosyntheses, and antifungal activity
    Pedras, MSC
    Montaut, S
    Suchy, M
    [J]. JOURNAL OF ORGANIC CHEMISTRY, 2004, 69 (13) : 4471 - 4476
  • [76] The synthesis and biosynthesis of phytoalexins produced by cruciferous plants
    Pedras, MSC
    Jha, M
    Ahiahonu, PWK
    [J]. CURRENT ORGANIC CHEMISTRY, 2003, 7 (16) : 1635 - 1647
  • [77] Phytoalexins from Thlaspi arvense, a wild crucifer resistant to virulent Leptosphaeria maculans:: structures, syntheses and antifungal activity
    Pedras, MSC
    Chumala, PB
    Suchy, M
    [J]. PHYTOCHEMISTRY, 2003, 64 (05) : 949 - 956
  • [78] Phytoalexins from crucifers: synthesis, biosynthesis, and biotransformation
    Pedras, MSC
    Okanga, FI
    Zaharia, IL
    Khan, AQ
    [J]. PHYTOCHEMISTRY, 2000, 53 (02) : 161 - 176
  • [79] Unprecedented chemical structure and biomimetic synthesis of erucalexin, a phytoalexin from the wild crucifer Erucastrum gallicum
    Pedras, MSC
    Suchy, M
    Ahiahonu, PWK
    [J]. ORGANIC & BIOMOLECULAR CHEMISTRY, 2006, 4 (04) : 691 - 701
  • [80] Cruciferous phytoalexins:: antiproliferative effects in T-Jurkat leukemic cells
    Pilátová, M
    Sarissky, M
    Kutschy, P
    Mirossay, A
    Mezencev, R
    Curillová, Z
    Suchy, M
    Monde, K
    Mirossay, L
    Mojzis, J
    [J]. LEUKEMIA RESEARCH, 2005, 29 (04) : 415 - 421