Cytotoxic compounds from Annonaceus species as DNA topoisomerase I poisons

被引:0
|
作者
López-Lázaro, M
Martín-Cordero, C
Bermejo, A
Cortes, D
Ayuso, MJ
机构
[1] Univ Sevilla, Fac Farm, Dept Farmacol, E-41012 Seville, Spain
[2] Univ Valencia, Fac Farm, Dept Farmacol, E-46100 Valencia, Spain
关键词
Annonaceae; acetogenin; styryl-lactones; topoisomerase; SRB;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: In the search for cytotoxic natural products as DNA topoisomerase poisons, we have assessed six annonaceus compounds (the acetogenins annonacin and rolliniastatin-1, the styryl-lactones etharversin and altholactone and the alkaloids thaligrisine and cepharanone-B) for cytotoxic activity against three human cancer cell lines and then we evaluated these compounds as DNA topoisomerase poisons. Materials and Methods: The cytotoxicity parameters were determined following protocols established by the National Cancer Institute (NCI) using the SRB assay. In the topoisomerase assay, the supercoiled DNA produces open circle forms that are stabilised in the presence of DNA topoisomerase poisons and can be detected after a denaturation step by proteinase K-SDS. Results: The six compounds showed cytotoxic activity, with cepharanone B being the most cytotoxic one, even more than the antineoplastic agent etoposide on two cancer cell lines, although it is the only one that does not act as a DNA topoisomerase poison. Conclusion: These results could justify the traditional use of the studied annonaceus species and topoisomerase-mediated DNA damage might be a possible mechanism by which five of these compounds exert their cytotoxicity.
引用
收藏
页码:3493 / 3497
页数:5
相关论文
共 50 条
  • [1] Synthesis of cytotoxic indenoisoquinoline topoisomerase I poisons
    Strumberg, D
    Pommier, Y
    Paull, K
    Jayaraman, M
    Nagafuji, P
    Cushman, M
    JOURNAL OF MEDICINAL CHEMISTRY, 1999, 42 (03) : 446 - 457
  • [2] Iridoids as DNA topoisomerase I poisons
    Gálvez, M
    Martín-Cordero, C
    Ayuso, MJ
    JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY, 2005, 20 (04) : 389 - 392
  • [3] Flavonoids as DNA topoisomerase I poisons
    López-Lázaro, M
    Martín-Cordero, C
    Toro, MV
    Ayuso, MJ
    JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY, 2002, 17 (01) : 25 - 29
  • [4] Coralyne and related compounds as mammalian topoisomerase I and topoisomerase II poisons
    Makhey, D
    Gatto, B
    Yu, CA
    Liu, A
    Liu, LF
    LaVoie, EJ
    BIOORGANIC & MEDICINAL CHEMISTRY, 1996, 4 (06) : 781 - 791
  • [5] Targeting DNA Topoisomerase I with Non-Camptothecin Poisons
    Beretta, G. L.
    Zuco, V.
    Perego, P.
    Zaffaroni, N.
    CURRENT MEDICINAL CHEMISTRY, 2012, 19 (08) : 1238 - 1257
  • [6] Calothrixins, a New Class of Human DNA Topoisomerase I Poisons
    Khan, Qasim A.
    Lu, Jun
    Hecht, Sidney M.
    JOURNAL OF NATURAL PRODUCTS, 2009, 72 (03): : 438 - 442
  • [7] Two new flavonol glycosides as DNA topoisomerase I poisons
    López-Lázaro, M
    Martín-Cordero, C
    Ayuso, MJ
    ZEITSCHRIFT FUR NATURFORSCHUNG SECTION C-A JOURNAL OF BIOSCIENCES, 2000, 55 (11-12): : 898 - 902
  • [8] UBC9 functions to protect cells from DNA topoisomerase I poisons
    Jacquiau, HR
    van Waardenburg, RCAM
    Reid, RJD
    Bjornsti, MA
    YEAST, 2003, 20 : S113 - S113
  • [9] DNA topoisomerase I inhibitors: Cytotoxic flavones from Lethedon tannaensis
    Zahir, A
    Jossang, A
    Bodo, B
    Provost, J
    Cosson, JP
    Sevenet, T
    JOURNAL OF NATURAL PRODUCTS, 1996, 59 (07): : 701 - 703
  • [10] Novel genes affecting cell sensitivity to DNA topoisomerase I poisons
    Reid, RJD
    Fiorani, P
    Bjornsti, MA
    ANNALS OF ONCOLOGY, 1998, 9 : 58 - 58